WO2007043835A1 - Fab i inhibitor and process for preparing same - Google Patents

Fab i inhibitor and process for preparing same Download PDF

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Publication number
WO2007043835A1
WO2007043835A1 PCT/KR2006/004133 KR2006004133W WO2007043835A1 WO 2007043835 A1 WO2007043835 A1 WO 2007043835A1 KR 2006004133 W KR2006004133 W KR 2006004133W WO 2007043835 A1 WO2007043835 A1 WO 2007043835A1
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WIPO (PCT)
Prior art keywords
pyridin
benzyl
pentyloxy
methyl
dichloro
Prior art date
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Ceased
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PCT/KR2006/004133
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French (fr)
Inventor
Cheol Min Kim
Young Lan Hyun
Dong Kyu Shin
Seonggu Ro
Joong Myung Cho
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CrystalGenomics Inc
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CrystalGenomics Inc
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Filing date
Publication date
Application filed by CrystalGenomics Inc filed Critical CrystalGenomics Inc
Priority to EP06799211.5A priority Critical patent/EP1948601B1/en
Priority to CN2006800378269A priority patent/CN101282930B/en
Priority to BRPI0617268-7A priority patent/BRPI0617268A2/en
Priority to KR1020147004300A priority patent/KR101522713B1/en
Priority to ES06799211.5T priority patent/ES2576579T3/en
Priority to CA2625962A priority patent/CA2625962C/en
Priority to KR1020087011392A priority patent/KR101502335B1/en
Priority to JP2008535461A priority patent/JP5049977B2/en
Publication of WO2007043835A1 publication Critical patent/WO2007043835A1/en
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

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    • C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D213/62—Oxygen or sulfur atoms
    • C07D213/63—One oxygen atom
    • C07D213/64—One oxygen atom attached in position 2 or 6
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    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
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    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
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    • A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/50—Pyridazines; Hydrogenated pyridazines
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    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
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    • C07D237/10—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
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    • C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
    • C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
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    • C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
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    • C07D401/06—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
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    • C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
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Definitions

  • the present invention relates to a novel compound for inhibiting Fab I involved in bacterial fatty acid biosynthesis.
  • This application claims priority under 35 U.S.C. 119(e) to the Provisional application filed on October 13, 2005 entitled “Novel Fab I Inhibitor And Process For Preparing Same," and to Provisional application 60/827,029 filed on September 26, 2006, both of which are hereby incorporated by reference.
  • DESCRIPTION OF THE PRIOR ART Fatty acid synthase (FAS) is involved in the overall biosynthetic pathway of saturated fatty acids in all organisms, but the structural organization of FAS varies considerably among them.
  • FAS acyl carrier protein
  • NADH-dependent enoyl-ACP reductase (Fab I) is involved in the last step of the four reaction steps involved in each cycle of bacterial fatty acid biosynthesis. (See Payne et al, Drug Discovery Today 6, 2001, 537-544).
  • the first step the condensation of malonyl-ACP with acetyl-CoA (Fab H), is catalyzed by ⁇ -ketoacyl-ACP synthase.
  • the second step is ketoester reduction by NADPH-dependent ⁇ -ketoacyl-ACP reductase (Fab G). Subsequent dehydration by ⁇ -hydroxyacyl-ACP dehydrase (Fab A or Fab Z) leads to trans-2-enoyl-ACP.
  • trans-2-enoyl-ACP is converted to acyl-ACP having two additional carbon atoms by Fab I.
  • Fab I is the biosynthetic enzyme in the overall synthetic pathway of bacterial fatty acid biosynthesis.
  • Fab I is the target for a broad spectrum antibacterial agent such as triclosan (see McMurry et al., Nature, 1998, 394, 531-532) or diazaborine (see Baldock et al., Science, 1996, 274, 2107-2110). Also, diazaborine has been reported to function as an irreversible inhibitor of Fab I through the formation of a covalent complex with Fab I (see Baldock et al., Biochem. Pham. 1998, 55, 1541-1549), while triclosan is a reversible inhibitor of Fab I (see Ward et al., Biochem. 38, 12514- 12525).
  • B is H, C 1-4 alkyl or C 3-6 cycloalkyl
  • D is H or Ci -4 alkyl
  • E is CH 2 when the bond to which it is attached is a double bond; or E is H or C 1 .4 alkyl when the bond to which it is attached is a single bond, in which A is H or C 1-4 alkyl; F is H or C 1-4 alkyl; G is H, C 1-4 alkyl or Co -6 alkylaryl; I is O orN R' 2 ;
  • X is each independently H, C 1-4 alkyl, CH 2 OH, OR', SR', CN, N(RZ) 2 , CH 2 N(R') 2 , NO 2 , CF 3 , CO 2 R', CON(RZ) 2 , COR', F, Cl 5 Br 5 1 or -S(O) r CF 3 (r is O, 1 or
  • R ' is each independently H 5 Ci -4 alkyl or C 0-6 alkylaryl.
  • the present inventors have developed a novel Fab I inhibitor which has broad antibacterial activity against Gram positive bacteria including methicillin resistant Staphylococcus Aureus (MRSA).
  • MRSA methicillin resistant Staphylococcus Aureus
  • Ri is selected from the group of radicals consisting of:
  • R 4 is selected from the group of radicals consisting of:
  • Ci -8 alkyl Ci -8 alkenyl, Cj -8 alkynyl,
  • W is selected from the group consisting of C-R 6 and N;
  • Z is selected from the group consisting of C-R 5 and N;
  • R 5 and R 6 are each independently selected from the group consisting of H, halogen, C 1-5 alkyl, and substituted C 1-5 alkyl containing one or more substituents selected from the group consisting of methyl, ethyl, hydroxyl, hydroxylmethyl and hydroxylethyl; and X is selected from C, N, O and S.
  • heteroaryl as used herein means an aryl group containing one or more heteroatoms selected from N, S or O in the ring structure.
  • exemplary heteroaryls include those derived from pyrrole, pyrazole, imidazole, 1,2,3-triazole, 1,2,4-triazole, furan, isoxazole, oxazole, thiophene, isothiazole, thiazolidine, thiazole, 1,2,5-oxadiazole, 1,2,3- oxadiazole, 1,2,5-thiodiazole, 1,2,3-thiodiazole, 1,3,4-oxadiazole, 1,3,4-thiodiazole, pyridine, pyrimidine, tetrazole and triazine.
  • bacteria-related diseases means illnesses or conditions which are caused by bacterial infection and may be alleviated or relieved by a Fab I inhibitor treatment, and may include but are not limited to urinary tract, respiratory or skin tissue infections, sepsis, etc.
  • inventive compound may contain asymmetric centers of R or S configuration and thus the present invention includes geometrical isomers, stereoisomers and racemic mixtures of the compound of formula (I) or (II).
  • the pharmaceutically acceptable salt of the inventive compound which may be a non-toxic addition salt may be prepared by using an acid or base.
  • Exemplary acids which may be used in the present invention include such inorganic acids as hydrochloric, hydrobromic, phosphoric and sulfuric acid; and an organic acid such as an organic carboxylic acid, e.g., acetic, trifluoroacetic, citric, formic, maleic, oxalic, succinic, benzoic, tartaric, fumaric, mandelic, ascorbic and malic acid, methanesulfonic acid and /?-toluenesulfonic acid.
  • organic carboxylic acid e.g., acetic, trifluoroacetic, citric, formic, maleic, oxalic, succinic, benzoic, tartaric, fumaric, mandelic, ascorbic and malic acid, methanesulfonic acid and /?-toluenesulfonic acid.
  • Exemplary bases which may be used in the present invention include such inorganic bases as an alkali metal hydroxide (e.g., sodium hydroxide and potassium hydroxide), an alkali metal bicarbonate (e.g., sodium bicarbonate and potassium bicarbonate), an alkali metal carbonate (e.g., sodium carbonate, potassium carbonate and calcium carbonate) and an organic base such as amines.
  • alkali metal hydroxide e.g., sodium hydroxide and potassium hydroxide
  • an alkali metal bicarbonate e.g., sodium bicarbonate and potassium bicarbonate
  • an alkali metal carbonate e.g., sodium carbonate, potassium carbonate and calcium carbonate
  • organic base such as amines.
  • the inventive compound may also be used in the form of a pharmaceutically acceptable derivative or prodrug which has a suitable ester or amide group.
  • ester which can be hydrolyzed chemically or biochemically in the living body include indanyl, phthalidyl, pivaloyloxymethyl, glycyloxymethyl, phenylglycyloxymethyl, and 5-methyl-2-oxo-l,3-dioxorene-4-ylmethyl esters.
  • the preferred compounds of the present invention are as follows:
  • the compound of formula (I) or (II) may be prepared by simple alkylation or arylation using pyridazine derivative, pyrimidinone derivative, triazinone derivative or pyridone derivative.
  • a preferred example of the compound of formula (I) is a pyridone compound which may be prepared as shown in Reaction Scheme 1 or 2.
  • NaH sodium hydride
  • TsCl is p-toluenesulfonyl chloride
  • Ac 2 O is acetic anhydride
  • BuOH is butanol
  • t-BuOH is t-butanol
  • Pd/C palladium on carbon
  • KOtBu potassium t- butoxide
  • Zn zinc dust.
  • Another preferred example of the compound of formula (I) is a pyridone compound being substituted with a methyl group, which may be prepared as shown in Reaction Scheme 5.
  • Reagents (a) NaH 1 pentyl bromide, DMF; (b) benzyl amine, EtOH, reflux Still another preferred example of the compound of formula is a pyridazine compound, which may be prepared as shown in Reaction Scheme 6.
  • the compound of formula (I) or (II) effectively inhibits the activity of Fab I.
  • the present invention provides a method for inhibiting the activity of Fab I, comprising bringing a body fluid such as blood, urine and lymph into contact with the compound of formula (I) or (II).
  • the present invention also provides a pharmaceutical composition
  • a pharmaceutical composition comprising the compound of formula (I) or (II) as an active ingredient in an amount effective to treat or prevent bacteria-related diseases.
  • the inventive pharmaceutical composition may comprise pharmaceutically acceptable carriers, diluents, adjuvants or vehicles.
  • Exemplary carriers, diluents, adjuvants and vehicles include, but are not limited to, ion exchangers, alumina, aluminum stearate, lecithin, serum proteins such as human serum albumin, buffer substances such as phosphates, glycine, sorbic acid, potassium sorbate, partial glyceride mixtures of saturated vegetable fatty acids, water, salts or electrolytes such as protamine sulfate, disodium hydrogen phosphate, potassium hydrogen phosphate, sodium chloride or zinc salts, colloidal silica, magnesium trisilicate, polyvinyl pyrrolidone, cellulose-based substances, polyethylene glycol, sodium carboxy methylcellulose, polyacrylates, waxes, polyethylene-polyoxypropylene-block polymers, polyethylene glycol, wool fat, parabens, chlorobutanol, phenol, sorbic acid, aluminum monostearate, gelatin and the like. It may also be desirable to include isotonic agents, for example
  • compositions of the present invention may be prepared using surfactants such as TWEENsTM or SPANsTM, emulsifying agents, extenders, etc., and may be administered orally, sublingualis parenterally, by inhalation spray, topically, rectally, nasally, buccally, vaginally or via an implanted reservoir.
  • parenteral as used herein includes subcutaneous, intravenous, intramuscular, intra-articular, intra- synovial, intrasternal, intrathecal, intrahepatic, intralesional and intracranial injection or infusion techniques.
  • the composition is administered orally, intraperitoneally, subcutaneously, intramuscularly or intravenously.
  • Sterile injectable formulations may be in the form of aqueous or oleaginous suspensions. These suspensions may be formulated by a conventional method using suitable dispersing or wetting agents and suspending agents such as water, ethanol, polyols (propyleneglycol, polyethyleneglycol, glycerol, and the like), suitable mixtures thereof, vegetable oils (such as olive oil), and injectable organic esters such as ethyl oleate. Proper fluidity can be maintained, for example, by the use of a coating such as lecithin, by the maintenance of the required particle size in the case of dispersions and by the use of surfactants.
  • suitable dispersing or wetting agents and suspending agents such as water, ethanol, polyols (propyleneglycol, polyethyleneglycol, glycerol, and the like), suitable mixtures thereof, vegetable oils (such as olive oil), and injectable organic esters such as ethyl oleate.
  • Formulations suitable for oral administration may be in the form of capsules, tablets, pills, powders, or granules.
  • the active compound can be admixed with at least one inert carrier such as sodium citrate or dicalcium phosphate; or with fillers, extenders, binders, humectants, disintegrating agents such as calcium carbonate or certain complex silicates, solution retarders such as paraffin, absorption accelerators such as quaternary ammonium compounds, wetting agents such as cetyl alcohol or glycerol monostearate, adsorbents, and lubricants such as magnesium stearate, solid polyethylene glycols, and the like, or mixtures thereof.
  • inert carrier such as sodium citrate or dicalcium phosphate
  • the active compound in the form of capsules, can be admixed with buffering agents, and can also be admixed with excipients such as lactose or milk sugar as well as high molecular weight polyethyleneglycols, and the like.
  • Formulations suitable for oral administration may alternatively be in the form of aqueous suspensions, solutions, syrups, etc.
  • aqueous suspensions When aqueous suspensions are required for oral use, the active ingredient is combined with emulsifying and suspending agents. If desired, certain sweetening, flavoring or coloring agents may also be added.
  • Formulations for oral administration can include a coating, and can be formulated with certain agents so as to release the active compound in a particular portion of the digestive tract.
  • Formulations for topical administration may be useful in that the target of treatment includes areas or organs readily accessible by topical application, e.g., the eye, the skin or the lower intestinal tract.
  • Topically-transdermal patches may also be used for topical administration.
  • the compositions may be formulated in the form of ointments, lotions, creams or sprays form containing the active component suspended or dissolved in one or more suitable carriers.
  • the ointments may contain mineral oil, liquid petrolatum, white petrolatum, propylene glycol, polyoxyethylene, polyoxypropylene, emulsifying wax or water as suitable carriers.
  • the lotions, creams or sprays may contain mineral oil, sorbitan monostearate, polysorbate 60, cetyl esters wax, cetearyl alcohol, 2-octyldodecanol, benzyl alcohol or water as suitable carriers.
  • the compositions may be formulated as micronized suspensions or solutions in isotonic, pH adjusted sterile saline, either with or without a preservative such as benzylalkonium chloride.
  • the compositions may be formulated in ophthalmic ointments such as petrolatum.
  • Formulations suitable for administration by nasal aerosol or inhalation may be in the form of solutions in saline.
  • the solutions may contain benzyl alcohol or other suitable preservatives, absorption promoters to enhance bioavailability, fluorocarbons, and/or other conventional solubilizing or dispersing agents.
  • Formulations suitable for rectal or vaginal administration can be prepared by mixing the compounds of the present invention with suitable non-irritating excipients or carriers such as a suppository wax, cocoa butter, or polyethyleneglycol which melt at body temperature.
  • suitable non-irritating excipients or carriers such as a suppository wax, cocoa butter, or polyethyleneglycol which melt at body temperature.
  • inventive compound may be used with other antimicrobials such as penicillin or cephalosporin.
  • a single dose of the compound of formula (I) or (II) may range from about 50 to 1,500 mg, although the dose may be varied depending upon the age, body weight and symptoms of the patient.
  • a typical daily dose of the compound of formula (I) or (II) may range from about 50 to 5,000 mg, or from about 150 to 3,000 mg for adults, and can be from about 50 to 2000 mg, or from about 100 to 2000 mg, or from about 300 to 2500 mg, or from about 500 to 4000 mg, or from about 500 to 5000 mg.
  • the present invention provides a method for treating bacteria-related diseases, comprising administering an effective amount of a compound of formula (I) or (II) to a patient in need of such treatment.
  • the patient to be treated by the above method may include a human or non-human mammalian.
  • Example 2 to 13 The procedure of Example 1 was repeated except the starting material to obtain the titled compound.
  • Example 2 4-benzyloxy-l ⁇ (4-chloro-benzyl)-lH-pyridin-2-one 1 H NMR (CDCl 3 , 300 MHz) ⁇ 4.96 (s, 2H) 5 5.01 (s, 2H), 5.93 (dd, IH) 5 5.99 (d, IH) 5 7.09 (d, IH) 5 7.19 (d, 2H) 5 7.24 (d, 2H) 5 7.28-7.36 (m, 5H)
  • Example 3 4-benzyloxy-l-(4-nitro-benzyl)-lH-pyridin-2-one 1 B. NMR (CDCl 35 300 MHz) ⁇ 5.08 (s, 2H), 5.47 (s, 2H), 6.39-6.60 (m, 2H), 7.35-7.59 (m, 7H) 5 7.95 (d, IH), 8.18-8.23 (m, 2H)
  • Example 8 4-benzyloxy-2-(4-methyl-benzyloxy)-pyridine 1 H NMR (CDCl 3 , 300 MHz) ⁇ 2.37 (s, 3H), 5.06 (s, 2H), 5.33 (s, 2H), 6.34 (d, IH), 6.56 (dd, IH), 7.19 (d, 2H), 7.34-7.41 (m, 7H), 8.00 (d, IH)
  • Example 9 4-benzyloxy-l-(4-methyl-benzyl)-lH-pyridin-2-one 1 H NMR (CDCl 3 , 300 MHz) ⁇ 2.33 (s, 3H), 4.98 (s, 2H), 5.04 (s, 2H), 5.93 (dd, IH), 6.02 (d, IH), 7.10-7.19 (m, 5H), 7.34-7.38 (m, 5H)
  • Example 15 3-benzyl-l-(2,4-dichloro-benzyl)-4-hydroxy-lH-pyridin-2-one l-(2,4-dichloro-benzyl)-4-hydroxy-lH-pyridin-2-one synthesized in Example 14 was dissolved in DMF followed by adding NaH and benzyl bromide to obtain 4- benzyloxy-l-(2,4-dichloro-benzyl)-lH-pyridin-2-one and the titled compound in the ratio of 1 : 1.
  • Example 16 to 225 The procedure of Example 1 was repeated except the starting material to obtain the titled compound.
  • Example 16 4-(biphenyl-4-ylmethoxy)- 1 -(2,4-dichloro-benzyl)- 1 H-pyridin-2-one 1 H NMR (CDCI 3 , 300 MHz) ⁇ 5.04 (s, 2H), 5.15 (s, 2H), 6.01 (dd, IH), 6.06 (d, IH) 5 7.22-7.63 (m, 13H)
  • Example 17 1 -(2,4-dichloro-benzyl)-4-(2,4-dichloro-benzyloxy)-lH-pyridin-2-one 1 H NMR (CDCl 3 , 300 MHz) ⁇ 5.06 (s, 2H), 5.15 (s, 2H), 5.99-6.01 (m, 2H), 7.15-7.44 (m, 7H)
  • Example 18 4-(2-chloro-benzyloxy)- 1 -(2,4-dichloro-benzyl)- 1 H-pyridin-2-one 1 H NMR (CDCl 3 , 300 MHz) ⁇ 5.11 (s, 2H) 5 5.16 (s, 2H) 5 6.00-6.04 (m, 2H) 5 7.21-7.47 (m, 8H)
  • Example 21 4-cyclohexylmethoxy- 1 -(2,4-dichloro-benzyl)- 1 H-pyridin-2-one 1 H NMR (CDCl 3 , 300 MHz) ⁇ 0.86-1.83 (m, HH), 3.71 (d, 2H), 5.14 (s, 2H), 5.90-5.94 (m, 2H) 5 7.15-7.23 (m, 3H), 7.40 (s, IH)
  • Example 26 l-(2,4-dichloro-benzyl)-4-octyloxy-l H-pyridin-2-one 1 H NMR (CDCl 3 , 300 MHz) ⁇ 0.84 (t, 3H), 1.24-1.52 (m, 10H), 1.67-1.76 (m, 2H), 3.86 (t, 2H), 5.09 (s, 2H), 5.86-5.89 (m, 2H), 7.10-7.18 (m, 3H), 7.36 (s, IH)
  • Example 27 1 -(2,4-dichloro-benzyl)-4-(4-methyl-pentoxy)-l H-pyridin-2-one 1 H NMR (CDCl 3 , 300 MHz) ⁇ 0.86 (d, 6H), 1.24-1.29 (m, 2H), 1.50-1.59 (m, IH), 1.67- 1.77 (m, 2H), 3.86 (t, 2H), 5.10 (s, 2H), 5.87-5.90 (m, 2H), 7.11-7.16 (m, 3H), 7.36 (s, IH)
  • Example 28 4-(but-3-enyIoxy)-l-(2,4-dichloro-benzyl)-lH-pyridin-2-one 1 H NMR (CDCl 3 , 300 MHz) ⁇ 2.48 (q, 2H), 3.93 (t, 2H), 5.06-5.15 (m, 4H), 5.76-5.89 (m, 3H), 7.11-7.15 (m, 3H), 7.36 (s, IH)
  • Example 34 l-(2-chloro-benzyl)-4-pentyloxy-l H-pyridin-2-one 1 U NMR (CDCl 3 , 300 MHz) ⁇ 0.92 (t, 3H) 5 1.31-1.42 (m, 4H), 1.72-1.79 (m, 2H), 3.91 (t, 2H), 5.19 (S, 2H), 5.89-5.92 (m, 2H) 5 7.14-7.26 (m, 4H), 7.37-7.40 (m, IH)
  • Example 40 l-(2,4-dichloro-benzyl)-4-heptoxy-lH-pyridin-2-one 1 H NMR (CDCl 3 , 300 MHz) ⁇ 0.75 (t, 3H), 1.09-1.54 (m, 8H), 1.71-1.80 (m, 2H), 3.91 (t, 2H), 5.13 (s, 2H), 5.86-5.92 (m, 2H), 7.14-7.22 (m, 3H), 7.40 (s, IH)
  • Example 42 4-aryloxy-l-(2,4-dichloro-benzyl)-lH-pyridin-2-one 1 H NMR (CDCl 35 300 MHz) ⁇ 4.48 (d, 2H) 5 5.14 (s, 2H), 5.32-5.45 (m, 2H), 5.94-6.07 (m, 3H) 5 7.18-7.20 (m, 3H), 7.41 (s, IH)
  • Example 43 1 -(2,4-dichloro-benzyl)-4-(3-methoxy-propoxy)-lH-pyridin-2-one 1 H NMR (CDCl 35 300 MHz) ⁇ 2.01-2.07 (m, 2H) 5 3.35 (s, 3H) 5 3.52 (t, 2H), 4.02 (t, 2H) 5 5.14 (s, 2H) 5 5.91-5.94 (m, 2H), 7.16-7.20 (m, 3H) 5 7.41 (s, IH)
  • Example 46 l-(3-methyl-but-2-enyl)-4-pentyloxy-l H-pyridin-2-one 1 H NMR (CDCl 3 , 300 MHz) ⁇ 0.92 (t, 3H) 5 1.33-1.38 (m, 4H) 5 1.71-1.73 (m, 2H), 1.76 (s, 6H) 5 3.89 (t, 2H) 5 4.47 (d, 2H), 5.27 (t, IH) 5 5.87-5.88 (m, 2H) 5 7.10-7.13 (m, IH)
  • Example 47 5-(2-oxo-4-pentyloxy-2H-pyridin-l-ylmethyl)-furan-2-carboxyl acid ethylester 1 H NMR (CDCl 3 , 300 MHz) ⁇ 0.92 (t, 3H), 1.33-1.44 (m, 7H), 1.73-1.80 (m, 2H), 3.89 (t, 2H), 4.34 (q, 2H), 5.09 (s, 2H), 5.86 (d, IH), 5.92 (dd, IH), 6.47 (d, IH), 7.09 (d, IH), 7.29 (d, IH)
  • Example 49 4-pentyloxy-l-thiazol-4-ylmethyl-lH-pyridin-2-one 1 H NMR (CDCl 3 , 300 MHz) ⁇ 0.92 (t, 3H), 1.32-1.44 (m, 4H), 1.70-1.80 (m, 2H), 3.89 (t, 2H), 5.22 (s, 2H), 5.88 (d, IH), 5.92 (dd, IH), 7.38-7.42 (m, 2H), 8.76 (s, IH)
  • Example 50 4-pentyloxy-l-pyridin ⁇ 3-ylmethyl-lH-pyridin-2-one 1 H NMR (CDCl 3 , 300 MHz) ⁇ 0.93 (t, 3H), 1.32-1.45 (m, 4H), 1.74-1.83 (m, 2H), 3.96 (t, 2H), 5.55 (s, 2H), 6.29 (d, IH), 6.50 (dd, IH) 5 7.40 (s, IH), 7.96 (d, IH) 5 8.84 (d, IH)
  • Example 51 l-(2,4-dichloro-benzyl)-4-(4-methyl-pent-3-enyloxy)-lH-pyridin-2-one 1 H NMR (CDCl 3 , 300 MHz) ⁇ 1.65 (s, 3H), 1.73 (s, 3H), 2.46 (q, 2H), 3.89 (t, 2H) 5 5.14 (s 5 2H) 5 5.91-5.94 (m, 2H), 7.15-7.13 (m, 3H), 7.27 (s, IH) 5 7.41 (s, IH)
  • Example 52 l-(2,4-dichloro-benzyl)-4-(3-methoxy-propoxy)-lH-pyridin-2-one 1 H NMR (CDCl 3 , 300 MHz) ⁇ 0.88 (d, 6H) 5 1.18-1.26 (m, 4H), 1.37-1.77 (m, 5H) 5 3.92 (t, 2H) 5 5.14 (s, 2H), 5.91-5.93 (m, 2H) 5 7.15-7.23 (m, 3H) 5 7.41 (s, IH)
  • Example 53 1 -(2,4-dichloro-benzyl)-4-phenetyloxy- 1 H-pyridin-2-one
  • Example 57 1 -(3 ,4-dichloro-benzyl)-4-pentyloxy- 1 H-pyridin-2-one 1 H NMR (CDCI 3 , 300 MHz) ⁇ 0.93 (t, 3H) 5 1.31-1.46 (m, 4H), 1.73-1.82 (m, 2H) 5 3.92 (t, 2H) 5 5.02 (s, 2H) 5 5.92-5.95 (m, 2H) 5 7.10-7.15 (m, 2H) 5 7.36-7.42 (m, 2H)
  • Example 58 1 -(3 ,4-difluoro-benzyl)-4-pentyloxy-l H-pyridin-2-one
  • Example 59 4-(4-benzyloxy-butoxy)-l-(2,4-dichloro-benzyl)-lH-pyridin-2-one 1 H NMR (CDCl 3 , 300 MHz) ⁇ 1.68-1.94 (m. 4H), 3.54 (t, 2H) 5 3.96 (t, 2H) 5 4.53 (s, 2H), 5.15 (s, 2H), 5.90-5.93 (m, 2H), 7.16-7.42 (m, 9H)
  • Example 60 1 -(2,4-dichloro-benzyl)-4-(4-hydroxy-butoxy)-lH-pyridin-2-one 1 H NMR (CDCl 3 , 300 MHz) ⁇ 1.70-1.91 (m, 4H), 3.72 (t, 2H), 3.98 (t, 2H), 5.14 (s, 2H), 5.92-5.94 (m, 2H), 7.16-7.25 (m, 3H) 5 7.41 (s, IH)
  • Example 63 l-(6-chloro-benzo[l,3]dioxol-5-ylmethyl)-4-pentyloxy-lH-pyridin-2-one 1 H NMR (CDCl 3 , 300 MHz) ⁇ 0.93 (t, 3H), 1.35-1.43 (m, 4H), 1.74-1.79 (m, 2H), 3.91 (t, 2H), 5.10 (s, 2H), 5.88-5.91 (m, 2H), 5.96 (s, 2H), 6.81 (s, IH), 6.84 (s, IH), 7.18 (dd, IH)
  • Example 64 l-(2,4-dichloro-benzyl)-4-(2-m ethyl -benzyloxy)-lH-pyridin-2-one 1 H NMR (CDCl 3 , 300 MHz) ⁇ 2.35 (s, 3H) 5 4.99 (s, 2H), 5.16 (s, 2H) 5 5.98 (dd 5 IH), 6.08 (d, IH), 7.20-7.42 (m, 8H)
  • Example 65 l-(2,4-dichloro-benzyl)-4-(4-methyl-benzyloxy)-lH-pyridin-2-one 1 H NMR (CDCl 3 , 300 MHz) ⁇ 2.37 (s, 3H) 5 4.95 (s, 2H), 5.15 (s, 2H) 5 5.98 (dd, IH), 6.03 (d, IH) 5 7.18-7.30 (m, 8H)
  • Example 66 l-(2-nitro-benzyl)-4-pentyloxy-lH-pyridin-2-one 1 H NMR (CDCl 3 , 300 MHz) ⁇ 0.93 (t, 3H), 1.34-1.43 (m, 4H) 5 1.73-1.82 (m, 2H), 3.93 (t, 2H), 5.46 (s, 2H) 5 5.93 (d, IH), 5.98 (dd, IH), 7.10 (d, IH), 7.17 (d, IH) 5 7.44 (t, IH), 7.56 (t, IH), 8.10 (d, IH)
  • Example 67 l-(2-amino-benzyl)-4-pentyloxy-lH-pyridin-2-one 1 H NMR (CDCl 3 , 300 MHz) ⁇ 0.91 (t, 3H) 5 1.30-1.39 (m, 4H), 1.69-1.76 (m, 2H) 5 3.89 (t, 2H), 4.75 (br s, 2H) 5 5.00 (s, 2H) 5 5.89-5.93 (m, 2H) 5 6.62-6.70 (m, 2H), 7.09-7.23 (m, 3H)
  • Example 68 N-[2-(2-oxo-4-pentyloxy-2H-pyridin-l-ylmethyl)-phenyl]-acetamide 1 H NMR (CDCl 3 , 300 MHz) ⁇ 0.92 (t, 3H) 5 1.26-1.38 (m, 4H) 5 1.74-1.78 (m, 2H), 2.29 (s, 3H), 3.91 (t, 2H), 5.01 (s, 2H), 5.94 (d, IH), 6.01 (dd, IH) 5 7.08 (t, IH), 7.31-7.38 (m, 3H), 8.20 (d, IH), 10.56 (br s, IH)
  • Example 70 N-[4-(4-benzyloxy-2-oxo-2H-pyridin-l -ylmethyl)-phenyl]acetamide 1 H NMR (CDCl 3 , 300 MHz) ⁇ 2.18 (s, 3H) 5 4.99 (s, 2H), 5.04 (s, 2H), 5.98 (dd, IH) 5 6.02 (d, IH) 5 7.14-7.46 (m, 10H) 5 7.82 (br s, IH)
  • Example 71 l-(2,4-dichloro-benzyl)-4-(naphthalen-2-ylmethoxy)-lH-pyridin-2-one 1 H NMR (CDCl 3 , 300 MHz) ⁇ 5.15 (s, 2H), 5.16 (s, 2H) 5 5.99-6.09 (m, 2H), 7.18-7.55 (m, 7H) 5 7.83-7.90 (m, 4H)
  • Example 72 1 -naphthalen ⁇ -ylmethyM-pentyloxy-lH-pyridin ⁇ -one 1 B NMR (CDCl 3 , 300 MHz) ⁇ 0.92 (t, 3H) 5 1.35-1.43 (m, 4H) 5 1.73-1.76 (m, 2H), 3.91 (t, 2H) 5 5.24 (s, 2H), 5.84-5.96 (m, 2H) 5 7.13 (d, IH), 7.26-7.49 (m, 3H), 7.70 (s, IH), 7.79-7.83 (m, 3H)
  • Example 73 4-benzyloxy- 1 -(6-chloro-benzo[ 1 ,3]dioxol-5-ylmethyl)- 1 H-pyridin-2-one 1 H NMR (CDCl 3 , 300 MHz) ⁇ 4.99 (s, 2H), 5.10 (s, 2H), 5.94-6.03 (m, 4H), 6.84 (d, 2H) 5 7.20 (d, IH), 7.33-7.39 (m, 5H)
  • Example 76 4-(3-methyl-butoxy)-l-(2-nitro-benzyl)-lH-pyridin-2-one 1 H NMR (CDCl 3 , 300 MHz) ⁇ 0.93 (d, 6H), 1.65 (q, 2H), 1.69-1.78 (m, IH), 3.95 (t, 2H), 5.45 (s, 2H), 5.93-5.96 (m, 2H), 7.11 (d, IH), 7.14 (d, IH), 7.44 (t, IH), 7.53 (t, IH), 8.08 (d, IH)
  • Example 77 l-(2,4-dichloro-beiizyl)-4-pentylamino-l H-pyridin-2-one 1 H NMR (CDCl 3 , 300 MHz) ⁇ 0.88 (t, 3H), 1.24-1.34 (m, 4H), 1.57-1.84 (m, 2H), 3.19 (br s, IH), 3.47 (q, 2H), 5.03 (s, 2H) 5 5.56 (d, IH), 7.15-7.38 (m, 4H)
  • Example 81 4-(5-benzyloxy-pentyloxy)-l-(6-chloro-benzo[l,3]dioxol-5-ylmethyl) - lH-pyridin-2-one
  • Example 82 l-(2-chloro-benzyl)-4-(3-methyl-butoxy) -lH-pyridin-2-one 1 H NMR (CDCl 3 , 300 MHz) ⁇ 0.93 (d, 6H) 5 1.60-1.82 (m, 3H), 3.94 (t, 2H) 5 5.17 (s, 2H), 5.86-5.94 (m, 2H) 5 7.12-7.40 (m, 5H)
  • Example 84 l-(2 5 4-dichloro-5-fluoro-benzyl)-4-(3-methyl-butoxy) -lH-pyridin-2-one 1 H NMR (CDCl 3 , 300 MHz) ⁇ 0.92 (d 5 6H), 1.64 (q, 2H) 5 1.71-1.82 (m, IH) 5 3.93 (t, 2H), 5.08 (s, 2H), 5.90-5.92 (m, 2H) 5 7.00 (d, IH) 5 7.12-7.15 (m, IH), 7.42 (d, IH)
  • Example 85 l-benzyl-4-(3-methyl-butoxy)-lH-pyridin-2-one 1 U NMR (CDCl 3 , 300 MHz) ⁇ 0.95 (d, 6H), 1.59-1.78 (m, 3H), 3.93 (t, 2H) 9 5.08 (s, 2H), 5.83-5.93 (m, 2H), 7.07-7.36 (m, 6H)
  • Example 86 l-(4-chloro-benzyl)-4-(3-methyl-butoxy)-lH-pyridin-2-one 1 H NMR (CDCl 3 , 300 MHz) ⁇ 0.92 (d, 6H), 1.62 (q, 2H), 1.71-1.80 (m, IH), 3.91 (t, 2H), 5.01 (s, 2H), 5.85 (dd, IH), 5.89 (d, IH), 7.06 (d, IH), 7.19 (d, 2H), 7.27 (d, 2H)
  • Example 87 1 -(2,4-dichloro-benzyl)-4-pentyloxy-lH-pyrimidin-2-one 1 H NMR (CDCl 3 , 300 MHz) ⁇ 0.88 (t, 3H), 1.32-1.36 (m, 4H), 1.61-1.73 (m, 2H), 4.33 (t, 2H), 5.07 (s, 2H), 5.83 (d, IH), 7.22 (d, IH), 7.35-7.45 (m, 3H)
  • Example 88 l-(2,4-dichloro-benzyl)-4-(4-methyl-pentyloxy)-lH-pyrimidin-2-one 1 H NMR (CDCl 3 , 300 MHz) ⁇ 0.89 (d, 6H), 1.20-1.76 (m, 5H), 4.34 (t, 2H), 5.09 (s, 2H), 5.85 (d, IH), 7.22 (d, IH), 126-1 Al (m, 3H)
  • Example 90 4-(butyl-methyl-amino)- 1 -(2,4-dichloro-benzyl)- 1 H-pyrimidin-2-one 1 H NMR (CDCl 3 , 300 MHz) ⁇ 0.90 (t, 3H), 1.19-1.56 (m, 4H), 2.81-3.11 (m, 3H), 3.22- 3.27 (m, IH), 3.59-3.62 (m, IH), 4.98 (s, 2H), 5.72-5.75 (m, IH), 7.12-7.31 (m, 4H)
  • Example 91 1 -(2,4-dichloro-benzyl)-4-(2-diethylamino-ethoxy)- 1 H-pyrimidin-2-one 1 R NMR (CDCl 3 , 300 MHz) ⁇ 1.04 (t, 6H), 2.62 (q, 4H), 2.84 (t, 2H), 4.46 (t, 2H), 5.09 (s, 2H), 5.90 (d, IH), 7.21-7.54 (m, 4H)
  • Example 92 4-butoxy-l-(2,4-dichloro ⁇ benzyl)-lH-pyrimidin-2-one 1 H NMR (CDCl 3 , 300 MHz) ⁇ 0.95 (t, 3H), 1.39-1.46 (m, 2H), 1.69-1.74 (m, 2H) 5 4.37 (t, 2H), 5.10 (s, 2H), 5.87 (d, IH), 7.23-7.48 (m, 4H)
  • Example 95 1 -(2-methyl-3-nitro-benzyl)-4-pentyloxy- lH-pyridin-2-one 1 H NMR (CDCl 3 , 300 MHz) ⁇ 0.92 (t, 3H) 5 1.33-1.43 (m, 4H) 5 1.75 (m, 2H) 5 2.40 (s, 3H), 3.92 (t, 2H) 5 5.13 (s, 2H) 5 5.92-5.95 (m, 2H), 6.98 (dd, IH), 7.16 (d, IH) 5 7.28 (t, IH) 5 7.69 (d, IH)
  • Example 96 1 -(3-amino-2-methyl-benzyl)-4-pentyloxy-lH-pyridin-2-one 1 H NMR (CDCl 3 , 300 MHz) ⁇ 0.92 (t, 3H), 1.33-1.43 (m, 4H), 1.71-1.80 (m, 2H) 5 2.01 (s, 3H) 5 3.72 (s 5 2H), 3.91 (t, 2H), 5.05 (s, 2H) 5 5.81 (dd, IH), 5.92 (d, IH), 6.56 (d, IH) 5 6.69 (d, IH), 6.90 (d, IH), 7.01 (t, IH)
  • Example 97 1 -(4-methoxy-3,5-dimethyl-pyridin-2-ylmethyl)-4-pentyloxy-lH-pyridin- 2-one
  • Example 98 l-(6-chloro-benzo[l,3]dioxol-5-ylmethyl)-4-(5-hydroxy-pentyloxy) -IH- pyridin-2-one 1 H NMR (CD 3 OD, 300 MHz) ⁇ 1.48-1.58 (m, 4H), 1.75-1.80 (m, 2H) 5 3.54 (t, 2H) 5 3.97 (t, 2H), 5.06 (s, 2H), 5.89 (d, IH), 5.94 (s, 2H), 6.07 (dd, IH), 6.61 (s, IH), 6.90 (s, IH), 7.43 (d, IH)
  • Example 99 1 -(2-methoxy-5 -nitro-benzyl)-4-pentyloxy- 1 H-pyridin-2-one 1 H NMR (CDCl 3 , 300 MHz) ⁇ 0.92 (t, 3H), 1.36-1.44 (m, 4H), 1.74-1.80 (m, 2H), 3.91 (t, 2H), 3.97 (S, 3H), 5.07 (s, 2H), 5.90-5.95 (m, 2H), 7.17 (d, IH), 7.21 (d, IH), 8.03 (d, IH), 8.19 (dd, IH)
  • Example 100 l-(5-amino-2-methoxy-benzyl)-4-pentyloxy-l H-pyridin-2-one 1 H NMR (CDCl 3 , 300 MHz) ⁇ 0.92 (t, 3H), 1.24-1.39 (m, 4H), 1.73-1.78 (m, 2H), 3.79 (s, 2H), 3.90 (t, 2H), 5.02 (s, 2H), 5.83 (dd, IH), 5.89 (d, IH), 6.59-6.74 (m, 3H), 7.23- 7.27 (m, 3H)
  • Example 101 l-(2-ethyl-benzyl)-4-pentyloxy-l H-pyridin-2-one 1 H NMR (CDCl 3 , 300 MHz) ⁇ 0.93 (t, 3H) 5 1.18 (t, 3H) 5 1.34-1.43 (m, 4H) 5 1.73-1.79 (m, 2H) 5 2.63 (q, 2H) 5 3.93 (t, 2H) 5 5.12 (s, 2H) 5 5.84 (dd, IH) 5 5.94 (d, IH) 5 6.92 (d, IH) 5 7.05 (d, IH) 5 7.16-7.32 (m, 3H)
  • Example 104 1 -(4-methoxy-2,3 -dimethyl-benzyl)-4-pentyloxy- 1 H-pyridin-2-one 1 H NMR (CDCl 35 300 MHz) ⁇ 0.93 (t, 3H), 1.31-1.42 (m, 4H), 1.72-1.81 (m, 2H) 5 2,12 (s, 3H), 2.16 (s, 3H), 3.82 (s, 3H), 3.91 (t, 2H), 5.04 (s, 2H) 5 5.80 (dd, IH) 5 5.93 (d, IH), 6.71 (d, IH), 6.85 (d, IH) 5 6.97 (d, IH)
  • Example 105 l-(2-methyl-pyridin-3-ylmethyl)-4-pentyloxy-l H-pyridin-2-one 1 H NMR (CDCl 3 , 300 MHz) ⁇ 0.93 (t, 3H), 1.32-1.47 (m, 4H), 1.73-1.83 (m, 2H), 2.56 (s, 3H), 3.93 (t, 2H) 5 5.09 (s, 2H), 5.91-5.94 (m, 2H) 5 7.00 (d, IH), 7.08-7.13 (m, IH), 7.26-7.28 (m, IH), 8.43 (d, IH)
  • Example 107 1 -(2,4-dichloro-benzyl)-4-(3-dimethylamino-propoxy)-lH-pyridin-2-one 1 H NMR (CDCl 3 , 300 MHz) ⁇ 1.87-1.97 (m, 2H), 2.25 (s, 6H), 2.40 (t, 2H), 4.42 (t, 2H), 5.10 (s, 2H), 5.87 (d, IH), 7.23-7.49 (m, 4H)
  • Example 108 l-(2,4-dichloro-benzyl)-4-(4-dimethylamino-butoxy)-lH-pyridin-2-one 1 H NMR (CDCl 3 , 300 MHz) ⁇ 1.52-1.81 (m, 4H) 5 2.22 (s, 6H), 2.29 (t, 2H), 4.38 (t, 2H), 5.10 (s, 2H), 5.86 (d, IH), 7.23-7.48 (m, 4H)
  • Example 109 l-(2 5 4-dichloro-benzyl)-4-(6-dimethylamino-hexyloxy)-lH-pyrimidin-2- one
  • Example 110 1 -(2,4-dimethyl-benzyl)-4-pentyloxy- 1 H-pyridin-2-one 1 H NMR (CDCl 3 , 300 MHz) ⁇ 0.92 (t, 3H) 5 1.33-1.42 (m, 4H) 5 1.71-1.76 (m, 2H) 5 2.22 (S 5 3H) 5 2.31 (s 5 3H) 5 3.91 (t, 2H), 5.03 (s, 2H) 5 5.83 (dd 5 IH) 5 5.92 (d, IH), 6.89-7.20 (m, 4H)
  • Example 111 1 -(2-chloro-5-trifluoromethyl-benzyl)-4-pentyloxy- 1 H-pyridin-2-one 1 H NMR (CDCl 3 , 300 MHz) ⁇ 0.93 (t, 3H) 5 1.34-1.46 (m, 4H) 5 1.74-1.83 (m, 2H) 5 3.93 (t, 2H) 5 5.21 (s, 2H) 5 5.94-6.15 (m, 2H) 5 7.17 (d, IH) 5 7.43-7.54 (m, 3H)
  • Example 112 l-(2-hydroxy-benzyl)-4-pentyloxy-lH-pyridin-2-one 1 H NMR (CDCl 35 300 MHz) ⁇ 0.91 (t, 3H) 5 1.29-1.43 (m, 4H), 1.70-1.79 (m, 2H) 5 3.90 (t, 2H) 5 4.99 (s 5 2H) 5 5.97 (d, IH), 6.04 (dd, IH) 5 6.83 (t, IH) 5 6.95 (dd, IH) 5 7.19-7.24 (m, 2H) 5 7.38 (d, IH) 5 10.45 (br s, IH)
  • Example 113 4-(3-cyclo-propoxy)-l -(2,4-dichloro-benzyl)-lH-pyrimidin-2-one 1 H NMR (CDCl 3 , 300 MHz) ⁇ 1.27-1.25 (m, 2H), 1.51-1.82 (m, 9H) 5 4.37 (t, 2H) 5 5.10 (S 5 2H) 5 5.85 (d, IH), 7.22 (d, IH) 5 7.38-7.47 (m, 3H)
  • Example 114 l-(2,4-dichloro-benzyl)-4-(3-methyl-pentyloxy)-lH-pyrimidin-2-one 1 H NMR (CDCl 3 , 300 MHz) ⁇ 0.85-2.03 (m, HH) 5 4.39 (t, 2H) 5 5.10 (s, 2H) 5 5.85 (d, IH), 122-1 Al (m, 4H)
  • Example 115 1 -(2,4-dichloro-benzyl)-4-hex-4-enyloxy- 1 H-pyrimidin-2-one 1 H NMR (CDCl 3 , 300 MHz) ⁇ 1.25-2.10 (m, 7H) 5 4.35 (t, 2H) 5 5.10 (s, 2H) 5 5.40-5.46 (m, 2H) 5 5.86 (d, IH) 5 7.23-7 '.47 (m, 4H)
  • Example 116 4-(2-cyclopropyl-ethoxy)-l-(2,4-dichloro-benzyl)-l H-pyrimidin-2-one 1 H NMR (CDCl 35 300 MHz) ⁇ 0.42-0.96 (m, 3H) 5 1.25-1.66 (m, 4H), 4.43 (t, 2H) 5 5.10 (s, 2H), 5.87 (d 5 IH) 5 1.22-1 Al (m, 4H)
  • Example 117 1 -(2,4-dichloro-benzyl)-4-(3-methyl-pentyloxy)- 1 H-pyridin-2-one 1 H NMR (CDCl 3 , 300 MHz) ⁇ 0.85-0.91 (m, 6H), 1.17-1.24 (m, IH), 1.33-1.39 (m, IH), 1.51-1.58 (m, 2H), 1.78-1.80 (m, IH), 3.93 (t, 2H), 5.12 (s, 2H), 5.88-5.92 (m,
  • Example 118 1 -(2,4-dichloro-benzyl)-4-(5-morpholin-4-yl-pentyloxy)-lH-pyridin-2- one
  • Example 119 1 -(2-chloro-5-methoxy-benzyl)-4-pentyloxy-lH-pyridin-2-one 1 H NMR (CDCl 3 , 300 MHz) ⁇ 0.93 (t, 3H), 1.33-1.43 (m, 4H), 1.72-1.79 (m, 2H), 3.74 (s, 3H), 3.91 (t, 2H), 5.15 (s, 2H), 5.88-5.93 (m, 2H), 6.76-6.79 (m, 2H), 7.15 (d, IH), 7.27 (d, IH)
  • Example 120 l-(2-chloro-5-ethoxy-benzyl)-4-pentyloxy-lH-pyridin-2-one 1 H NMR (CDCl 3 , 300 MHz) ⁇ 0.93 (t, 3H), 1.25-1.40 (m, 7H), 1.72-1.81 (m, 2H), 3.89- 3.99 (m, 4H), 5.15 (s, 2H), 5.89-5.92 (m, 2H), 6.75-6.77 (m, 2H), 7.15 (d, IH), 7.26 (d, IH)
  • Example 122 1 - [2-chloro-5-(2-hydroxy-ethoxy)-benzyl] -4-pentyloxy- 1 H-pyridin-2- one 1 H NMR (CDCl 3 , 300 MHz) ⁇ 0.90 (t, 3H) 5 1.25-1.43 (m, 4H), 1.72-1.79 (m, 2H), 2.13 (t, IH), 3.91 (t, 4H), 4.01 (t, 2H), 5.15 (s, 2H), 5.86-5.92 (m, 2H) 3 6.76-6.83 (m, 2H), 7.18 (d, IH), 7.28 (d, IH)
  • Example 124 l-[5-(2-amino-ethoxy)-2-chloro-benzyl]-4-pentyloxy-lH-pyridin-2-one 1 H NMR (CDCl 3 , 300 MHz) ⁇ 0.93 (t, 3H), 1.41-1.44 (m, 4H), 1.78-1.82 (m, 2H), 3.93 (t, 2H), 4.01 (t, 4H) 5 5.17 (s, 2H) 5 5.96 (d, IH) 5 7.13 (dd, IH) 5 6.60 (s, IH), 6.90 (d 5 IH), 7.34 (d, IH), 7.49 (d, IH)
  • Example 127 l-(3-dimethylamino-2-methyl-benzyl)-4-phenyloxy-lH- ⁇ yridin-2-one 1 H NMR (CDCl 3 , 300 MHz) ⁇ 0.93 (t, 3H), 1.36-1.43 (m, 4H), 1.75-1.79 (m, 2H), 2.22 (S 5 3H), 2.69 (s, 6H), 3.92 (t, 2H) 5 5.07 (s, 2H), 5.86 (dd, IH), 5.95 (d, IH) 5 6.72 (d, IH), 6.93 (d, IH), 7.05 (d, IH) 5 7.15 (t, IH)
  • Example 128 l-(3-ethylamino-2-methyl-benzyl)-4-pentyloxy-lH-pyridin-2-one 1 H NMR (CDCl 3 , 300 MHz) ⁇ 0.92 (t, 3H), 1.31 (t, 3H), 1.33-1.42 (m, 4H) 5 1.71-1.78 (m, 2H) 5 1.97 (s, 3H), 3.19 (q, 2H), 3.48 (br s, IH) 5 3.90 (t, 2H) 5 5.06 (s, 2H), 5.79 (dd, IH) 5 5.93 (d, IH), 6.56 (d, IH), 6.65 (d, IH) 5 6.89 (d, IH), 7.13 (t, IH)
  • Example 129 l-(3-diethylamino-2-methyl-benzyl)-4-pentyloxy-lH-pyridin-2-one 1 H NMR (CDCl 3 , 300 MHz) ⁇ 0.96 (t, 9H) 5 1.34-1.44 (m, 4H), 1.75-1.80 (m, 2H), 2.21 (s, 3H), 2.95 (q, 4H), 3.92 (t, 2H), 5.08 (s, 2H), 5.87-5.95 (m, 2H), 6.73 (d, IH) 5 6.95- 7.16 (m, 3H)
  • Example 131 l-(3-dipropylamino-2-methyl-benzyl)-4-pentyloxy-lH-pyridin-2-one 1 H NMR (CDCl 35 300 MHz) ⁇ 0.83 (t, 6H), 0.93 (t, 3H) 5 1.34-1.47 (m, 8H) 5 1.75-1.80 (m 5 2H) 5 2.22 (s, 3H), 2.82-2.87 (m, 4H) 5 3.93 (t, 2H) 5 5.07 (s, 2H) 5 5.87 (dd 5 IH) 5 5.96 (d, IH) 5 6.69 (d, IH) 5 6.94 (d, IH), 7.07-7.15 (m, 2H)
  • Example 132 l-[3-(2-hydroxy-ethylamino)-2-methyl-benzyl]-4-pentyloxy-lH-pyridin- 2-one 1 H NMR (CDCl 3 , 300 MHz) ⁇ 0.92 (t, 3H) 5 1.32-1.41 (m, 4H), 1.71-1.78 (m, 2H), 1.83 (br s, IH), 2.01 (s, 3H), 3.34 (t, 2H), 3.90 (t, 4H) 5 4.02 (br S 5 IH), 5.06 (s, 2H) 5 5.81 (dd, IH), 5.92 (d, IH), 6.57 (d, IH) 5 6.67 (d, IH), 6.89 (d, IH), 7.12 (t, IH)
  • Example 133 l-(2-chloro-5-methoxy-4-nitro-benzyl)-4-pentyloxy-lH-pyridin-2-one 1 H NMR (CDCl 3 , 300 MHz) ⁇ 0.94 (t, 3H) 5 1.37-1.44 (m, 4H) 5 1.76-1.81 (m, 2H), 3.91 (s, 3H), 3.93 (t, 2H) 5 5.20 (s, 2H) 5 5.93 (d, IH), 5.97 (dd, IH), 7.18 (s, IH) 5 7.26 (d, IH) 5 7.93 (s 5 IH)
  • Example 134 l-(4-amino-2-chloro-5-methoxy-benzyl)-4-pentyloxy-lH-pyridin-2-one 1 H NMR (CDCl 35 300 MHz) ⁇ 0.92 (t, 3H) 5 1.32-1.42 (m, 4H) 5 1.71-1.78 (m, 2H), 3.81 (t, 3H), 3.87-3.93 (m, 4H) 5 5.09 (s, 2H) 5 5.85 (dd, IH) 5 5.90 (d, IH), 6.69 (s, IH), 6.91 (s 5 IH), 7.21 (d, IH)
  • Example 136 1 -(2-chloro-5-methoxy-4-methylamino-benzyl)-4-pentyloxy- 1 H-pyridin- 2-one
  • Example 137 1 -(2-chloro-4-dimethylamino-5-methoxy-benzyl)-4-pentyloxy- 1 H- pyridin-2-one
  • Example 138 1 -(2-chloro-4-ethylamino-5-methoxy-benzyl)-4-pentyloxy- 1 H-pyridin- 2-one 1 H NMR (CDCl 3 , 300 MHz) ⁇ 0.92 (t, 3H), 1.28 (t, 3H), 1.36-1.41 (m, 4H), 1.71-1.77 (m, 2H), 3.13 (t, 2H), 3.80 (s, 3H), 3.89 (t, 2H), 4.23 (br s, IH), 5.10 (s, 2H), 5.84 (dd, IH), 5.90 (d, IH), 6.52 (s, IH), 6.87 (s, IH), 7.22 (d, IH)
  • Example 140 1 -[2-chloro-4-(2-hydroxy-ethylamino)-5-methoxy-benzyl]-4-pentyloxy- lH-pyridin-2-one
  • Example 141 1 -(4-amino-6-chloro-3-methoxy-2-nitro-benzyl)-4-pentyloxy- 1 H- pyridin-2-one
  • Example 142 l-(2,4-diamino-6-chloro-3-methoxy-benzyl)-4-pentyloxy-lH-pyridin-2- one
  • Example 143 1 -(2,5-dichloro-6-methoxy-pyrimidin-4-ylmethyl)-4-pentyloxy-lH- pyridin-2-one H NMR (CDCl 3 , 300 MHz) ⁇ 0.93 (t, 3H), 1.34-1.45 (m, 4H), 1.73-1.82 (m, 2H), 3.92 (t, 2H), 4.08 (s. 3H), 5.14 (s, 2H), 5.86 (d, IH), 5.96 (dd, IH), 7.19 (d, IH)
  • Example 144 l-(2,4-dichloro-benzenesulfonyl)-4-pentyloxy-lH-pyridin-2-one 1 H NMR (CDCl 3 , 300 MHz) ⁇ 0.90 (t, 3H), 1.32-1.40 (m, 4H), 1.72-1.79 (m, 2H), 3.89 (t, 2H), 5.60 (d, IH), 6.05 (dd, IH), 7.47-7.51 (m, 2H) 5 7.95 (d, IH), 8.35 (d, IH)
  • Example 145 1 -(4-methanesulfonyl-benzyl)-4-pentyloxy-lH-pyridin-2-one 1 H NMR (CDCl 3 , 300 MHz) ⁇ 0.94 (t, 3H), 1.34-1.45 (m, 4H), 1.74-1.83 (m, 2H), 3.04 (s, 3H), 3.94 (t, 2H) 5 5.22 (s, 2H) 5 5.93 (d, IH), 5.99 (dd, IH), 7.20 (d, IH), 7.32 (d, IH), 7.76 (dd, IH), 7.97 (d, IH)
  • Example 146 1 -(4-amino-2-chloro-5-hydroxy-benzyl)-4-pentyloxy- 1 H-pyridin-2-one 1 H NMR (CDCl 3 , 300 MHz) ⁇ 0.91 (t, 3H), 1.29-1.41 (m, 4H), 1.66-1.75 (m, 2H), 3.78 (t, 2H), 5.13 (s, 2H), 5.85 (d, IH), 5.94 (dd, IH), 6.68 (s, IH), 7.18 (s, IH), 7.44 (d, IH)
  • Example 147 4-(4-bromo-butoxy)-l-(2,4-dichloro-benzyl) -1 H-pyridin-2-one 1 H NMR (CDCl 3 , 300 MHz) ⁇ 1.88-2.08 (m, 4H), 3.46 (t, 2H), 3.95 (t, 2H), 5.13 (s, 2H), 5.88-5.92 (m, 2H), 7.16-7.24 (m, 3H), 7.40 (s, IH)
  • Example 148 4-[ 1 -(2,4-dichloro-benzyl)-2-oxo- 1 ,2-dihydro-pyridin-4-yloxy] - butylammonium
  • Example 150 1 -(2-amino-5-chloro-6-methoxy-pyrimidin-4-ylmethyl)-4-pentyloxy-lH- pyridin-2-one
  • Example 151 1 -(6-amino-2,5-dichloro-pyrimidin-4-ylmethyl)-4-pentyloxy- 1 H- pyridin-2-one
  • Example 154 l-(2-chloro-4-isopropoxy-benzyl)-4-pentyloxy-lH-pyridin-2-one 1 H NMR (CDCl 35 300 MHz) ⁇ 0.92 (t, 3H) 5 1.31 (d, 6H), 1.35-1.45 (m, 4H) 5 1.73-1.80 (m, 2H) 5 3.90 (t, 2H) 5 4.46-4.54 (m. IH), 5.11 (s, 2H) 3 5.85-5.91 (m, 2H), 6.74 (dd, IH), 6.91 (d, IH), 7.16 (d IH), 7.23 (d, IH)
  • Example 155 2-[3-(2-oxo-4-pentyloxy-2H-pyridin-l-yl)-propyl]-isoindole-l,3-dione 1 H NMR (CDCl 3 , 300 MHz) ⁇ 0.93 (t, 3H) 5 1.20-1.33 (m, 4H) 5 1.71-1.80 (m, 2H) 5 2.09- 2.18 (m, 2H), 3.75 (t, 2H) 5 3.87-3.94 (m, 4H) 5 5.86 (d, IH), 5.91 (dd, IH), 7.27 (s, IH), 7.72-7.76 (m, 2H), 7.83-7.87 (m, 2H) .
  • Example 156 l-(3-amino-propyl)-4-pentyloxy-lH-pyridin-2-one 1 H NMR (CDCl 3 , 300 MHz) ⁇ 0.93 (t, 3H), 1.36-1.44 (m, 4H), 1.75-1.80 (m, 2H) 5 2.26- 2.30 (m, 2H) 5 3.00 (t, 2H) 5 3.91 (t, 2H), 4.10 (t, 2H), 5.90 (d, IH), 6.02 (d, IH) 5 7.25 (d, IH)
  • Example 157 N-[3-(2-oxo-4-pentyloxy-2H-pyridin- 1 -yl)-propyl]-acetamide 1 H NMR (CDCl 3 , 300 MHz) ⁇ 0.93 (t, 3H), 1.34-1.44 (m, 4H), 1.73-1.89 (m, 4H) 5 2.01 (s, 3H), 3.15-3.21 (m, 2H), 3.92 (t, 2H) 5 3.98 (t, 2H), 5.89 (d, IH), 5.98 (dd, IH), 7.08 (br s, IH) 5 7.14 (d, IH)
  • Example 158 l-(3-dimethylamino-propyl)-4-pentyloxy-lH-pyridin-2-one 1 H NMR (CDCl 3 , 300 MHz) ⁇ 0.93 (t, 3H), 1.37-1.42 (m, 4H), 1.72-1.78 (m, 4H) 5 2.31-
  • Example 160 l-(2,4-dichloro-benzyl)-6-methyl-3-pentyl-4-pentyloxy-lH-pyridin-2- one
  • Example 165 l-(7-nitro-benzo[l,3]dioxol-5-ylmethyl)-4-pentyIoxy-lH-pyridin-2-one 1 H NMR (CDCl 3 , 300 MHz) ⁇ 0.95 (t, 3H), 1.32-1.42 (m, 4H), 1.75-1.82 (m, 2H), 3.95 (t, 2H), 5.42 (s, 2H), 5.94-6.00 (m, 2H), 6.09 (s, 2H) 5 6.55 (s, IH), 7.18 (d, IH), 7.63 (s, IH)
  • Example 166 1 -(2-chloro-3 -nitro-benzyl)-4-pentyloxy- 1 H-pyridin-2-one 1 H NMR (CDCl 3 , 300 MHz) ⁇ 0.97 (t, 3H), 1.27-1.53 (m, 4H), 1.77-1.82 (m, 2H) 5 3.95 (t, 2H), 5.25 (s 5 2H) 5 5.96-6.00 (m, 2H) 5 7.22 (d, IH), 7.35-7.44 (m, 2H), 7.73 (d, IH)
  • Example 167 1 -(3 -amino-2-chloro-benzyl)-4-pentyloxy-l H-pyridin-2-one 1 U NMR (CDCl 3 , 300 MHz) ⁇ 0.91 (t, 3H) 5 1.37-1.43 (m, 4H) 5 1.72-1.76 (m, 2H), 3.89 (t, 2H) 5 4.13 (br s), 5.12 (s, 2H) 5 5.86-5.92 (m, 2H) 5 6.47 (d, IH) 5 6.70 (d, IH) 5 6.96- 7.07 (m, 2H)
  • Example 168 N-[2-chloro-3-(2-oxo-4-pentyloxy-2H-pyridin-l-ylmethyl)-phenyl]- acetamide
  • Example 169 N-[2 5 chloro-3-(2-oxo-4-pentyloxy-2H-pyridin-l -ylmethyl)-phenyl]- methanesulfonamide 1 H NMR (CDCl 35 300 MHz) ⁇ 0.94 (t, 3H), 1.37-1.43 (m, 4H), 1.75-1.81 (m, 2H), 3.03 (s, 3H) 5 3.94 (t, 2H), 5.18 (s, 2H), 5.94-5.97 (m, 2H), 6.90 (d, IH), 7.00 (br s, IH), 7.12 (d, IH) 5 7.28 (d, IH), 7.60 (d, IH)
  • Example 171 l-[2-chloro-3-(2-hydroxy-ethylamino)-benzyl]-4-pentyloxy-lH-pyridin- 2-one
  • Example 174 l-(3-amino-2,6-dichloro-benzyl)-4-pentyloxy-lH-pyridin-2-one 1 H NMR (CDCl 3 , 300 MHz) ⁇ 0.92 (t, 3H) 3 1.25-1.44 (m, 4H) 5 1.70-1.80 (m, 2H), 3.90 (t, 2H) 5 4.19 (s 5 2H) 5 5.33 (s, 2H), 5.79 (dd, IH) 5 5.92 (d, IH), 6.74 (dd, 2H), 7.18 (d, IH)
  • Example 175 1 -(3-benzyloxy-2-chloro-4-methoxy-benzyl)-4-pentyloxy- lH-pyridin-2- one
  • Example 176 l-(2-chloro-3,4-dimethoxy-benzyl)-4-pentyloxy-lH-pyridin-2-one
  • Example 178 l-[2-chloro-4-methoxy-3-(2-methoxy-ethoxy)-benzyl]-4-pentyloxy-lH- pyridin-2-one
  • Example 179 l-[2-chloro-4-methoxy-3-(2-pyrrolidin-l-yl-ethoxy)-benzyl]-4- pentyloxy- 1 H-pyridin-2-one
  • Example 180 1 -[2-chloro-3-(2-dimethylammo-ethoxy)-4-methoxy-benzyl]-4- pentyloxy- 1 H-pyridin-2-one
  • Example 181 2- ⁇ 3-[2-chloro-6-methoxy-3-(2-oxo-4-pentyloxy-2H-pyridin-l- ylmethyl)-phenoxyl] -propyl ⁇ -isoindole- 1 ,3 -dione 1 K NMR (CDCl 3 , 300 MHz) ⁇ 0.92 (t, 3H), 1.28-1.38 (m, 4H), 1.73-1.77 (m, 2H), 3.59 (s, 3H), 3.89 (t, 2H) 5 4.12 (t, 2H) 5 4.26 (t, 2H), 5.03 (s, 2H) 5 5.85-5.91 (m, 2H), 6.69 (d, IH) 5 6.95 (d, IH), 7.08 (d, IH) 5 7.74 (d, 2H), 7.87 (d, 2H)
  • Example 182 l-[3-(2-dimethylamino-ethoxy)-2-methyl-benzyl]-4-pentyloxy-lH- pyridin-2-one
  • Example 184 1 -[2 5 6-dichloro-3-(2-hydroxy-ethylamino)-benzyl]-4-pentyloxy- 1 H- pyridin-2-one
  • Example 185 l-[2 5 6-dichloro-3-(2-dimethylamino-ethylamino)-benzyl]-4-pentyloxy- lH-pyridin-2-one 1 H NMR (CD 3 OD 5 300 MHz) ⁇ 0.93 (t, 3H), 1.38-1.46 (m, 4H), 1.75-1.80 (m, 2H), 2.55 (s, 6H), 2.91 (t, 2H), 3.46 (t, 2H) 5 3.99 (t, 2H), 5.32 (s, 2H) 5 5.96 (d, IH) 5 6.02 (dd, IH), 6.88 (d, IH) 5 6.93 (d, IH) 5 7.35 (d, IH)
  • Example 188 l-[3-(3-amino-propylamino)-2,6-dichloro-benzyl]-4-pentyloxy-lH- pyridin-2-one
  • Example 190 l-(2-chloro-3-dimethylaminomethyl-4-fluoro-benzyl)-4-pentyloxy-lH- pyridin-2-one
  • Example 191 l-(2,6-dichloro-3-methylamino-benzyl)-4-pentyloxy-lH-pyridin-2-one 1 H NMR (CDCl 3 , 300 MHz) ⁇ 0.92 (t, 3H) 5 1.32-1.42 (m, 4H) 5 1.75-1.79 (m, 2H), 2.91 (d, 3H) 5 3.90 (t, 2H) 5 4.49 (q, IH) 5 5.33 (s, 2H) 5 5.78 (dd, IH) 5 5.92 (d, IH) 5 6.63 (d, IH) 5 6.70 (d, IH) 5 7.28 (d, IH)
  • Example 192 l-(2,6-dichloro-3-dimethylamino-benzyl)-4-pentyloxy-lH-pyridin-2-one 1 H NMR (CDCl 3 , 300 MHz) ⁇ 0.92 (t, 3H) 5 1.34-1.41 (m, 4H) 5 1.72-1.78 (m, 2H) 5 2.80 (s, 6H) 5 3.90 (t, 2H), 5.38 (s, 2H) 5 5.79 (dd, IH) 5 5.93 (d, IH) 5 6.69 (d, IH), 7.08 (d, IH) 5 7.33 (d, IH)
  • Example 195 1 -( ⁇ -chloro-benzotl ⁇ Jdioxol-S-ylmethyO ⁇ -C ⁇ -chloro-pyridin-S- ylmethoxy) -lH-pyridin-2-one
  • Example 196 l-(6-chloro-benzo[l ,3]dioxol-5-ylmethyl)-4-(4-methoxy-3,5- dimethylpyridin-2-ylmethoxy)-lH-pyridin-2-one
  • Example 198 l-(6-chloro-benzo[l 5 3]dioxol-5-ylmethyl)-4-(thiazol-4-ylmethoxy)-lH- pyridin-2-one 1 B. NMR (CDCl 3 , 300 MHz) ⁇ 5.12 (s, 2H), 5.21 (s, 2H), 5.98 (s, 2H), 6.01 (dd, IH), 6.07 (d, IH) 5 6.86 (d, 2H), 7.24 (d, IH), 7.43 (s, IH), 8.87 (s, IH)
  • Example 200 pentanoic acid l-(6 ⁇ chloro-benzo[l,3]dioxol-5-ylmethyl)-2-oxo-l,2- dihydro-pyridin-4-yl ester
  • Example 201 hexanoic acid l-(6-chloro-benzo[l,3]dioxol-5-ylmethyl)-2-oxo-l,2- dihydro-pyridin-4-yl ester
  • Example 202 1 -(2-chloro-3-trifluoromethyl-benzyl)-4-pentyloxy-lH-pyridin-2-one 1 H NMR (CDCl 3 , 300 MHz) ⁇ 0.95 (t, 3H) 5 1.37-1.45 (m 5 4H), 1.78-1.81 (m, 2H), 3.94 (t 5 2H) 5 5.25 (s, 2H), 5.95-5.98 (m, 2H), 7.19-7.38 (m, 3H), 7.65 (d, IH)
  • Example 203 thiophene-2-carboxyl acid l-(6 ⁇ chloro-benzo[l,3]dioxol-5-ylmethyl)-2 ⁇ oxo- 1 ,2-dihydro-pyridin-4-yl ester
  • Example 204 toluene-4-sulfonic acid l-(6-chloro-benzo[l,3]dioxol-5-ylmethyl)-2-oxo-
  • Example 205 l-(6-chloro-benzo[l ,3]dioxol-5-ylmethyl)-4 ⁇ (4,4,5 5 5,5-pentafluoro- pentyloxy)- 1 H-pyridin-2-one
  • Example 206 1 -(6-chloro ⁇ benzo[l ,3]dioxol-5-ylmethyl)-4-(2-dimethylamino ⁇ ethoxy)-
  • Example 210 3-[l-(2,4-dichloro-benzyl)-2-oxo ⁇ l,2-dihydro-pyridin-4-yloxymethyl]- indole- 1 -carboxyl acid tetra-butyl ester
  • Example 211 1 -(2,4-dichloro-benzyl)-4-(2-thiophen-2-yl-ethoxy)- 1 H-pyridin-2-one 1 H NMR (CDCl 3 , 300 MHz) ⁇ 3.30 (t, 2H), 4.15 (t, 2H), 5.13 (s, 2H), 5.90-5.97 (m, 2H), 6.87-6.98 (m, 2H), 7.15-7.22 (m, 4H), 7.41 (s, IH)
  • Example 212 l-(2,4-dichloro-benzyl)-4-(2-thiophen-3-yl-ethoxy)-lH-pyridin-2-one 1 H NMR (CDCl 3 , 300 MHz) ⁇ 3.12 (t, 2H), 4.15 (t, 2H), 5.12 (s, 2H), 5.88-5.97 (m, 2H), 6.95-7.41 (m, 7H)
  • Example 215 1 -(3-amino-2-methyl-benzyl)-4-(2-thiophen-2-yl-ethoxy)-lH-pyridin-2- one
  • Example 216 1 -(3-amino-2-methyl-benzyl)-4-(2-pyrrol- 1 -yl-ethoxy)- 1 H-pyridin-2-one 1 H NMR (CDCl 3 , 300 MHz) ⁇ 2.01 (s, 3H), 4.16 (t, 2H), 4.25 (t, 2H), 5.04 (s, 2H), 5.83 (dd, IH), 5.90 (d, IH), 6.16 (t, 2H), 6.57 (d, IH), 6.71-6.75 (m, 3H), 6.91 (d, IH), 7.02 (t, IH)
  • Example 217 l-(3-amino-2-methyl-benzyl)-4-[2-(4-methyl-thiazol-5-yl)-ethoxy]-lH- pyridin-2-one 1 H NMR (CDCl 3 , 300 MHz) ⁇ 1.98 (s, 3H), 2.40 (s, 3H), 3.20 (t, 2H), 3.46 (br s, 2H), 4.06 (t, 2H), 5.02 (s, 2H), 5.81 (dd, IH), 5.92 (d, IH), 6.53 (d, IH), 6.68 (d, IH), 6.91 (d, IH), 6.99 (t, IH), 8.56 (s, IH)
  • Example 218 l-(3-Amino-2-methyl-benzyl)-4-(2-(5-bromothiophen-2-yl)-ethoxy)-lH- pyridin-2-one
  • Example 220 1 -[3-(2-Hydroxy-ethylamino)-2-methyl-benzyl]-4-(2-thiophen-2-yl- ethoxy)- 1 H-pyridin-2-one
  • Example 221 2- ⁇ 2-Methyl-3-[2-oxo-4-(2-thiophene-2-yl-ethoxy)-2H-pyridin-l - ylmethyl] -phenylamino ⁇ -acetamide 1 H NMR (CDCl 3 , 300 MHz) ⁇ 2.01 (s, 3H), 3.22 (t, 2H), 3.60 (d, 2H), 4.17 (t, 2H), 4.97 (s, 2H), 5.86 (m, IH), 5.94 (dd, IH), 6.20 (d, IH), 6.29 (d, IH), 6.95 (m, 3H), 7.33 (m, 2H)
  • Example 222 1 -[3-(Cyclopropylmethyl-amino)-2-methyl-benzyl]-4-(2-thiophen-2-yl- ethoxy)- 1 H-pyridin-2-one
  • Example 225 l-[2-Methyl-3-(2-pyrrol-l-yl-ethylamino)-benzyl]-4-(2-thiophen-2-yl- ethoxy)- 1 H-pyridin-2-one 1 H NMR (CDCl 3 , 300 MHz) ⁇ 1.85 (s, 3H), 3.28 (t, 2H), 3.51 (t, 3H) 5 4.14 (t, 4H), 5.05 (s, 2H), 5.84 (dd, IH), 5.93 (d, IH) 5 6.17 (m, 2H), 6.56 (d, IH), 6.65 (m, 3H), 6.90 (m, 3H), 7.10-7.17 (m, 2H)
  • Example 227 to 230 The procedure of Example 226 was repeated except the starting material to obtain the titled compound.
  • Example 227 l-[2-Methyl-3-(2-oxo-2-piperidin-l-yl-ethylamino)-benzyl]-4-(2- thiophen-2-yl-ethoxy)- 1 H-pyridin-2-one
  • Example 229 l- ⁇ 2-Methyl-3-[2-(4-methyl-piperazin-l-yl)-2-oxo-ethylamino]-benzyl ⁇ - 4-(2-thiophen-2-yl-ethoxy)- 1 H-pyridin-2-one
  • Example 230 l-[2-Methyl-3-(2-morpholin-4-yl-2-oxo-ethylamino)-benzyl]-4-(2- thiophen-2-yl-ethoxy)- 1 H-pyridin-2-one
  • Example 231 to 266 The procedure of Example 1 was repeated except the starting material to obtain the titled compound.
  • Example 231 1 -(3 - Amino-2-methyl-benzyl)-4-(2-furan-2-yl-ethoxy)- 1 H-pyridin-2-one 1 U NMR (CDCl 3 , 300 MHz) ⁇ 2.01 (s, 3H), 3.10 (t, 2H), 4.17 (t, 2H), 5.05 (s, 2H) 5 5.81 (dd, IH), 5.95 (d, IH), 6.10 (d, IH) 5 6.30 (d, IH), 6.57 (d, IH) 5 6.69 (d, IH), 6.90 (d, IH) 5 7.02(t, IH) 5 7.29 (d, IH)
  • Example 232 l-(3-Amino-2-methyl-benzyl)-4-[2-(5-methyl-thiophen-2-yl)-ethoxy]- lH-pyridin-2-one
  • Example 233 1 -(3-Amino-2-methyl-benzyl)-4-[2-(5-chloro-thiophen-2-yl)-ethoxy]- lH-pyridin-2-one
  • Example 234 l-(2,4-dichloro-benzyl)-4-[2-(3-methyl-thiophen-2-yl)-ethoxy]-lH- pyridin-2-one
  • Example 235 1 -(3 - Amino-2-methyl-benzyl)-4-(2-benzo [b]thiophen-3-yl-ethoxy)- 1 H- pyridin-2-one
  • Example 236 1 -(3-Amino-2-methyl-benzyl)-4-[2-(5-chloro-3-methyl- benzo [b]thiophen-2-yl)-ethoxy] - 1 H-pyridin-2-one 1 H NMR (CD 3 OD + a few drop of CDCl 3 , 300 MHz) ⁇ 1.97 (s, 3H), 2.32 (s, 3H), 3.32 (t, 2H), 4.20 (t, 2H), 5.01 (s, 2H), 5.92-5.97 (m, 2H), 6.45 (d, IH), 6.71 (d, IH), 6.96 (t, IH), 7.02 (d, IH), 7.21 (dd, IH), 7.55 (d, IH), 7.65 (d, IH)
  • Example 237 l-(3-amino-2-methyl-benzyl)-4-[2-(3-methyl-benzo[b]thiophen-2-yl)- ethoxy]-lH-pyridin-2-one
  • Example 239 1 -(3-Amino-2-methyl-benzyl)-4- [2-(5-ethyl-furan-2-yl)-ethoxy] - 1 H- pyridin-2-one
  • Example 240 5-[l -(3-amino-2-methyl-benzyl)-2-oxo-l ,2-dihydro-pyridin-4- yloxymethyl]-furan-2-carboxylic acid ethyl ester 1 H NMR (CDCl 3 , 300 MHz) ⁇ 1.37 (t, 3H) 5 2.00 (s, 3H) 5 4.36 (q, 2H) 5 4.97 (s, 2H), 5.05 (S 5 2H) 5 5.84 (dd 5 IH) 5 6.01 (d, IH) 5 6.55-6.58 (m, 2H), 6.69 (d, IH) 5 6.93 (d, IH) 5 7.02 (UH). 7.14 (d, IH)
  • Example 241 l-[3-(2-dimethylamino-ethylamino)-2-methyl-benzyl]-4-(2-thiophen-2- yl-ethoxy)- 1 H-pyridin-2 -one
  • Example 242 l-(3-amino-2-methyl-benzyl)-4-[2-(5-methylsulfanyl-thiophen-2-yl)- ethoxy] - 1 H-pyridin-2-one
  • Example 244 1 -(3-amino-2-methyl-benzyl)-4-[2-(3-methyl-isoxazol-5-yl)-ethoxy]-lH- pyridin-2-one 1 H NMR (CDCl 3 +a few drop of CD 3 OD, 300 MHz) ⁇ 1.86 (s, 3H), 1.93 (s, 3H), 2.63 (t, 2H), 4.14 (t, 2H), 4.96 (s, 2H), 5.82 (dd, IH), 5.90 (d, IH), 6.46 (d, IH), 6.64 (d, IH), 6.86 (d, IH), 6.94 (t, IH), 7.26 (s, IH)
  • Example 245 l-(3-amino-2-methyl-benzyl)-4-[2-(4,5-dimethyl-thiophen-2-yl)- ethoxy]- 1 H-pyridin-2-one
  • Example 246 l-(3-amino-2-methyl-benzyl)-4-[2-(5-ethyl-thiophen-2-yl)-ethoxy]-lH- pyridin-2-one
  • Example 247 1 -(3-amino-2,6-dichloro-benzyl)-4-(2-thiophen-2-yl-ethoxy)- 1 H- pyridin-2-one
  • Example 249 l-[2-methyl-3-(2-piperidin-l -yl-ethylamino)-benzyl]-4-(2-thiophen-2-yl- ethoxy)-lH-pyridin-2-one
  • Example 250 1 -[2-methyl-3-(2-morpholin-4-yl-ethylamino)-benzyl]-4-(2-thiophen-2- yl-ethoxy)- lH-pyridin-2-one
  • Example 251 N- ⁇ 2-methyl-3-[2-oxo-4-(2-thiophen-2-yl-ethoxy)-2H-pyridin-l- ylmethyl] -phenyl ⁇ -methanesulfonamide
  • Example 252 1 -(3-amino-2-methyl-benzyl)-4-[2-(4-bromo-thiophen-2-yl)-ethoxy]-lH- pyridin-2-one 1 H NMR (CDCl 3 , 300 MHz) ⁇ 1.99 (s, 3H) 5 3.22 (t, 2H) 5 3.69 (br S 5 2H) 5 4.10 (t, 2H), 5.04 (S 5 2H) 5 5.83 (dd, IH) 5 5.92 (d, IH) 5 6.55 (d, IH) 5 6.68 (d, IH), 6.80 (s, IH), 6.91 (d, IH), 6.98-7.06 (m, 2H)
  • Example 253 l-(6-chloro-benzo[l,3]dioxol-5-ylmethyl)-4-(2-pyrrol-l-yl-ethoxy)-lH- pyridin-2-one
  • Example 254 1 -(6-chloro-benzo[l ,3]dioxol-5-ylmethyl)-4-(2-thiophen-2-yl-ethoxy)- lH-pyridin-2-one
  • Example 255 1 -[2-methyl-3-(2-pyrrolidin- 1 -yl-ethylamino)-benzyl]-4-(2-thiophen-2- yl-ethoxy)- 1 H-pyridin-2-one
  • Example 257 l- ⁇ 2-methyl-3-[(pyridin-3-ylmethyl)-amino]-benzyl ⁇ -4-(2-thiophen-2- yl-ethoxy)-lH-pyridin-2-one
  • Example 259 l- ⁇ 2-methyl-3-[(pyridin-4-ylmethyl)-amino]-benzyl ⁇ -4-(2-thiophen-2- yl-ethoxy)- lH-pyridin-2-one
  • Example 260 l- ⁇ 2-methyl-3-[(thiazol-4-ylmethyl)-amino]-benzyl ⁇ -4-(2-thiophen-2-yl- ethoxy)- 1 H-pyridin-2-one
  • Example 261 1 -[3-(4-methoxy-benzyloxy)-2-methyl-benzyl]-4-(2 ⁇ thiophen-2-yl ⁇ ethoxy)- 1 H-pyridin-2-one 1 H NMR (CDCl 3 , 300 MHz) ⁇ 2.15 (s, 3H), 3.29 (t, 2H), 3.81 (s, 3H), 4.16 (t, 2H), 4.99 (s, 2H), 5.08 (s, 2H), 5.88 (dd, IH), 6.00 (d, IH), 6.68 (d, IH), 6.90-6.96 (m, 6H), 7.11- 7.18 (m, 2H), 7.35 (d, 2H)
  • Example 262 1 - ⁇ 3-[(3.5-dimethyl-isoxazol-4-ylmethyl)-amino]-2-methyl-benzyl ⁇ -4- (2-thiophen-2-yl-ethoxy)- 1 H-pyridin-2-one
  • Example 264 l- ⁇ 2-methyl-3-[(l-methyl-pyrrolidin-2-ylmethyl)-amino]-benzyl ⁇ -4-(2- thiophen-2-yl-ethoxy)- 1 H-pyridin-2-one
  • Example 265 l- ⁇ 2-methyl-3-[2-(l-methyl-pyrrolidin-2-yl)-ethylamino]-benzyl ⁇ -4-(2- thiophen-2-yl-ethoxy)- 1 H-pyridin-2-one
  • Example 266 (2- ⁇ 2-methyl-3-[2-oxo-4-(2-thiophen-2-yl-ethoxy)-2H-pyridin-l- ylmethyl]-phenylamino ⁇ -ethyl)-phosphonic acid diethyl ester
  • Example 267 4-(isobutylthio)- 1 -(2-methyl-3-nitrobenzyl)pyridin-2(l H)-one
  • 4-(isobutylthio)-l-(2-methyl-3-nitrobenzyl)pyridine-2(l/2')- one A mixture of lOOmg of 4-(isobutylthio)pyridine-2(lH)-one, 2ml of DMF, 65mg of t-BuOK was stirred at room temperature and 105mg of 2-methyl ⁇ 3-nitrobenzyl chloride was added. After 3 hour, the resulting solution was evaporated, extracted with dichloromethane and subjected to silica gel column chromatography(hexane/ethyl acetate) to obtain the compound (90mg).
  • Examples 268 to 280 The procedure of Example 267 was repeated except the starting material to obtain the titled compound.
  • Example 268 l-(3-amino-2-methylbenzyl)-4-(isobutylthio)pyridin-2(lH)-one A mixture of 400mg of l-(3 ⁇ amino-2-methylbenzyl)-4-(isobuthylthio)pyridin-
  • Example 269 1 -(3 -amino-2-methylbenzyl)-4-(furan-2-ylmethylthio)pyridine-2( 1 H)- one
  • MIC value was measured by conducting the following steps: diluting a test compound according to a two-fold dilution method; dispersing the resulting dilution in a M ⁇ ller-Hinton agar broth; inoculating 2 ml of the standard strain culture having a concentration of 10 7 cfu(colony forming unit)/ml; and incubating the mixture for 20 hrs at 37°C.
  • the resulting MIC values were in the range of 128 to 0.2 ⁇ g/ml, preferably, 1 to 0.2 ⁇ g/ml.

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Abstract

A compound which is effective for inhibiting Fab I, and a method for treating a bacterial infection.

Description

Fab I INHIBITOR AND PROCESS FOR PREPARING SAME
FIELD OF THE INVENTION
The present invention relates to a novel compound for inhibiting Fab I involved in bacterial fatty acid biosynthesis. This application claims priority under 35 U.S.C. 119(e) to the Provisional application filed on October 13, 2005 entitled "Novel Fab I Inhibitor And Process For Preparing Same," and to Provisional application 60/827,029 filed on September 26, 2006, both of which are hereby incorporated by reference. DESCRIPTION OF THE PRIOR ART Fatty acid synthase (FAS) is involved in the overall biosynthetic pathway of saturated fatty acids in all organisms, but the structural organization of FAS varies considerably among them. The distinctive characteristics of FAS of vertebrates and yeast are that all enzymatic activities are encoded on one or two polypeptide chains, and that the acyl carrier protein (ACP) exists in the form of a complex. In contrast, in bacterial FAS, each of synthetic steps is catalyzed by a distinct, mono-functional enzyme and the ACP is a discrete protein. Therefore, it is possible to selectively inhibit bacterial FAS by blocking one of the synthetic steps using an inhibitory agent.
NADH-dependent enoyl-ACP reductase (Fab I) is involved in the last step of the four reaction steps involved in each cycle of bacterial fatty acid biosynthesis. (See Payne et al, Drug Discovery Today 6, 2001, 537-544). The first step, the condensation of malonyl-ACP with acetyl-CoA (Fab H), is catalyzed by β-ketoacyl-ACP synthase. The second step is ketoester reduction by NADPH-dependent β-ketoacyl-ACP reductase (Fab G). Subsequent dehydration by β-hydroxyacyl-ACP dehydrase (Fab A or Fab Z) leads to trans-2-enoyl-ACP. Finally, in the fourth step, trans-2-enoyl-ACP is converted to acyl-ACP having two additional carbon atoms by Fab I. Such a cycle is repeated, eventually leading to palmitoyl-ACP (16C), whereupon the cycle is stopped due to inhibition of Fab I by palmitoyl-ACP (see Heath et al., J Biol, Chem. 271, 1996, 1833- 1836). Thus, Fab I is the biosynthetic enzyme in the overall synthetic pathway of bacterial fatty acid biosynthesis.
Recent studies have shown that Fab I is the target for a broad spectrum antibacterial agent such as triclosan (see McMurry et al., Nature, 1998, 394, 531-532) or diazaborine (see Baldock et al., Science, 1996, 274, 2107-2110). Also, diazaborine has been reported to function as an irreversible inhibitor of Fab I through the formation of a covalent complex with Fab I (see Baldock et al., Biochem. Pham. 1998, 55, 1541-1549), while triclosan is a reversible inhibitor of Fab I (see Ward et al., Biochem. 38, 12514- 12525).
PCT Publication No. WO 2001/027103 discloses Fab I inhibitors represented by the following formula or pharmaceutically acceptable salts thereof:
Figure imgf000003_0001
wherein,
Figure imgf000003_0002
Figure imgf000004_0001
Figure imgf000004_0002
B is H, C1-4 alkyl or C3-6 cycloalkyl;
Figure imgf000004_0003
D is H or Ci-4 alkyl;
E is CH2 when the bond to which it is attached is a double bond; or E is H or C 1.4 alkyl when the bond to which it is attached is a single bond, in which A is H or C1-4 alkyl; F is H or C1-4 alkyl; G is H, C1-4 alkyl or Co-6 alkylaryl; I is O orN R'2;
Q is H, Ci-4 alkyl, N(RZ)2, NHC(O)R', NHCH2C(O)R' Or NHC(O)CH=CHR'; X is each independently H, C1-4 alkyl, CH2OH, OR', SR', CN, N(RZ)2, CH2N(R')2, NO2, CF3, CO2R', CON(RZ)2, COR', F, Cl5 Br5 1 or -S(O)rCF3 (r is O, 1 or
2);
W is S or O; M is CH2 or O; L is CH2 or C(O); and
R' is each independently H5 Ci-4 alkyl or C0-6 alkylaryl.
In addition, PCT Publication Nos. WO 2004/052890 and WO 2004/064837 and Canadian Patent No. 2,444,957 disclose a Fab I inhibitor for bacterial treatment.
The present inventors have developed a novel Fab I inhibitor which has broad antibacterial activity against Gram positive bacteria including methicillin resistant Staphylococcus Aureus (MRSA).
SUMMARY OF THE INVENTION
It is an object of the present invention to provide a novel compound which efficiently inhibits Fab I and is useful for the treatment of bacterial infections.
In accordance with one aspect of the present invention, there is provided a compound of formula (I) or (II) or a pharmaceutically acceptable analog thereof selected from the group consisting of salt, acid, ester, amide, and nitrile:
Figure imgf000005_0001
CO
Figure imgf000006_0001
wherein,
Ri is selected from the group of radicals consisting of:
(a) H, (b) C1-8 alkyl, Ci-8 alkenyl, C1-8 alkynyl,
(c) aryl, C3-8 cycloalkyl, C3-8 cycloalkenyl,
(d) an analog of a radical of group (c) containing one or more heteroatoms selected from N, S or and O, and
(e) a substituted analog of a radical selected from the group consisting of groups (b), (c), and (d), said substituted analog containing one or more substituents selected from the group consisting of: hydroxyl, halogen, Cj-6 alkyl, C3-8 cycloalkyl, C3-8 heterocycloalkyl, alkyloxy, amino, alkylamino, carboxyl, nitro, sulfonylamide, alkylsulfonyl, amide, dioxoisoindole, trihaloalkyl, aryl, heteroaryl, substituted aryl, and substituted heteroaryl, wherein said substituted aryl and substituted heteroaryl contain one or more substituents selected from the group consisting of C1-6 alkyl, C3-8 cycloalkyl, C3-8 heterocycloalkyl, alkyloxy, amino, alkylamino, carboxyl, nitro, sulfonylamide, alkylsulfonyl, amide, dioxoisoindole, trihaloalkyl, aryl; A is selected from the group consisting of C-R2 and N; R2 is selected from the group consisting of H, Cj-5 alkyl, benzyl, and substituted C1-5 alkyl containing one or more substituents selected from the group consisting of methyl, ethyl, hydroxyl, hydroxylmethyl and hydroxylethyl;
B is selected from the group consisting of carbonyl, CH2 and NH; R4 is selected from the group of radicals consisting of:
(a) Ci-8 alkyl, Ci-8 alkenyl, Cj-8 alkynyl,
(b) aryl, C3-8 cycloalkyl, C3-8 cycloalkenyl,
(c) an analog of a radical of group (b) containing one or more heteroatoms selected from N5 S and O, and (d) a substituted analog of a radical selected from the group consisting of groups (a), (b), and (c), said substituted analog containing one or more substituents selected from the group consisting of: hydroxyl, halogen, C1-6 alkyl, C3-8 cycloalkyl, C3-8 heterocycloalkyl, alkyloxy, amino, alkylamino, carboxyl, nitro, sulfonylamide, alkylsulfonyl, amide, dioxoisoindole, trihaloalkyl, aryl, heteroaryl, substituted aryl, and substituted heteroaryl, wherein said substituted aryl and substituted heteroaryl contain one or more substituents selected from the group consisting of: Cμ6 alkyl, C3-8 cycloalkyl, C3-8 heterocycloalkyl, alkyloxy, amino, alkylamino, carboxyl, nitro, sulfonylamide, alkylsulfonyl, amide, dioxoisoindole, trihaloalkyl, and aryl;
W is selected from the group consisting of C-R6 and N; Z is selected from the group consisting of C-R5 and N;
R5 and R6 are each independently selected from the group consisting of H, halogen, C1-5 alkyl, and substituted C1-5 alkyl containing one or more substituents selected from the group consisting of methyl, ethyl, hydroxyl, hydroxylmethyl and hydroxylethyl; and X is selected from C, N, O and S.
DETAILED DESCRIPTION OF THE INVENTION In accordance with one aspect of the present invention, there is provided a novel compound of formula (I) or (II), or a pharmaceutically acceptable salt thereof.
The term "heteroaryl" as used herein means an aryl group containing one or more heteroatoms selected from N, S or O in the ring structure. Exemplary heteroaryls include those derived from pyrrole, pyrazole, imidazole, 1,2,3-triazole, 1,2,4-triazole, furan, isoxazole, oxazole, thiophene, isothiazole, thiazolidine, thiazole, 1,2,5-oxadiazole, 1,2,3- oxadiazole, 1,2,5-thiodiazole, 1,2,3-thiodiazole, 1,3,4-oxadiazole, 1,3,4-thiodiazole, pyridine, pyrimidine, tetrazole and triazine.
The term "bacteria-related diseases" as used herein means illnesses or conditions which are caused by bacterial infection and may be alleviated or relieved by a Fab I inhibitor treatment, and may include but are not limited to urinary tract, respiratory or skin tissue infections, sepsis, etc.
It is to be understood that the inventive compound may contain asymmetric centers of R or S configuration and thus the present invention includes geometrical isomers, stereoisomers and racemic mixtures of the compound of formula (I) or (II). The pharmaceutically acceptable salt of the inventive compound which may be a non-toxic addition salt may be prepared by using an acid or base. Exemplary acids which may be used in the present invention include such inorganic acids as hydrochloric, hydrobromic, phosphoric and sulfuric acid; and an organic acid such as an organic carboxylic acid, e.g., acetic, trifluoroacetic, citric, formic, maleic, oxalic, succinic, benzoic, tartaric, fumaric, mandelic, ascorbic and malic acid, methanesulfonic acid and /?-toluenesulfonic acid. Exemplary bases which may be used in the present invention include such inorganic bases as an alkali metal hydroxide (e.g., sodium hydroxide and potassium hydroxide), an alkali metal bicarbonate (e.g., sodium bicarbonate and potassium bicarbonate), an alkali metal carbonate (e.g., sodium carbonate, potassium carbonate and calcium carbonate) and an organic base such as amines.
The inventive compound may also be used in the form of a pharmaceutically acceptable derivative or prodrug which has a suitable ester or amide group. Preferable examples of the ester which can be hydrolyzed chemically or biochemically in the living body include indanyl, phthalidyl, pivaloyloxymethyl, glycyloxymethyl, phenylglycyloxymethyl, and 5-methyl-2-oxo-l,3-dioxorene-4-ylmethyl esters.
The preferred compounds of the present invention are as follows:
4-benzyloxy- 1 -(2-chloro-benzyl)- 1 H-pyridin-2-one ; 4-benzyloxy- 1 -(4-chloro-benzyl)- 1 H-pyridin-2-one;
4-benzyloxy-l-(4-nitro-benzyl)-lH-pyridin-2-one;
4-benzyloxy- 1 -(2,5-dichIoro-benzyl)- 1 H-pyridin-2-one;
4-benzyloxy- 1 -(2,4-dichloro-benzyl)- 1 H-pyridin-2-one;
4-benzyloxy-2-(4-methoxy-benzyloxy)-pyridine; 4-benzyloxy-l-(4-methoxy-benzyl)-lH-pyridin-2-one;
4-benzyloxy-2-(4-methyl-benzyloxy)-pyridine;
4-benzyloxy- 1 -(4-methyl-benzyl)- 1 H-pyridin-2-one;
4-benzyloxy- 1 -(6-chloro-pyridin-3 -ylm ethyl)- 1 H-pyridin-2-one;
4-benzyloxy- 1 -(3-chloro-benzyl)- 1 H-pyridin-2-one; 1 -benzyl-4-benzyloxy- 1 H-pyridin-2-one;
1 -(4-amino-benzyl)-4-benzyloxy- 1 H-pyridin-2-one; l-(2,4-dichloro-benzyl)-4-hydroxy-l H-pyridin-2-one;
3-benzyl-l-(2,4-dichloro-benzyl)-4-hydroxy-lH-pyridin-2-one; 4-(biphenyl-4-ylmethoxy)-l-(2,4-dichloro-benzyl)-lH-pyridin-2-one;
1 -(2,4-dichloro-benzyl)-4-(2,4-dichloro-benzyloxy)- 1 H-pyridin-2-one;
4-(2-chloro-benzyloxy)-l-(2,4-dichloro-benzyl)-lH-pyridin-2-one; l-(2,4-dichloro-benzyl)-4-methoxy-lH-pyridin-2~one;
1 -(2,4-dichloro-benzyl)-4-isopropoxy- 1 H-pyridin-2-one; 4-cyclohexylmethoxy-l-(2,4-dichloro-benzyl)-lH-pyridin-2-one; l-(2,4-dichloro-benzyl)-4-propoxy-lH-pyridin-2-one; l-(2,4-dichloro-benzyl)-4-isobutoxy-lH-pyridin-2-one;
4-butoxy- 1 -(2,4-dichloro-benzyl)- 1 H-pyridin-2-one;
1 -(2,4-dichloro-benzyl)-4-octyloxy- 1 H-pyridin-2-one; 1 -(2,4-dichloro-benzyl)-4-(4-methyl-pentoxy)- 1 H-pyridin-2-one;
4-(but-3 -enyloxy)- 1 -(2,4-dichloro-benzyl)- 1 H-pyridin-2-one; l-(2,4-dichloro-benzyl)-4-pentyloxy-lH-pyridin-2-one;
[l-(2,4-dichloro-benzyl)-2-oxo-l,2-dihydro-pyridin-4-yloxy]-acetic acid ethylester; 1 -(2,4-dichloro-benzyl)-4-(3-methyl-butoxy)- 1 H-pyridin-2-one;
1 -benzyl-4-pentyloxy- 1 H-pyridin-2-one;
1 -(2-chloro-benzyl)-4-pentyloxy- 1 H-pyridin-2-one;
4-pentyloxy- 1 -propyl- 1 H-pyridin-2-one;
1 -butyl-4-pentyloxy- 1 H-pyridin-2 -one; 1 -isobutyl-4-pentyloxy- 1 H-pyridin-2-one;
1 -(3-methyl-butyl)-4-pentyloxy- 1 H-pyridin-2-one;
1 -(2,4-dichloro-benzyl)-4-hexyloxy- 1 H-pyridin-2-one;
1 -(2,4-dichloro-benzyl)-4-heptyloxy- 1 H-pyridin-2-one; 1 -(4-chloro-benzyl)-4-pentyloxy- 1 H-pyridin-2-one; -aryloxy- 1 -(2,4-dichloro-benzyl)- 1 H-pyridin-2-one; l-(2,4-dichloro-benzyl)-4-(3-methoxy-propoxy)-lH-pyridin-2-one; l-(2,4-dichloro-benzyl)-4-(3-ethylamino-propoxy)-lH-pyridin-2-one; l-(2,4-dichloro-benzyl)-4-(2-ethoxy-ethoxy)-lH-pyridin-2-one; 1 -(3-methyl-but-2-enyl)-4-pentyloxy- 1 H-pyridin-2-one;
4-pentyloxy- 1 -thiazol-4-ylmethyl- 1 H-pyridin-2-one ; -pentyloxy- 1 -pyridin-3 -ylmethyl- 1 H-pyridin-2-one ; l-(2,4-dichloro-benzyl)-4-(4-methyl-pent-3-enyloxy)-lH-pyridin-2-one; l-(2,4-dichloro-benzyl)-4-(3-methoxy-proρoxy)-lH-pyridin-2-one; 1 -(2,4-dichloro- benzyl)-4-phenetyloxy- 1 H-pyridin-2-one; l-(2-methyl-benzyl)-4-pentyloxy-lH-pyridin-2-one;
4-pentyl-l-phenetyl-lH-pyridin-2-one;
1 -(2,4-dichloro-5 -fluoro-benzyl)-4-pentyloxy- 1 H-pyridin-2-one;
1 -(3 ,4-dichloro-benzyl)-4-pentyloxy- 1 H-pyridin-2-one; 1 -(3 ,4-difluoro-benzyl)-4-pentyloxy- 1 H-pyridin-2-one;
4-(4-benzyloxy-butoxy)- 1 -(2,4-dichloro-benzyl) - 1 H-pyridin-2-one;
1 -(2,4-dichloro-benzyl)-4-(4~hydroxy-butoxy)- 1 H-pyridin-2-one;
4-(5-benzyloxy-pentyloxy)- 1 -(2,4-dichloro-benzyl)- 1 H-pyridin-2-one;
1 -(2,4-dichloro-benzyl)-4-(5-hydroxy-pentyloxy)- 1 H-pyridin-2-one; l-(6-chloro-benzo[l,3]dioxol-5-ylmethyl)-4-pentyloxy-lH-pyridin-2-one;
1 -(2,4-dichloro-benzyl)-4-(2-methyl-benzyloxy)- 1 H-pyridin-2-one; l-(2,4-dichloro-benzyl)-4-(4-methyl-benzyloxy)-lH-pyridin-2-one;
1 -(2-nitro-benzyl)-4-pentyloxy- 1 H-pyridin-2-one; l-(2-amino-benzyl)-4-pentyloxy-l H-pyridin-2-one;
N-[2-(2-oxo-4-pentyloxy-2H-pyridin-l-ylmethyl)-phenyl]-acetamide;
4-pentyloxy-l-(2-trifluoromethyl-benzyl)-lH-pyridin-2-one;
N- [4-(4-benzyloxy-2-oxo-2H-pyridin- 1 -ylmethyl)-phenyl] acetamide ; l-(2,4-dichloro-benzyl)-4-(naphthalen-2-ylmethoxy)-lH-pyridin-2-one; 1 -naphthalen-2-ylmethyl-4-pentyloxy~lH-pyridin-2-one;
4-benzyloxy-l-(6-chloro-benzo[l,3]dioxol-5-ylmethyl)-lH-pyridin-2-one; l-(6-chloro-benzo[l,3]dioxol-5-ylmethyl)-4-(3-methyl-butoxy)-lH-pyridin-2- one; l-(2-methyl-benzyl)-4-(3-methyl-butoxy)-lH-pyridin-2-one; 4-(3-methyl-butoxy)- 1 -(2-nitro-benzyl)- 1 H-pyridin-2-one; l-(2,4-dichloro-benzyl)-4-pentylamino-lH-pyridin-2-one;
1 -(2,3-dichloro-benzyl)-4-pentyloxy- 1 H-pyridin-2-one;
1 -(2-methoxy-benzyl)-4-pentyloxy- 1 H-pyridin-2-one; l-(2,3-dimethoxy-benzyl)-4-pentyloxy-lH-pyridin-2-one; 4-(5 -benzyloxy-pentyloxy)- 1 -(6-chloro-benzo [ 1 ,3]dioxol-5-ylmethyl)- 1 H- pyridin-2-one;
1 -(2-chloro-benzyl)-4-(3-methyl-butoxy)- 1 H-pyridin-2-one; l-(3,4-dichloro-benzyl)-4-(3-methyl-butoxy)-lH-pyridin-2-one; l-(2,4-dichloro-5-fluoro-benzyl)-4-(3-methyl-butoxy)-lH-pyridin-2-one; 1 -benzyl-4-(3 -methyl-butoxy)- 1 H-pyridin-2-one;
1 -(4-chloro-benzyl)-4-(3-methyl-butoxy)- 1 H-pyridin-2-one; l-(2,4-dichloro-benzyl)-4-pentyloxy-lH-pyrimidin-2-one;
1 -(2,4-dichloro-benzyl)-4-(4-methyl-pentyloxy)- 1 H-pyrimidin-2-one; 1 -(2,4-dichloro-benzyl)-4-phenoxy- 1 H-pyrimidin-2-one;
4-(butyl-methyl-amino)-l-(2,4-dichloro-benzyl)-lH-pyrimidin-2-one; l-(2,4-dichloro-benzyl)-4-(2-diethylamino-ethoxy)-lH-pyrimidin-2-one;
4-butoxy-l-(2,4-dichloro-benzyl)-lH-pyrimidin-2-one; l-(2,6-dichloro-benzyl)-4-pentyloxy-lH-pyridin-2-one; 1 -(2-chloro-6-fluoro-benzyl)-4-pentyloxy-lH-pyridin-2-one;
1 -(2-methyl~3-nitro-benzyl)-4-pentyloxy- lH-pyridin-2-one;
1 -(3 -amino-2-methyl-benzyl)-4-pentyloxy- 1 H-pyridin-2-one ; l-(4-metrioxy-3,5-dimethyl-pyridin-2-ylmethyl)-4-pentyloxy-lH-pyridin-2-one; l-(6-chloro-benzo[l,3]dioxol-5-ylmethyl)-4-(5-hydroxy-pentyloxy)-lH-pyridin- 2-one;
1 -(2-methoxy-5-nitro-benzyl)-4-pentyloxy- lH-pyridin-2-one; l-(5-amino-2-methoxy-benzyl)-4-pentyloxy-lH-pyridin-2-one; l-(2-ethyl-benzyl)-4-pentyloxy-lH-pyridin-2-one;
1 -(2-chloro-5-nitro-benzyl)-4-pentyloxy- 1 H-pyridin-2-one; 1 -(5-amino-2-chloro-benzyl)-4-pentyloxy- 1 H-pyridin-2-one;
1 -(4-methoxy-2,3 -dimethyl-benzyl)-4-pentyloxy- 1 H-pyridin-2-one; l-(2-methyl-pyridin-3-ylmethyl)-4-pentyloxy-lH-pyridin-2-one;
N-[4-chloro-3-(2-oxo-4-pentyloxy-2H-pyridin-l-ylmethyl)-phenyl]-acetamide; l-(2,4-dichloro-benzyl)-4-(3-dimethylamino-propoxy)-lH-pyridin-2-one; 1 -(2,4-dichloro-benzyl)-4-(4-dimethylamino-butoxy)- 1 H-pyridin-2-one;
1 -(2,4-dichloro-benzyl)-4-(6-dimethylamino-hexyloxy)- 1 H-pyrimidin-2-one;
1 -(2,4-dimethyl-benzyl)-4-pentyloxy- 1 H-pyridin-2-one;
1 -(2-chloro-5-trifluorom ethyl -benzyl)-4-pentyloxy- 1 H-pyridin-2-one; 1 -(2-hydroxy~benzyl)-4-pentyloxy~ 1 H-pyridin-2-one;
4-(3-cyclo-propoxy)-l-(2,4-dichloro-benzyl)-lH-pyrimidin-2-one; l-(2,4-dichloro-benzyl)-4-(3-methyl-pentyloxy)-lH-pyrimidin-2-one; l-(2,4-dichloro-benzyl)-4-hex-4-enyloxy-lH-pyrimidin-2-one;
4-(2-cyclopropyl-ethoxy)-l-(2,4-dichloro-benzyl)-lH-pyrimidin-2-one; l-(2,4-dichloro-benzyl)-4-(3-methyl-pentyloxy)-lH-pyridin-2-one; l-(2,4-dichloro-benzyl)-4-(5-morpholin-4-yl-pentyloxy)-lH-pyridin-2-one; l-(2-chloro-5-methoxy-benzyl)-4-pentyloxy-lH-pyridin-2-one; l-(2-chloro-5-ethoxy-benzyl)-4-pentyloxy-lH-pyridin-2-one; l-(2-chloro-5-propoxy-benzyl)-4-pentyloxy-lH-pyridin-2-one; l-[2-chloro-5-(2-hydroxy-ethoxy)-benzyl]-4-pentyloxy-lH-pyridin-2-one;
[4-chloro-3-(2-oxo-4-pentyloxy-2H-pyridin-l-ylmethyl)-oxy]-acetonitrile;
1 - [5 -(2-amino-ethoxy)-2-chloro-benzyl] -4-pentyloxy- 1 H-pyridin-2-one ;
N-[2-methyl-3-(2-oxo-4-pentyloxy-2H-pyridin-l-ylmethyl)-phenyl]-acetamide;
1 -(2-methyl-3 -methylamino-benzyl)-4-phenyloxy- 1 H-pyridin-2-one; 1 -(3-dimethylamino-2-methyl-benzyl)-4-ρhenyloxy- 1 H-pyridin-2-one;
1 -(3-ethylamino-2-methyl-benzyl)-4-pentyloxy- 1 H-pyridin-2-one; l-(3-diethylamino-2-methyl-benzyl)-4-pentyloxy-lH-pyridin-2-one; l-(2-methyl-3-propylamino-benzyl)-4-pentyloxy-lH-pyridin-2-one; l-(3-dipropylamino-2-methyl-benzyl)-4--pentyloxy-lH-pyridin-2-one; 1 -[3 -(2-hydroxy-ethylamino)-2-methyl-benzyl] -4-pentyloxy- 1 H-pyridin-2-one; l-(2-chloro-5-methoxy-4-nitro-benzyl)-4-pentyloxy-lH-pyridin-2-one;
1 -(4-amino-2-chloro-5-methoxy-benzyl)-4-pentyloxy- 1 H-pyridin-2-one;
N- [5-chloro-2-methoxy-4-(2-oxo-4-pentyloxy-2H-pyridin- 1 -ylmethyl)-phenyl] - acetamide; l-(2-chloro-5-methoxy-4-methylamino-benzyl)-4-pentyloxy-lH-pyridin-2-one; l-(2-chloro-4-dimethylamino-5-methoxy-benzyl)-4-pentyloxy-lH-pyridin-2- one; l-(2-chloro~4-ethylamino-5-methoxy-benzyl)-4-pentyloxy-lH-pyridin-2-one; l-(2-chloro-5-methoxy-4-propylamino-benzyl)-4-pentyloxy-lH-pyridin-2-one; l-[2-chloro-4-(2-hydroxy-ethylamino)-5-methoxy-benzyl]-4-pentyloxy-lH- pyridin-2-one; l-(4-amino-6-chloro-3-methoxy-2-nitro-benzyl)-4-pentyloxy-lH-pyridin-2-one;
1 -(2 J4-diamino-6-chloro-3-methoxy-benzyl)-4-pentyloxy- 1 H-pyridin-2-one; 1 -(2,5-dichloro-6-methoxy-pyrimidin-4-ylmethyl)-4-pentyloxy- 1 H-ρyridin-2- one;
1 -(2,4-dichloro-benzenesulfonyl)-4-pentyloxy- 1 H-pyridin-2-one;
1 -(4-methanesulfonyl-benzyl)-4-pentyloxy- 1 H-pyridin-2-one;
1 -(4-amino-2-chloro-5-hydroxy-benzyl)-4-pentyloxy- 1 H-pyridin-2-one; 4-(4-bromo-butoxy)- 1 -(2,4-dichloro-benzyl)- 1 H-pyridin-2-one;
4- [ 1 -(2,4-dichloro-benzyl)-2-oxo- 1 ,2-dihydro~pyridin-4-yloxy] - buty lammonium ; l-(5-chloro-2,6-dimethoxy-pyrimidin-4-ylmethyl)-4-pentyloxy-lH-pyridin-2- one; 1 -(2-amino-5-chloro-6-methoxy-pyrimidin-4-ylmethyl)-4-pentyloxy- 1 H- pyridin-2-one;
l-(6-amino-2,5-dichloro-pyrimidin-4-ylmethyl)-4-pentyloxy-lH-pyridin-2-one;
5-chloro-6-(2-oxo-4-pentyloxy-2H-pyridin-l-ylmethyl)-3H-benzoxazol-2-one; 1 -(2-chloro-4-hydroxy-benzyl)-4-pentyloxy- 1 H-pyridin-2-one;
1 -(2-chloro-4-isopropoxy-benzyl)-4-pentyloxy- 1 H-pyridin-2-one;
2-[3-(2-oxo-4-pentyloxy-2H-pyridin-l-yl)-propyl]-isoindole-l,3-dione; l-(3-amino-propyl)-4-pentyloxy-lH-pyridin-2-one;
N- [3 -(2-oxo-4-pentyloxy-2H-pyridin- 1 -yl)-propyl] -acetamide ; 1 -(3-dimethylamino-propyl)-4-pentyloxy-lH-pyridin-2-one; l-(2,4-dichloro-benzyl)-6-methyl-4-pentyloxy-lH-pyridin-2-one; l-(2,4-dichloro-benzyl)-6-methyl-3-pentyl-4-pentyloxy-lH-pyridin-2-one;
1 -(2-amino-ethyl)-4-pentyloxy- 1 H-pyridin-2-one;
N-[2-(2-oxo-4-pentyloxy-2H-pyridm-l-yl)-ethyl]-acetamide; N-[I5I -dimethyl-2-(2-oxo-4-pentyloxy-2H-pyridin- 1 -yl)-ethyl]- methanesulfonamide;
N-[l-(2-oxo-4-pentyloxy-2H-pyridin-l-ylmethyl)-propyl]-methanesulfonamide; l-(7-nitro-benzo[l,3]dioxol-5-ylmethyl)-4-pentyloxy-lH-pyridin-2-one;
1 -(2-chloro-3 -nitro-benzyl)-4-pentyloxy- 1 H-pyridin-2-one; 1 -(3-amino-2-chloro-benzyl)-4-pentyloxy- 1 H-pyridin-2-one;
N- [2-chloro-3 -(2-oxo-4-pentyloxy-2H-pyridin- 1 -ylmethyl)-phenyl] -acetamide ;
N-[2-chloro-3-(2-oxo-4-pentyloxy-2H-pyridin-l-ylmethyl)-phenyl]- methanesulfonamide ;
N3N' - [2-chloro-3 -(2-oxo-4-pentyloxy-2H-pyridin- 1 -ylmethyl)-phenyl] - dimethanesulfonamide ;
l-[2-chloro-3-(2-hydroxy-ethylamino)-benzyl]-4-ρentyloxy-lH-pyridin-2-one;
4-chloro-2-(2-chloro-benzyl)-5-pentyloxy-2H-pyridazin-3-one;
2-(2-chloro-benzyl)-5-pentyloxy-2H-pyridazin-3-one; 1 -(3-amino-2,6-dichloro-benzyl)-4-pentyloxy- 1 H-pyridin-2-one; l-(3-benzyloxy-2-chloro-4-methoxy-benzyl)-4-pentyloxy-lH-pyridin-2-one; l-(2-chloro-3,4-dimethoxy-benzyl)-4-pentyloxy-lH-pyridin-2-one; l-(2-chloro-3-hydroxy-4-methoxy~benzyl)-4-pentyloxy-lH-pyridin-2-one; l-[2-chloro-4-methoxy-3-(2-methoxy-ethoxy)-benzyl]-4-pentyloxy-lH-pyridin- 2-one;
1 -[2-chloro-4-methoxy-3-(2-pyrrolidin- 1 -yl-ethoxy)-benzyl]-4-pentyloxy- 1 H- pyridin-2-one;
1 -[2-chloro-3-(2-dimethylamino-ethoxy)-4-methoxy-benzyl]-4-pentyloxy- 1 H- pyridin-2-one; 2-{3-[2-chloro-6-methoxy-3-(2-oxo-4-pentyloxy-2H-pyridin-l-ylmethyl)- phenoxyl]-propyl}-isoindole-l,3-dione; l-[3-(2-dimethylamino-ethoxy)-2-methyl-benzyl]-4-pentyloxy-lH-pyridin-2- one;
1 -[2-chloro-3-(2-dimethylamino-ethylamino)-benzyl]-4-pentyloxy- 1 H-pyridin- 2-one; l-[2,6-dichloro-3-(2-hydroxy-ethylamino)-benzyl]-4-pentyloxy-lH-pyridin-2- one; l-[2,6-dichloiO-3-(2-dimethylamino-ethylamino)-benzyl]-4-pentyloxy-lH- pyridin-2-one; l-[2,6-dichloro-3-(3-hydroxy-propylamino)-benzyl]-4-pentyloxy-lH-pyridin-2- one;
l-[2,6-dichloro-3-(3-dimethylamino-propylamino)-benzyl]-4-pentyloxy-lH- pyridin-2-one; l~[3-(3-amino-propylamino)~2,6-dichloro-benzyl]-4-pentyloxy-lH-pyridin-2- one; l-(3-fluoro-2-methyl-benzyl)-4-pentyloxy-lH-pyridin-2-one; l-(2-chloro-3-dimetb.ylaminomethyl-4-fluoro-benzyl)-4-ρentyloxy-lH-pyridin- 2-one; l-(2,6-dichloro-3-methylamino-benzyl)-4-pentyloxy-lH-pyridin-2-one; l-(2,6-dichloro-3-dimethylamino-benzyl)-4-pentyloxy-lH-pyridin-2-one;
[2-chloro-3-(2-oxo-4-pentyloxy-2H-pyridin-l-ylmethyl)-phenylamino]-acetic acid; l-(6-chloro-benzo[l,3]dioxol-5-ylmethyl)-4-(pyridin-4-ylmethoxy)-lH-pyridin- 2-one; l-(6-chloro-benzo[l,3]dioxol-5-ylmethyl)-4-(6-chloro-pyridin-3-ylmethoxy)- 1 H-pyridin-2-one ; l-(6-chloro-benzo[l,3]dioxol-5-ylmethyl)-4-(4-methoxy-3,5-dimethylpyridin-2- ylmethoxy) - 1 H-pyridin-2-one ; l-(6-chloro-benzo[l,3]dioxol-5-ylmethyl)-4-(2-methyl-pyridin-3-ylmethoxy)-
1 H-pyridin-2-one; l-(6-chloro-benzo[l,3]dioxol-5-ylmethyl)-4-(thiazol-4-ylmethoxy)-lH-pyridin-
2-one; l-(6-chloro-benzo[l,3]dioxol-5-ylmethyl)-4-(pyridin-2-ylmethoxy)-lH-pyridin- 2-one;
pentanoic acid l-(6-chloro-benzo[l ,3]dioxol-5-ylmethyl)-2-oxo-l,2-dihydro- pyridin-4-yl ester; hexanoic acid 1 ~(6-chloro-benzo[ 153]dioxol-5-ylmethyl)-2-oxo- 1 ,2-dihydro- pyridin-4-yl ester; l-(2-chloro-3-trifluoroniethyl-benzyl)-4-pentyloxy-lH-pyridin-2-one; thiophene-2-carboxyl acid 1 -(6-chloro-benzo[ 1 ,3]dioxol-5-ylmethyl)-2-oxo- 1 ,2- dihydro-pyridin-4-yl ester; toluene-4-sulfonic acid 1 -(6-chloro-benzo[ 1 ,3]dioxol-5-ylmethyl)-2-oxo- 1 ,2- dihydro-pyridin-4-yl ester; l-(6-chloro-benzo[ls3]dioxol-5-ylmethyl)-4-(4,4,5,5,5-pentafluoro-pentyloxy)- lH-pyridin-2-one; l-(6-chloro-benzo[l53]dioxol-5-ylmethyl)-4-(2-dimethylamino-ethoxy)-lH- pyridin-2-one; 1 -(2,4-dichloro-benzyl)-4-(5-fluoro-pentyloxy)- 1 H-pyridin-2-one;
3-[ 1 -(2,4-dichloro-benzyl)-2-oxo- 1 ,2-dihydro-pyridin-4-yloxymethyl]-indole- 1 - carboxyl acid tetra-butyl ester;
1 -(2,4-dichloro-benzyl)-4-(2-thiophen-2-yl-ethoxy)- 1 H-pyridin-2-one; l-(2,4-dichloro-benzyl)-4-(2-thiophen-3-yl-ethoxy)-lH-pyridin-2-one; l-(2,4-dichloro-benzyl)-4-(2-pyrrol-l-yl-ethoxy)-lH-pyridin-2-one; l-(2,4-dichloro-benzyl)-4-(3-pyrrol-l-yl-propoxy)-lH-pyridin-2-one; l-(3-amino-2-methyl-benzyl)-4-(2-thiophen-2-yl-ethoxy)-lH-pyridin-2-one; l-(3-amino-2-methyl-benzyl)-4-(2-pyrrol-l-yl-ethoxy)-lH-pyridin-2-one; l-(3-amino-2-methyl-benzyl)-4-[2-(4-metb.yl-thiazol-5-yl)-ethoxy]-lH- pyridin- 2-one;
l-(3-amino-2-methyl-benzyl)-4-(2-(5-bromothiophen-2-yl)-ethoxy)-lH-pyridin- 2-one;
l-(3-amino-2-methyl-benzyl)-4-(2-(5-fluorothiophen-2-yl)-ethoxy)-lH-pyridin- 2-one;
l-[3-(2-hydroxy-ethylamino)-2-methyl-benzyl]-4-(2-thiophen-2-yl-ethoxy)-lH- pyridin-2-one;
2- {2-methyl-3-[2-oxo-4-(2-thiophene-2-yl-ethoxy)-2H-pyridin- 1 -ylmethyl]- phenylamino } -acetamide ; l-[3-(cyclopropylmethyl-amino)-2-methyl-benzyl]-4-(2-thiophen-2-yl-ethoxy)- lH-pyridin-2-one;
N-{2-methyl-3-[2-oxo-4-(2-thiophen-2-yl-ethoxy)-2H-pyridin-l-ylmethyl]- phenylamino } -acetonitrile ;
N-(2-{2-methyl-3-[2^oxo-4-(2-thiophen-2-yl-ethoxy)-2H-pyridin-l-ylmethyl]- phenylamino } -ethyl)-acetamide ;
1 -[2-methyl-3-(2-pyrrol- 1 -yl-ethylamino)-benzyl]-4-(2-thiophen-2-yl-ethoxy)- lH-pyridin-2-one; l-[2-methyl-3-(2-oxo-2-pyrrolidin-l-yl-ethylamino)-benzyl]-4-(2-thiophen-2-yl- ethoxy)- 1 H-pyridin-2-one ; l-[2-methyl-3-(2-oxo-2-piperidin-l-yl-ethylamino)-benzyl]-4-(2-thiophen-2-yl- ethoxy)- 1 H-pyridin-2-one ;
N,N-dimethyl-2-{2-methyl-3-[2-oxo-4-(2-thiophen-2-yl-ethoxy)-2H-pyridin-l- ylmethyl] -phenylamino } -acetamide; l-{2-methyl-3-[2-(4-methyl-piperazin-l-yl)-2-oxo-ethylamino]-benzyl}-4-(2- thiophen-2-yl-ethoxy)- 1 H-pyridin-2-one;
l-[2-methyl-3-(2-morpholin-4-yl-2-oxo-ethylamino)-benzyl]-4-(2-thiophen-2-yl- ethoxy)- 1 H-pyridin-2-one;
l-(3-amino-2-methyl-benzyl)-4-(2-furan-2-yl-ethoxy)-lH-pyridin-2-one; l-(3-amino-2-methyl-benzyl)-4-[2-(5-methyl-thiophen-2-yl)-ethoxy]-lH-pyridin-
2-one; l-(3-amino-2-methyl-benzyl)-4-[2-(5-chloro-thiophen-2-yl)-ethoxy]-lH-pyridin- 2-one; l-(2,4-dichloro-benzyl)-4-[2-(3-methyl-thiophen-2-yl)-ethoxy]-lH-pyridin-2- one; l-(3-amino-2-methyl-benzyl)-4-(2-benzo[b]thiophen-3-yl-ethoxy)-lH-pyridin-2- one; l-(3-amino-2-methyl-benzyl)-4-[2-(5-chloro-3-methyl-benzo[b]thiophen-2-yl)- ethoxy] - 1 H-pyridin-2-one ; 1 -(3-amino-2-methyl-benzyl)-4-[2-(3-methyI-benzo[b]thiophen-2-yl)-ethoxy]-
1 H-pyridin-2-one;
1 -(3-amino-2-methyl-benzyl)-4-[2-(5-niethyl-ftιran-2-yl)-ethoxy]- 1 H-pyridin-2- one;
1 -(3 -amino-2-methyl-benzyl)-4- [2-(5-ethyl-ruran-2-yl)-ethoxy] - 1 H-pyridin-2- one;
5-[l -(3-amino-2-methyl-benzyl)-2-oxo- 1 ,2-dihydro-pyridin-4-yloxymethyl]- furan-2-carboxylic acid ethyl ester; l-[3-(2-dimethylamino-ethylamino)-2-methyl-benzyl]-4-(2-thiophen-2-yl- ethoxy)- lH-pyridin-2-one; l-(3-amino-2-methyl-benzyl)-4-[2-(5-methylsulfanyl-thioρhen-2-yl)-ethoxy]-lH- pyridin-2-one; l-(3-amino-2-methyl-benzyl)-4-(2-benzofuran-2-yl-ethoxy)-lH-pyridin-2-one; l-(3-amino-2-methyl-benzyl)-4-[2-(3-methyl-isoxazol-5-yl)-ethoxy]-lH-pyridin- 2-one; l-(3-amino-2-methyl-benzyl)-4-[2-(4,5-dimethyl-thiophen-2-yl)-ethoxy]-lH- pyridin-2-one; l-(3-amino-2-methyl-benzyl)-4-[2-(5-ethyl-thiophen-2-yl)-ethoxy]-lH-pyridin-2- one; l-(3-amino-2,6-dichloro-benzyl)-4-(2-thiophen-2-yl-ethoxy)-lH-pyridin-2-one;
N-{2-methyl-3-[2-oxo-4-(2-thiophen-2-yl-ethoxy)-2H-pyridin-l-ylmethyl]- phenyl } -acetamide; l-[2-methyl-3-(2-piperidin-l-yl-ethylamino)-benzyl]-4-(2-thiophen-2-yl-ethoxy)- 1 H-pyridin-2-one; 1 -[2-methyl-3-(2-morpholin-4-yl-ethylamino)-benzyl]-4-(2-thiophen-2-yl- ethoxy)- 1 H-pyridin-2-one;
N- {2-methyl-3-[2-oxo-4-(2-thioρhen-2-yl-ethoxy)-2H-pyridin- 1 -ylmethyl]- phenyl} -methanesulfonamide; l-(3-amino-2-niethyl-benzyl)-4-[2-(4-bromo-thiophen-2-yl)-ethoxy]-lH-pyridin-
2-one;
1 -(6-chloro-benzo [ 1 ,3]dioxol-5-ylmethyl)-4-(2-pyrrol- 1 -yl-ethoxy)- 1 H-pyridin- 2-one; l-(6-chloro-benzo[l,3]dioxol-5-ylmethyl)-4-(2-thiophen-2-yl-ethoxy)-lH- pyridin-2-one; l-[2-methyl-3-(2-pyrrolidin-l-yl-ethylamino)-benzyl]-4-(2-thiophen-2-yl- ethoxy)- 1 H-pyridin-2-one;
N-(2-{2-methyl-3-[2-oxo-4-(2-thiophen-2-yl-ethoxy)-2H-pyridin-l-ylmethyl]- phenylamino } -ethyl)-acetamide; l-{2-methyl-3-[(pyridin-3-ylmethyl)-amino]-benzyl}-4-(2-thiophen-2-yl- ethoxy)- 1 H-pyridin-2-one;
2-methyl-3-[2-oxo-4-(2-thiophen-2-yl-ethoxy)-2H-pyridin-l-ylmethyl]-phenyl ester; l-{2-methyl-3-[(pyridin-4-ylmethyl)-amino]-benzyl}-4-(2-thioρhen-2-yl- ethoxy)-l H-pyridin-2-one; l-{2-methyl-3-[(thiazol-4-ylmethyl)-amino]-benzyl}-4-(2-thiophen-2-yl-ethoxy)- 1 H-pyridin-2-one;
1 -[3-(4-methoxy-benzyloxy)-2-methyl-benzyl]-4-(2-thiophen-2-yl-ethoxy)- 1 H- pyridin-2-one; l-{3-[(3.5-dimethyl-isoxazol-4-ylmethyl)-amino]-2-methyl-benzyl}-4-(2- thiophen-2-yl-ethoxy)-lH-pyridin-2-one; l-(3-hydroxy-2-methyl-benzyl)-4-(2-thiophen-2-yl-ethoxy)-lH-pyridin-2-one; l-{2-methyl-3-[(l-methyl-pyrrolidin-2-ylmethyl)-amino]-benzyl}-4-(2-thiophen- 2-yl-ethoxy)- 1 H-pyridin-2-one ; l-{2-methyl-3-[2-(l-methyl-pyrrolidin-2-yl)-ethylamino]-benzyl}-4-(2-thiophen-
2-yl-ethoxy)-lH-pyridin-2-one;
(2-{2-methyl-3-[2-oxo-4-(2-thiophen-2-yl-ethoxy)-2H-pyridin-l-ylmethyl]- phenylamino}-ethyl)-phosphonic acid diethyl ester;
4-(isobutylthio)- 1 -(2-methyl-3-nitrobenzyl)pyridine-2(lH)-one; l-(3-amino-2-methylbenzyl)-4-(isobutylthio)pyridine-2(l/f)-one; l-(3-amino-2-methylbenzyl)-4-(furan-2-ylmethylthio)pyridine-2(lH)-one;
1 -(3 -amino-2-methylbenzyl)-4-(pentylthio)pyridine-2-( 1 H)-one; l-(3-amino-2-methylbenzyl)-4-(phenethylthio)pyridine-2(lH)-one; l-(3-amino-2-methylbenzyl)-4-(butylthio)pyridine-2(lH)-one; l-(3-amino-2-methylbenzyl)-4-(thiophen-2-ylmethylthio)pyridine-2(lH)-one; l-(3-amino-2-methylbenzyl)-4-(pentylthio)pyridine-2(lH)-one; l-(3-amino-2-methylbenzyl)-4-(propylthio)pyridine-2(lH)-one;
1 -(3-amino-2-methylbenzyl)-4-( 1 -methylbutylthio)pyridine-2( 1 H)-one; N,N-dimethyl-3-(2-methyl-3-((2-oxo-4-(2-(thiophen-2-yl)ethoxy)pyridin-l(2H)- yl)methyl)phenylamino)propane- 1 -sulfonamide; l-(3-amino-2-methylbenzyl)-4-(2-(thiophene-2-yl)ethylamino)pyridine-2-(lH)- one.
The compound of formula (I) or (II) may be prepared by simple alkylation or arylation using pyridazine derivative, pyrimidinone derivative, triazinone derivative or pyridone derivative.
A preferred example of the compound of formula (I) is a pyridone compound which may be prepared as shown in Reaction Scheme 1 or 2. As used herein, NaH is sodium hydride, TsCl is p-toluenesulfonyl chloride, Ac2O is acetic anhydride, BuOH is butanol, t-BuOH is t-butanol, Pd/C is palladium on carbon, KOtBu is potassium t- butoxide, and Zn is zinc dust. Reaction Scheme 1
Figure imgf000025_0001
Reagents: (a) NaH, benzyloxypropyl bromide, DMF; (b) Pd/C, H2, MeOH; (c) TsCl, TEA, DCM; (d) cyclopropylamine, MeOH Reaction Scheme 2
Figure imgf000025_0002
Reagents: (a) NaH, 2-methyl-3-nitrobenzyl chloride, DMF; (b) hydrazine, Zn, EtOH; (c) Acetic anhydride, TEA, DCM
The pyridone derivatives used as starting materials above may be prepared as shown in Reaction Scheme 3 or 4, respectively. Reaction Scheme 3
Figure imgf000026_0001
Reagents: (a) BnCl, NaH, DMF; (b) PaVC, H2, MeOH
Reaction Scheme 4
Figure imgf000026_0002
Reagents: (a) BuOH, KOtBu, t-BuOH; (b) Ac2O, reflux
Another preferred example of the compound of formula (I) is a pyridone compound being substituted with a methyl group, which may be prepared as shown in Reaction Scheme 5.
Reaction Scheme 5
Figure imgf000026_0003
Reagents: (a) NaH1 pentyl bromide, DMF; (b) benzyl amine, EtOH, reflux Still another preferred example of the compound of formula is a pyridazine compound, which may be prepared as shown in Reaction Scheme 6.
Reaction Scheme 6
Figure imgf000027_0001
Reagents: (a) NaH, pentanol, DMF; (b) 2,4-dichlorobenzyl chloride, NaH, DMF; (c) pd/C, H2, MeOH
Substituting 4-methylpentanol for pentanol in Reaction Scheme 6 will produce 2, (2,4-dichlorobenzyl)-5-4-methylpentyloxy)pyridazin-3(2H)-one:
Figure imgf000027_0002
2-(2,4 -di cMor obenzyl)-5 -(4-€α e&ylp entyl oxy)pyri 4a2in -3(2H) - on e
The compound of formula (I) or (II) effectively inhibits the activity of Fab I.
Accordingly, the present invention provides a method for inhibiting the activity of Fab I, comprising bringing a body fluid such as blood, urine and lymph into contact with the compound of formula (I) or (II).
The present invention also provides a pharmaceutical composition comprising the compound of formula (I) or (II) as an active ingredient in an amount effective to treat or prevent bacteria-related diseases. The inventive pharmaceutical composition may comprise pharmaceutically acceptable carriers, diluents, adjuvants or vehicles. Exemplary carriers, diluents, adjuvants and vehicles include, but are not limited to, ion exchangers, alumina, aluminum stearate, lecithin, serum proteins such as human serum albumin, buffer substances such as phosphates, glycine, sorbic acid, potassium sorbate, partial glyceride mixtures of saturated vegetable fatty acids, water, salts or electrolytes such as protamine sulfate, disodium hydrogen phosphate, potassium hydrogen phosphate, sodium chloride or zinc salts, colloidal silica, magnesium trisilicate, polyvinyl pyrrolidone, cellulose-based substances, polyethylene glycol, sodium carboxy methylcellulose, polyacrylates, waxes, polyethylene-polyoxypropylene-block polymers, polyethylene glycol, wool fat, parabens, chlorobutanol, phenol, sorbic acid, aluminum monostearate, gelatin and the like. It may also be desirable to include isotonic agents, for example sugars, sodium chloride, and the like.
Various formulations of the present invention may be prepared using surfactants such as TWEENs™ or SPANs™, emulsifying agents, extenders, etc., and may be administered orally, sublingualis parenterally, by inhalation spray, topically, rectally, nasally, buccally, vaginally or via an implanted reservoir. The term "parenteral" as used herein includes subcutaneous, intravenous, intramuscular, intra-articular, intra- synovial, intrasternal, intrathecal, intrahepatic, intralesional and intracranial injection or infusion techniques. Preferably, the composition is administered orally, intraperitoneally, subcutaneously, intramuscularly or intravenously.
Sterile injectable formulations may be in the form of aqueous or oleaginous suspensions. These suspensions may be formulated by a conventional method using suitable dispersing or wetting agents and suspending agents such as water, ethanol, polyols (propyleneglycol, polyethyleneglycol, glycerol, and the like), suitable mixtures thereof, vegetable oils (such as olive oil), and injectable organic esters such as ethyl oleate. Proper fluidity can be maintained, for example, by the use of a coating such as lecithin, by the maintenance of the required particle size in the case of dispersions and by the use of surfactants. Formulations suitable for oral administration may be in the form of capsules, tablets, pills, powders, or granules. In such solid dosage forms, the active compound can be admixed with at least one inert carrier such as sodium citrate or dicalcium phosphate; or with fillers, extenders, binders, humectants, disintegrating agents such as calcium carbonate or certain complex silicates, solution retarders such as paraffin, absorption accelerators such as quaternary ammonium compounds, wetting agents such as cetyl alcohol or glycerol monostearate, adsorbents, and lubricants such as magnesium stearate, solid polyethylene glycols, and the like, or mixtures thereof. In the form of capsules, the active compound can be admixed with buffering agents, and can also be admixed with excipients such as lactose or milk sugar as well as high molecular weight polyethyleneglycols, and the like.
Formulations suitable for oral administration may alternatively be in the form of aqueous suspensions, solutions, syrups, etc. When aqueous suspensions are required for oral use, the active ingredient is combined with emulsifying and suspending agents. If desired, certain sweetening, flavoring or coloring agents may also be added. Formulations for oral administration can include a coating, and can be formulated with certain agents so as to release the active compound in a particular portion of the digestive tract.
Formulations for topical administration may be useful in that the target of treatment includes areas or organs readily accessible by topical application, e.g., the eye, the skin or the lower intestinal tract. Topically-transdermal patches may also be used for topical administration.
For topical application to the skin or the lower intestinal tract, the compositions may be formulated in the form of ointments, lotions, creams or sprays form containing the active component suspended or dissolved in one or more suitable carriers. The ointments may contain mineral oil, liquid petrolatum, white petrolatum, propylene glycol, polyoxyethylene, polyoxypropylene, emulsifying wax or water as suitable carriers. The lotions, creams or sprays may contain mineral oil, sorbitan monostearate, polysorbate 60, cetyl esters wax, cetearyl alcohol, 2-octyldodecanol, benzyl alcohol or water as suitable carriers.
For ophthalmic use, the compositions may be formulated as micronized suspensions or solutions in isotonic, pH adjusted sterile saline, either with or without a preservative such as benzylalkonium chloride. Alternatively, the compositions may be formulated in ophthalmic ointments such as petrolatum. Formulations suitable for administration by nasal aerosol or inhalation may be in the form of solutions in saline. The solutions may contain benzyl alcohol or other suitable preservatives, absorption promoters to enhance bioavailability, fluorocarbons, and/or other conventional solubilizing or dispersing agents.
Formulations suitable for rectal or vaginal administration can be prepared by mixing the compounds of the present invention with suitable non-irritating excipients or carriers such as a suppository wax, cocoa butter, or polyethyleneglycol which melt at body temperature.
If necessary, the inventive compound may be used with other antimicrobials such as penicillin or cephalosporin.
A single dose of the compound of formula (I) or (II) may range from about 50 to 1,500 mg, although the dose may be varied depending upon the age, body weight and symptoms of the patient. A typical daily dose of the compound of formula (I) or (II) may range from about 50 to 5,000 mg, or from about 150 to 3,000 mg for adults, and can be from about 50 to 2000 mg, or from about 100 to 2000 mg, or from about 300 to 2500 mg, or from about 500 to 4000 mg, or from about 500 to 5000 mg.
Further, the present invention provides a method for treating bacteria-related diseases, comprising administering an effective amount of a compound of formula (I) or (II) to a patient in need of such treatment. The patient to be treated by the above method may include a human or non-human mammalian.
The present invention will be described in further detail with reference to Examples. However, it should be understood that the present invention is not restricted by the specific Examples.
Preparation Example 1: Synthesis of 4-pentyloxy-lH-pyridin-2-one
A solution of pentanol(2.7g, 31mmol) and tert-butoxide(3.5g, 31mmol) in solvent of tert-butanol was stirred for lhr at room temperature followed by addition of 4-nitropyridine-N-oxide(4g, 28.6mmol). After the reaction was done, the resulting solution was worked up with ethyl acetate and water, separated and the organic solvent was dried completely. After the addition of toluene, the solvent was removed under a reduced pressure. Acetic anhydride(40ml) was added to the residual mixture and refluxed for 3hrs. Acetic anhydride was dried completely followed by adding of
MeOH(20ml) and 3N NaOH(5ml) and stirring lhr. MeOH was dried adequately then the residual mixture was made neutral with 6N HCl. The resulting solution was extracted with Ethyl acetate(80ml) and subjected to silica gel column chromatography(ethyl acetate/MeOH, 10:1) to obtain the titled compound(2.3g, 56%).
1H NMR (CDCl3, 300 MHz) δ 0.93 (t, 3H), 1.33-1.44 (m, 4H), 1.72-1.79 (m, 2H), 3.91
(t, 2H), 5.91-6.08 (m, 2H), 7.40 (d, IH)
Example 1: 4-benzyloxy-l-(2-chloro-benzyl)-lH-pyridin-2-one
A solution of 4~benzyloxy-lH-pyridone(300mg, 1.49mmol) and NaH(60mg,
1.49mmol) in solvent of DMF was stirred for 30min followed by adding 2-chlorobenzyl chloride(240mg, 1.49mmol) further stirring for 30min at room temperature. The resulting solution was worked up with Water and dichloromethane and purified by column chromatography(ethyl acetate/hexane, 1:1) to obtain the titled compound(320mg, 67%).
1H NMR (CDCl3, 300 MHz) δ 5.00 (s, 2H), 5.20 (s, 2H), 5.97 (dd, IH), 6.04 (d, IH),
7.17-7.39 (m, 10H)
Examples 2 to 13: The procedure of Example 1 was repeated except the starting material to obtain the titled compound.
Example 2: 4-benzyloxy-l~(4-chloro-benzyl)-lH-pyridin-2-one 1H NMR (CDCl3, 300 MHz) δ 4.96 (s, 2H)5 5.01 (s, 2H), 5.93 (dd, IH)5 5.99 (d, IH)5 7.09 (d, IH)5 7.19 (d, 2H)5 7.24 (d, 2H)5 7.28-7.36 (m, 5H)
Example 3: 4-benzyloxy-l-(4-nitro-benzyl)-lH-pyridin-2-one 1B. NMR (CDCl35 300 MHz) δ 5.08 (s, 2H), 5.47 (s, 2H), 6.39-6.60 (m, 2H), 7.35-7.59 (m, 7H)5 7.95 (d, IH), 8.18-8.23 (m, 2H)
Example 4: 4-benzyloxy-l-(2,5-dichloro-benzyl)-lH-pyridin-2-one
1H NMR (CDCl3, 300 MHz) δ 4.98 (s, 2H)5 5.12 (s, 2H)5 5.96-6.03 (m, 2H)5 7.14-7.39 (m, 9H)
Example 5: 4-benzyloxy-l-(2,4-dichloro-benzyl)-lH-pyridin-2-one
1H NMR (CDCl3, 300 MHz) δ 5.00 (s, 2H), 5.14 (s, 2H), 5.97-6.03 (m, 2H)5 7.18-7.41 (m, 9H)
Example 6: 4-benzyloxy-2-(4-methoxy-benzyloxy)-pyridine
1H NMR (CDCl35 300 MHz) δ 3.80 (s, 3H)5 5.05 (s, 2H), 5.28 (s, 2H), 6.31 (d, IH), 6.55 (dd, IH), 6.90 (d, IH), 7.29-7.40 (m, 7H)5 7.99 (d, IH)
Example 7: 4-benzyloxy-l-(4-methoxy-benzyl)-lH-pyridin-2-one
1H NMR (CDCl3, 300 MHz) δ 3.79 (s, 3H)5 4.98 (s, 2H), 5.01 (s, 2H), 5.92 (dd, IH), 6.01 (d, IH), 6.86 (d, 2H), 7.11 (d, IH)5 7.22-7.26 (m, 3H)5 7.34-7.38 (m, 4H)
Example 8: 4-benzyloxy-2-(4-methyl-benzyloxy)-pyridine 1H NMR (CDCl3, 300 MHz) δ 2.37 (s, 3H), 5.06 (s, 2H), 5.33 (s, 2H), 6.34 (d, IH), 6.56 (dd, IH), 7.19 (d, 2H), 7.34-7.41 (m, 7H), 8.00 (d, IH)
Example 9: 4-benzyloxy-l-(4-methyl-benzyl)-lH-pyridin-2-one 1H NMR (CDCl3, 300 MHz) δ 2.33 (s, 3H), 4.98 (s, 2H), 5.04 (s, 2H), 5.93 (dd, IH), 6.02 (d, IH), 7.10-7.19 (m, 5H), 7.34-7.38 (m, 5H)
Example 10: 4-benzyloxy-l-(6-chloro-pyridm-3-ylmethyl)-lH-pyridm-2-one
1H NMR (CDCl3, 300 MHz) δ 4.99 (s, 2H), 5.04 (s, 2H), 6.00-6.02 (m, 2H), 7.15-7.38 (m, 7H), 7.66 (dd, IH), 8.34-8.37 (m, IH)
Example 11: 4-benzyloxy-l-(3-chloro-benzyl)-lH-pyridin-2-one
1H NMR (CDCl3, 300 MHz) δ 4.96 (s, 2H), 5.01 (s, 2H), 5.94 (dd, IH), 6.00 (d, IH), 7.09-7.36 (m, 10H)
Example 12: l-benzyl-4-benzyloxy-lH-pyridin-2-one
1U NMR (CDCl3, 300 MHz) δ 4.96 (s, 2H), 5.06 (s, 2H), 5.92 (dd, IH), 6.01 (d, IH), 7.10 (d, IH), 7.24-7.36 (m, 10H)
Example 13: l-(4-amino-benzyl)-4-benzyloxy-lH-pyridin-2-one
1H NMR (CDCl3, 300 MHz) δ 3.73 (br s, 2H), 4.95 (s, 2H), 4.97 (s, 2H), 5.90 (dd, IH), 6.00 (d, IH), 6.63 (d, 2H), 7.08-7.37 (m, 8H) Example 14: l-(2,4-dichIoro-benzyl)-4-hydroxy-lH-pyridin-2-one
4-benzyloxy-l-(2,4-dichloro-benzyl)-lH-pyridin-2-one synthesized by the same method as Example 1 was hydrogenated with Pd/C to obtain the titled compound. 1U NMR (CD3OD5 300 MHz) δ 5.17 (s, 2H)5 5.86 (d, IH), 6.10 (dd, IH), 6.99 (d, IH)5 7.27-7.32 (m, IH), 7.50-7.52 (m, 2H)
Example 15: 3-benzyl-l-(2,4-dichloro-benzyl)-4-hydroxy-lH-pyridin-2-one l-(2,4-dichloro-benzyl)-4-hydroxy-lH-pyridin-2-one synthesized in Example 14 was dissolved in DMF followed by adding NaH and benzyl bromide to obtain 4- benzyloxy-l-(2,4-dichloro-benzyl)-lH-pyridin-2-one and the titled compound in the ratio of 1 : 1.
1H NMR (CDCl3, 300 MHz) δ 4.00 (s, 2H)5 5.13 (s, 2H), 5.87 (d, IH), 7.25-7.33 (m, 9H)
Examples 16 to 225: The procedure of Example 1 was repeated except the starting material to obtain the titled compound.
Example 16: 4-(biphenyl-4-ylmethoxy)- 1 -(2,4-dichloro-benzyl)- 1 H-pyridin-2-one 1H NMR (CDCI3, 300 MHz) δ 5.04 (s, 2H), 5.15 (s, 2H), 6.01 (dd, IH), 6.06 (d, IH)5 7.22-7.63 (m, 13H)
Example 17: 1 -(2,4-dichloro-benzyl)-4-(2,4-dichloro-benzyloxy)-lH-pyridin-2-one 1H NMR (CDCl3, 300 MHz) δ 5.06 (s, 2H), 5.15 (s, 2H), 5.99-6.01 (m, 2H), 7.15-7.44 (m, 7H) Example 18: 4-(2-chloro-benzyloxy)- 1 -(2,4-dichloro-benzyl)- 1 H-pyridin-2-one 1H NMR (CDCl3, 300 MHz) δ 5.11 (s, 2H)5 5.16 (s, 2H)5 6.00-6.04 (m, 2H)5 7.21-7.47 (m, 8H)
Example 19: l-(2,4-dichloro-benzyl)-4-methoxy-l H-pyridin-2-one
1H NMR (CDCl3, 300 MHz) δ 3.78 (s, 3H)5 5.14 (s, 2H), 5.91-5.94 (m, 2H)5 7.16-7.22
(m, 3H), 7.41 (s, IH)
Example 20: l-(2,4-dichloro-benzyl)-4-isopropoxy-l H-pyridin-2-one
1H NMR (CDCl3, 300 MHz) δ 1.34 (d, 6H)5 4.47-4.55 (m, IH)5 5.86-5.91 (m, 2H)5 7.15- 7.21 (m, 3H), 7.41 (s, IH)
Example 21 : 4-cyclohexylmethoxy- 1 -(2,4-dichloro-benzyl)- 1 H-pyridin-2-one 1H NMR (CDCl3, 300 MHz) δ 0.86-1.83 (m, HH), 3.71 (d, 2H), 5.14 (s, 2H), 5.90-5.94 (m, 2H)5 7.15-7.23 (m, 3H), 7.40 (s, IH)
Example 22: 3-(2-chloro-benzyl)-4-hydroxy-l H-pyridin-2-one 1H NMR (CD3OD5 300 MHz) δ 3.82 (s, 2H), 6.12 (d, IH)5 7.06-7.28 (m, 5H)
Example 23: l-(254-dichloro-benzyl)-4-propoxy-l H-pyridin-2-one
1H NMR (CDCl3, 300 MHz) δ 1.02 (t, 3H)5 1.74-1.85 (m, 2H), 3.88 (t, 2H), 5.14 (s, 2H),
5.91-5.94 (m, 2H), 7.15-7.24 (m, 3H)5 7.40 (s, IH) Example 24: 1 -(2,4-dichloro-benzyl)-4-isobutoxy- 1 H-pyridin-2-one
1U NMR (CDCl3, 300 MHz) δ 1.00 (d, 6H), 2.03-2.12 (m, IH), 3.68 (d, 2H), 5.14 (s,
2H), 5.90-5.95 (m, 2H), 7.15-7.23 (m, 3H), 7.41 (s, IH)
Example 25: 4-butoxy-l-(2,4-dichloro-benzyl)-l H-pyridin-2-one
1H NMR (CDCl3, 300 MHz) δ 0.97 (t, 3H), 1.40-1.52 (m, 2H), 1.71-1.80 (m, 2H), 3.92 (t, 2H), 5.14 (s, 2H), 5.90-5.92 (m, 2H), 7.15-7.23 (m, 3H), 7.41 (s, IH)
Example 26: l-(2,4-dichloro-benzyl)-4-octyloxy-l H-pyridin-2-one 1H NMR (CDCl3, 300 MHz) δ 0.84 (t, 3H), 1.24-1.52 (m, 10H), 1.67-1.76 (m, 2H), 3.86 (t, 2H), 5.09 (s, 2H), 5.86-5.89 (m, 2H), 7.10-7.18 (m, 3H), 7.36 (s, IH)
Example 27: 1 -(2,4-dichloro-benzyl)-4-(4-methyl-pentoxy)-l H-pyridin-2-one 1H NMR (CDCl3, 300 MHz) δ 0.86 (d, 6H), 1.24-1.29 (m, 2H), 1.50-1.59 (m, IH), 1.67- 1.77 (m, 2H), 3.86 (t, 2H), 5.10 (s, 2H), 5.87-5.90 (m, 2H), 7.11-7.16 (m, 3H), 7.36 (s, IH)
Example 28: 4-(but-3-enyIoxy)-l-(2,4-dichloro-benzyl)-lH-pyridin-2-one 1H NMR (CDCl3, 300 MHz) δ 2.48 (q, 2H), 3.93 (t, 2H), 5.06-5.15 (m, 4H), 5.76-5.89 (m, 3H), 7.11-7.15 (m, 3H), 7.36 (s, IH)
Example 29: l-(2,4-dichloro-benzyl)-l H-pyridin-2-one
1H NMR (CDCl3, 300 MHz) δ 1.78-1.87 (m, 2H), 2.16 (q, 2H), 3.89 (t, 2H), 4.95-5.09
(m, 4H), 5.71-5.88 (m, 3H), 7.11-7.15 (m, 3H), 7.36 (s, IH) Example 30: 1 -(2,4-dichloro-benzyl)-4-pentyloxy- 1 H-pyridin-2-one 1H NMR (CDCl3, 300 MHz) δ 0.93 (t, 3H), 1.33-1.44 (m, 4H), 1.72-1.79 (m, 2H)5 3.91 (t, 2H), 5.14 (s, 2H), 7.16-7.22 (m, 3H), 7.40 (d, IH)
Example 31: [l-(2,4-dichloro-benzyl)-2-oxo-l,2-dihydro-pyridin-4-yloxy] -acetic acid ethylester
1H NMR (CDCl3, 300 MHz) δ 3.77 (s, 3H)5 4.54 (s, 2H), 5.09 (s, 2H), 5.77 (d, IH), 5.99 (dd, IH), 7.17-7.22 (m, 3H)5 7.37 (s, IH)
Example 32: l-(2,4-dichloro-benzyl)-4-(3-methyl-butoxy)-lH-pyridin-2-one
1H NMR (CDCl35 300 MHz) δ 0.87 (d, 6H), 1.54-1.76 (m, 3H), 3.86 (t, 2H), 5.00 (s,
2H), 5.79 (dd, IH), 5.86 (d, IH)5 7.04 (d, IH), 7.13-7.27 (m, 3H)
Example 33 : 1 -benzyl-4-pentyloxy- 1 H-pyridin-2-one
1H NMR (CDCl3, 300 MHz) δ 0.93 (t, 3H), 1.32-1.40 (m, 4H), 1.75-1.79 (m, 2H), 3.92 (t, 2H)5 5.10 (s, 2H)5 5.87-5.93 (m, 2H), 7.11 (d, IH)5 7.25-7.32 (m, 5H)
Example 34: l-(2-chloro-benzyl)-4-pentyloxy-l H-pyridin-2-one 1U NMR (CDCl3, 300 MHz) δ 0.92 (t, 3H)5 1.31-1.42 (m, 4H), 1.72-1.79 (m, 2H), 3.91 (t, 2H), 5.19 (S, 2H), 5.89-5.92 (m, 2H)5 7.14-7.26 (m, 4H), 7.37-7.40 (m, IH)
Example 35: 4-pentyloxy-l -propyl- lH-pyridin-2-one
1H NMR (CDCl3, 300 MHz) δ 0.90-0.96 (m, 6H), 1.28-1.38 (m, 4H), 1.67-1.80 (m, 4H), 3.82 (t, 2H), 3.89 (t, 2H), 5.87 (d, 2H), 7.07-7.10 (m, IH)
Example 36: l-butyl-4-pentyloxy~lH-pyridin-2-one
1H NMR (CDCl3, 300 MHz) δ 0.89-0.96 (m, 6H), 1.29-1.42 (m, 6H), 1.64-1.78 (m, 4H), 3.83-3.91 (m, 4H), 5.86-5.88 (m, 2H), 7.07-7.10 (m, IH)
Example 37: l-isobutyl-4-pentyloxy-lH-pyridin-2-one
1H NMR (CDCl3, 300 MHz) δ 0.91-0.93 (m, 9H), 1.33-1.39 (m, 4H), 1.71-1.78 (m, 2H), 2.10-2.19 (m, IH), 3.65 (d, 2H), 3.89 (t, 2H), 5.84-5.87 (m, 2H), 7.05 (d, IH)
Example 38: l-(3-methyl-butyl)-4-pentyloxy-lH-pyridin-2-one
1H NMR (CDCl3, 300 MHz) δ 0.90-0.96 (m, 9H), 1.33-1.39 (m, 4H), 1.55-1.78 (m, 5H),
3.84-3.91 (m, 4H), 5.86-5.88 (m, 2H), 7.07-7.10 (m, IH)
Example 39: l-(2,4-dichloro-benzyl)-4-hexyloxy-lH-pyridin-2-one
1H NMR (CDCl3, 300 MHz) δ 0.90 (t, 3H), 1.25-1.34 (m, 4H), 1.71-1.80 (m, 2H), 3.91 (t, 2H), 5.14 (s, 2H), 5.91-5.93 (m, 2H), 7.14-7.23 (m, 3H), 7.40 (s, IH)
Example 40: l-(2,4-dichloro-benzyl)-4-heptoxy-lH-pyridin-2-one 1H NMR (CDCl3, 300 MHz) δ 0.75 (t, 3H), 1.09-1.54 (m, 8H), 1.71-1.80 (m, 2H), 3.91 (t, 2H), 5.13 (s, 2H), 5.86-5.92 (m, 2H), 7.14-7.22 (m, 3H), 7.40 (s, IH)
Example 41: l-(4-chloro-benzyl)-4-pentyloxy-lH-pyridin-2-one
1H NMR (CDCl3, 300 MHz) δ 0.92 (t, 3H), 1.33-1.42 (m, 4H), 1.71-1.80 (m, 2H), 3.90 (t, 2H), 5.04 (s, 2H), 5.87-5.91 (m, 2H)5 7.08 (d, IH)5 7.20 (d, 2H)5 7.30 (d, 2H)
Example 42: 4-aryloxy-l-(2,4-dichloro-benzyl)-lH-pyridin-2-one 1H NMR (CDCl35 300 MHz) δ 4.48 (d, 2H)5 5.14 (s, 2H), 5.32-5.45 (m, 2H), 5.94-6.07 (m, 3H)5 7.18-7.20 (m, 3H), 7.41 (s, IH)
Example 43: 1 -(2,4-dichloro-benzyl)-4-(3-methoxy-propoxy)-lH-pyridin-2-one 1H NMR (CDCl35 300 MHz) δ 2.01-2.07 (m, 2H)5 3.35 (s, 3H)5 3.52 (t, 2H), 4.02 (t, 2H)5 5.14 (s, 2H)5 5.91-5.94 (m, 2H), 7.16-7.20 (m, 3H)5 7.41 (s, IH)
Example 44: l-(2,4-dichloro-benzyl)-4-(3-ethylamino-propoxy)-lH-pyridin-2-one
1H NMR (CDCl3, 300 MHz) δ 1.25-1.52 (m, 5H)5 2.92-3.05 (m, 4H)5 4.03 (t, 2H)5 5.13
(s, 2H), 5.91-5.93 (m, 2H), 7.17-7.19 (m, 3H), 7.41 (s, IH)5 8.48 (br s, IH)
Example 45 : 1 -(2,4-dichloro-benzyl)-4-(2-ethoxy-ethoxy) - 1 H-pyridin-2-one
1H NMR (CDCl3, 300 MHz) δ 1.25 (t, 3H)5 3.58 (q, 2H)5 3.77 (t, 2H)5 4.08 (t, 2H)5 5.14 (s, 2H), 5.92 (d, IH), 5.99 (dd, IH), 7.16-7.23 (m, 3H)5 7.41 (s, IH)
Example 46: l-(3-methyl-but-2-enyl)-4-pentyloxy-l H-pyridin-2-one 1H NMR (CDCl3, 300 MHz) δ 0.92 (t, 3H)5 1.33-1.38 (m, 4H)5 1.71-1.73 (m, 2H), 1.76 (s, 6H)5 3.89 (t, 2H)5 4.47 (d, 2H), 5.27 (t, IH)5 5.87-5.88 (m, 2H)5 7.10-7.13 (m, IH)
Example 47: 5-(2-oxo-4-pentyloxy-2H-pyridin-l-ylmethyl)-furan-2-carboxyl acid ethylester 1H NMR (CDCl3, 300 MHz) δ 0.92 (t, 3H), 1.33-1.44 (m, 7H), 1.73-1.80 (m, 2H), 3.89 (t, 2H), 4.34 (q, 2H), 5.09 (s, 2H), 5.86 (d, IH), 5.92 (dd, IH), 6.47 (d, IH), 7.09 (d, IH), 7.29 (d, IH)
Example 48: 5-(2-oxo-4-pentyloxy-2H-pyridin-l-ylmethyl)-furan-2-carboxyl acid
1H NMR (CD3OD, 300 MHz) δ 0.94 (t, 3H), 1.37-1.45 (m, 4H), 1.73-1.80 (m, 2H), 3.97 (t, 2H), 5.13 (s, 2H), 5.89 (d, IH), 6.11 (dd, IH), 6.41 (d, IH)3 6.93 (d, IH), 7.65 (d, IH)
Example 49: 4-pentyloxy-l-thiazol-4-ylmethyl-lH-pyridin-2-one 1H NMR (CDCl3, 300 MHz) δ 0.92 (t, 3H), 1.32-1.44 (m, 4H), 1.70-1.80 (m, 2H), 3.89 (t, 2H), 5.22 (s, 2H), 5.88 (d, IH), 5.92 (dd, IH), 7.38-7.42 (m, 2H), 8.76 (s, IH)
Example 50: 4-pentyloxy-l-pyridin~3-ylmethyl-lH-pyridin-2-one 1H NMR (CDCl3, 300 MHz) δ 0.93 (t, 3H), 1.32-1.45 (m, 4H), 1.74-1.83 (m, 2H), 3.96 (t, 2H), 5.55 (s, 2H), 6.29 (d, IH), 6.50 (dd, IH)5 7.40 (s, IH), 7.96 (d, IH)5 8.84 (d, IH)
Example 51: l-(2,4-dichloro-benzyl)-4-(4-methyl-pent-3-enyloxy)-lH-pyridin-2-one 1H NMR (CDCl3, 300 MHz) δ 1.65 (s, 3H), 1.73 (s, 3H), 2.46 (q, 2H), 3.89 (t, 2H)5 5.14 (s5 2H)5 5.91-5.94 (m, 2H), 7.15-7.13 (m, 3H), 7.27 (s, IH)5 7.41 (s, IH)
Example 52: l-(2,4-dichloro-benzyl)-4-(3-methoxy-propoxy)-lH-pyridin-2-one 1H NMR (CDCl3, 300 MHz) δ 0.88 (d, 6H)5 1.18-1.26 (m, 4H), 1.37-1.77 (m, 5H)5 3.92 (t, 2H)5 5.14 (s, 2H), 5.91-5.93 (m, 2H)5 7.15-7.23 (m, 3H)5 7.41 (s, IH) Example 53 : 1 -(2,4-dichloro-benzyl)-4-phenetyloxy- 1 H-pyridin-2-one
1H NMR (CDCl3, 300 MHz) δ 3.09 (t, 2H), 4.15 (t, 2H)5 5.14 (s, 2H), 5.91-5.99 (m, 2H),
7.16-7.40 (m, 9H)
Example 54: l-(2-methyl-benzyl)-4-pentyloxy-l H-pyridin-2-one
1U NMR (CDCl3, 300 MHz) δ 0.93 (t, 3H), 1.33-1.43 (m, 4H), 1.75-1.79 (m, 2H), 2.28 (s, 3H), 3.92 (t, 2H), 5.08 (s, 2H), 5.86 (dd, IH)5 5.94 (d, IH)5 6.93 (d, IH)5 7.03 (d, IH)5 7.15-7.23 (m, 3H)
Example 55: 4-pentyl-l-phenetyl-l H-pyridin-2-one
1H NMR (CDCl3, 300 MHz) δ 0.86 (t, 3H), 1.27-1.33 (m, 4H), 1.65-1.72 (m, 2H), 2.96 (t, 2H), 3.83 (t, 2H), 4.01 (t, 2H), 5.65 (dd, IH)5 5.83 (d, IH), 6.65 (d, IH), 7.08 (d, IH)5 7.13-7.25 (m, 3H)
Example 56: l-(2,4-dichloro-5-fluoro-benzyl)-4-pentyloxy-l H-pyridin-2-one
1H NMR (CDCl3, 300 MHz) δ 0.93 (t, 3H)5 1.31-1.43 (m, 4H)5 1.73-1.80 (m, 2H), 3.92 (t, 2H), 5.10 (s, 2H), 5.92-5.96 (m, 2H)5 7.02 (d, IH), 7.16 (d, IH)5 7.44 (d, IH)
Example 57 : 1 -(3 ,4-dichloro-benzyl)-4-pentyloxy- 1 H-pyridin-2-one 1H NMR (CDCI3, 300 MHz) δ 0.93 (t, 3H)5 1.31-1.46 (m, 4H), 1.73-1.82 (m, 2H)5 3.92 (t, 2H)5 5.02 (s, 2H)5 5.92-5.95 (m, 2H)5 7.10-7.15 (m, 2H)5 7.36-7.42 (m, 2H)
Example 58: 1 -(3 ,4-difluoro-benzyl)-4-pentyloxy-l H-pyridin-2-one
1H NMR (CDCl3, 300 MHz) δ 0.93 (t, 3H)5 1.32-1.43 (m, 4H)5 1.73-1.80 (m, 2H)5 3.92 (t, 2H), 5.02 (s, 2H), 5.91-5.94 (m, 2H), 7.03-7.17 (m, 4H)
Example 59: 4-(4-benzyloxy-butoxy)-l-(2,4-dichloro-benzyl)-lH-pyridin-2-one 1H NMR (CDCl3, 300 MHz) δ 1.68-1.94 (m. 4H), 3.54 (t, 2H)5 3.96 (t, 2H)5 4.53 (s, 2H), 5.15 (s, 2H), 5.90-5.93 (m, 2H), 7.16-7.42 (m, 9H)
Example 60: 1 -(2,4-dichloro-benzyl)-4-(4-hydroxy-butoxy)-lH-pyridin-2-one 1H NMR (CDCl3, 300 MHz) δ 1.70-1.91 (m, 4H), 3.72 (t, 2H), 3.98 (t, 2H), 5.14 (s, 2H), 5.92-5.94 (m, 2H), 7.16-7.25 (m, 3H)5 7.41 (s, IH)
Example 61: 4-(5-benzyloxy-pentyloxy)-l-(2,4-dichloro-benzyl)-lH-pyridin-2-one
1H NMR (CDCl35 300 MHz) δ 1.52-1.85 (m, 6H), 3.51 (t, 2H), 3.94 (t, 2H), 4.53 (s, 2H),
5.15 (s, 2H), 5.90-5.94 (m, 2H), 7.16-7.42 (m, 9H)
Example 62: l-(2,4-dichloro-benzyl)-4-(5-hydroxy-pentyloxy)-lH-pyridin-2-one
1H NMR (CDCl3, 300 MHz) δ 1.44-1.83 (m, 6H), 3.70 (t, 2H), 3.93 (t, 2H), 5.14 (s, 2H), 5.91-5.92 (m, 2H), 7.15-7.20 (m, 3H), 7.41 (s, IH)
Example 63: l-(6-chloro-benzo[l,3]dioxol-5-ylmethyl)-4-pentyloxy-lH-pyridin-2-one 1H NMR (CDCl3, 300 MHz) δ 0.93 (t, 3H), 1.35-1.43 (m, 4H), 1.74-1.79 (m, 2H), 3.91 (t, 2H), 5.10 (s, 2H), 5.88-5.91 (m, 2H), 5.96 (s, 2H), 6.81 (s, IH), 6.84 (s, IH), 7.18 (dd, IH)
Example 64: l-(2,4-dichloro-benzyl)-4-(2-m ethyl -benzyloxy)-lH-pyridin-2-one 1H NMR (CDCl3, 300 MHz) δ 2.35 (s, 3H)5 4.99 (s, 2H), 5.16 (s, 2H)5 5.98 (dd5 IH), 6.08 (d, IH), 7.20-7.42 (m, 8H)
Example 65: l-(2,4-dichloro-benzyl)-4-(4-methyl-benzyloxy)-lH-pyridin-2-one 1H NMR (CDCl3, 300 MHz) δ 2.37 (s, 3H)5 4.95 (s, 2H), 5.15 (s, 2H)5 5.98 (dd, IH), 6.03 (d, IH)5 7.18-7.30 (m, 8H)
Example 66: l-(2-nitro-benzyl)-4-pentyloxy-lH-pyridin-2-one 1H NMR (CDCl3, 300 MHz) δ 0.93 (t, 3H), 1.34-1.43 (m, 4H)5 1.73-1.82 (m, 2H), 3.93 (t, 2H), 5.46 (s, 2H)5 5.93 (d, IH), 5.98 (dd, IH), 7.10 (d, IH), 7.17 (d, IH)5 7.44 (t, IH), 7.56 (t, IH), 8.10 (d, IH)
Example 67: l-(2-amino-benzyl)-4-pentyloxy-lH-pyridin-2-one 1H NMR (CDCl3, 300 MHz) δ 0.91 (t, 3H)5 1.30-1.39 (m, 4H), 1.69-1.76 (m, 2H)5 3.89 (t, 2H), 4.75 (br s, 2H)5 5.00 (s, 2H)5 5.89-5.93 (m, 2H)5 6.62-6.70 (m, 2H), 7.09-7.23 (m, 3H)
Example 68: N-[2-(2-oxo-4-pentyloxy-2H-pyridin-l-ylmethyl)-phenyl]-acetamide 1H NMR (CDCl3, 300 MHz) δ 0.92 (t, 3H)5 1.26-1.38 (m, 4H)5 1.74-1.78 (m, 2H), 2.29 (s, 3H), 3.91 (t, 2H), 5.01 (s, 2H), 5.94 (d, IH), 6.01 (dd, IH)5 7.08 (t, IH), 7.31-7.38 (m, 3H), 8.20 (d, IH), 10.56 (br s, IH)
Example 69: 4-pentyloxy-l-(2-trifluoromethyl -benzyl)- lH-pyridin-2-one
1H NMR (CDCl3, 300 MHz) δ 0.94 (t, 3H), 1.31-1.42 (m, 4H), 1.75-1.81 (m, 2H)5 3.95 (t, 2H)5 5.32 (s, 2H), 5.93 (dd5 IH)5 5.98 (d, IH), 7.04 (d, IH)5 7.15 (d, IH)5 7.38 (t, IH)5 7.49 (t, IH)5 7.69 (d, IH)
Example 70: N-[4-(4-benzyloxy-2-oxo-2H-pyridin-l -ylmethyl)-phenyl]acetamide 1H NMR (CDCl3, 300 MHz) δ 2.18 (s, 3H)5 4.99 (s, 2H), 5.04 (s, 2H), 5.98 (dd, IH)5 6.02 (d, IH)5 7.14-7.46 (m, 10H)5 7.82 (br s, IH)
Example 71: l-(2,4-dichloro-benzyl)-4-(naphthalen-2-ylmethoxy)-lH-pyridin-2-one 1H NMR (CDCl3, 300 MHz) δ 5.15 (s, 2H), 5.16 (s, 2H)5 5.99-6.09 (m, 2H), 7.18-7.55 (m, 7H)5 7.83-7.90 (m, 4H)
Example 72: 1 -naphthalen^-ylmethyM-pentyloxy-lH-pyridin^-one 1B NMR (CDCl3, 300 MHz) δ 0.92 (t, 3H)5 1.35-1.43 (m, 4H)5 1.73-1.76 (m, 2H), 3.91 (t, 2H)5 5.24 (s, 2H), 5.84-5.96 (m, 2H)5 7.13 (d, IH), 7.26-7.49 (m, 3H), 7.70 (s, IH), 7.79-7.83 (m, 3H)
Example 73 : 4-benzyloxy- 1 -(6-chloro-benzo[ 1 ,3]dioxol-5-ylmethyl)- 1 H-pyridin-2-one 1H NMR (CDCl3, 300 MHz) δ 4.99 (s, 2H), 5.10 (s, 2H), 5.94-6.03 (m, 4H), 6.84 (d, 2H)5 7.20 (d, IH), 7.33-7.39 (m, 5H)
Example 74: l-(6-chloro-benzo[l,3]dioxol-5-ylmethyl)-4-(3-methyl-butoxy)-lH- pyridin-2-one
1H NMR (CDCl3, 300 MHz) δ 0.92 (d, 6H)5 1.58-1.66 (m, 3H), 3.92 (t, 2H)5 5.07 (s,
2H), 5.86 (dd, IH), 5.90 (d, IH)5 5.93 (s, 2H), 6.80 (d, 2H), 7.14 (d, IH) Example 75: 1 -(2-methyl-benzyl)-4-(3-methyl-butoxy)- 1 H-pyridin-2-one 1H NMR (CDCl3, 300 MHz) δ 0.92 (d, 6H), 1.63 (q, 2H), 1.72-1.81 (m, IH), 3.93 (t, 2H)5 5.05 (s, 2H), 5.82 (dd, IH), 5.92 (d, IH), 6.90 (d, IH), 7.01 (d, IH)5 7.13-7.20 (m, 3H)
Example 76: 4-(3-methyl-butoxy)-l-(2-nitro-benzyl)-lH-pyridin-2-one 1H NMR (CDCl3, 300 MHz) δ 0.93 (d, 6H), 1.65 (q, 2H), 1.69-1.78 (m, IH), 3.95 (t, 2H), 5.45 (s, 2H), 5.93-5.96 (m, 2H), 7.11 (d, IH), 7.14 (d, IH), 7.44 (t, IH), 7.53 (t, IH), 8.08 (d, IH)
Example 77: l-(2,4-dichloro-beiizyl)-4-pentylamino-l H-pyridin-2-one 1H NMR (CDCl3, 300 MHz) δ 0.88 (t, 3H), 1.24-1.34 (m, 4H), 1.57-1.84 (m, 2H), 3.19 (br s, IH), 3.47 (q, 2H), 5.03 (s, 2H)5 5.56 (d, IH), 7.15-7.38 (m, 4H)
Example 78: l-(2,3-dichloro-benzyl)-4-pentyloxy-lH-pyridin-2-one
1H NMR (CDCl3, 300 MHz) δ 0.90 (t, 3H), 1.28-1.40 (m, 4H),.1.70-1.77 (m, 2H), 3.89
(t, 2H), 5.17 (s, 2H), 5.89-5.92 (m, 2H), 7.01 (d, IH), 7.11-7.16 (m, 2H), 7.37 (d, IH)
Example 79: l-(2-methoxy-benzyl)-4-pentyloxy-l H-pyridin-2-one
1H NMR (CDCl3, 300 MHz) δ 0.90 (t, 3H), 1.27-1.36 (m, 4H), 1.68-1.77 (m, 2H), 3.83 (s, 3H), 3.87 (t, 2H), 5.05 (s, 2H), 5.81 (dd, IH), 5.86 (d, IH), 6.84-6.92 (m, 2H)5 7.18- 7.27 (m, 3H) Example 80: l-(253-dimethoxy-benzyl)-4-pentyloxy-lH~pyridin-2-one 1H iNMR (CDCl35 300 MHz) δ 0.89 (t, 3H)5 1.29-1.38 (m, 4H)5 1.67-1.74 (m, 2H)5 3.81- 3.88 (m, 8H), 5.08 (s, 2H)5 5.80 (dd5 IH)5 5.86 (d, IH)5 6.82-6.87 (m, 2H), 6.98 (t, IH), 7.18 (d, IH)
Example 81: 4-(5-benzyloxy-pentyloxy)-l-(6-chloro-benzo[l,3]dioxol-5-ylmethyl) - lH-pyridin-2-one
1H NMR (CD3OD, 300 MHz) δ 1.47-1.53 (m, 2H), 1.61-1.66 (m, 2H)5 1.74-1.78 (m, 2H), 3.48 (t, 2H)5 3.96 (t, 2H)5 4.45 (s, 2H), 5.06 (s, 2H)5 5.90 (s, IH), 5.94 (s, 2H), 6.06 (dd5 IH)5 6.61 (s, IH)5 6.90 (s, IH), 7.22-7.29 (m, 5H)5 7.42 (d, IH)
Example 82: l-(2-chloro-benzyl)-4-(3-methyl-butoxy) -lH-pyridin-2-one 1H NMR (CDCl3, 300 MHz) δ 0.93 (d, 6H)5 1.60-1.82 (m, 3H), 3.94 (t, 2H)5 5.17 (s, 2H), 5.86-5.94 (m, 2H)5 7.12-7.40 (m, 5H)
Example 83: l-(3,4-dichloro-benzyl)-4-(3-methyl-butoxy)-lH-pyridin-2-one
1H NMR (CDCl3, 300 MHz) δ 0.92 (d, 6H)5 1.63 (q, 2H)5 1.72-1.81 (m, IH)5 3.92 (t,
2H), 4.99 (s, 2H)5 5.87-5.90 (m, 2H)5 7.05-7.12 (m, 2H)5 7.33-7.38 (m, 2H)
Example 84: l-(254-dichloro-5-fluoro-benzyl)-4-(3-methyl-butoxy) -lH-pyridin-2-one 1H NMR (CDCl3, 300 MHz) δ 0.92 (d5 6H), 1.64 (q, 2H)5 1.71-1.82 (m, IH)5 3.93 (t, 2H), 5.08 (s, 2H), 5.90-5.92 (m, 2H)5 7.00 (d, IH)5 7.12-7.15 (m, IH), 7.42 (d, IH)
Example 85: l-benzyl-4-(3-methyl-butoxy)-lH-pyridin-2-one 1U NMR (CDCl3, 300 MHz) δ 0.95 (d, 6H), 1.59-1.78 (m, 3H), 3.93 (t, 2H)9 5.08 (s, 2H), 5.83-5.93 (m, 2H), 7.07-7.36 (m, 6H)
Example 86: l-(4-chloro-benzyl)-4-(3-methyl-butoxy)-lH-pyridin-2-one 1H NMR (CDCl3, 300 MHz) δ 0.92 (d, 6H), 1.62 (q, 2H), 1.71-1.80 (m, IH), 3.91 (t, 2H), 5.01 (s, 2H), 5.85 (dd, IH), 5.89 (d, IH), 7.06 (d, IH), 7.19 (d, 2H), 7.27 (d, 2H)
Example 87: 1 -(2,4-dichloro-benzyl)-4-pentyloxy-lH-pyrimidin-2-one 1H NMR (CDCl3, 300 MHz) δ 0.88 (t, 3H), 1.32-1.36 (m, 4H), 1.61-1.73 (m, 2H), 4.33 (t, 2H), 5.07 (s, 2H), 5.83 (d, IH), 7.22 (d, IH), 7.35-7.45 (m, 3H)
Example 88: l-(2,4-dichloro-benzyl)-4-(4-methyl-pentyloxy)-lH-pyrimidin-2-one 1H NMR (CDCl3, 300 MHz) δ 0.89 (d, 6H), 1.20-1.76 (m, 5H), 4.34 (t, 2H), 5.09 (s, 2H), 5.85 (d, IH), 7.22 (d, IH), 126-1 Al (m, 3H)
Example 89 : 1 -(2,4-dichloro-benzyl)-4-phenoxy- 1 H-pyrimidin-2-one
1H NMR (CDCl3, 300 MHz) δ 5.11 (d, 2H), 6.07 (d, IH), 7.12-7.65 (m, 9H)
Example 90 : 4-(butyl-methyl-amino)- 1 -(2,4-dichloro-benzyl)- 1 H-pyrimidin-2-one 1H NMR (CDCl3, 300 MHz) δ 0.90 (t, 3H), 1.19-1.56 (m, 4H), 2.81-3.11 (m, 3H), 3.22- 3.27 (m, IH), 3.59-3.62 (m, IH), 4.98 (s, 2H), 5.72-5.75 (m, IH), 7.12-7.31 (m, 4H)
Example 91: 1 -(2,4-dichloro-benzyl)-4-(2-diethylamino-ethoxy)- 1 H-pyrimidin-2-one 1R NMR (CDCl3, 300 MHz) δ 1.04 (t, 6H), 2.62 (q, 4H), 2.84 (t, 2H), 4.46 (t, 2H), 5.09 (s, 2H), 5.90 (d, IH), 7.21-7.54 (m, 4H)
Example 92: 4-butoxy-l-(2,4-dichloro~benzyl)-lH-pyrimidin-2-one 1H NMR (CDCl3, 300 MHz) δ 0.95 (t, 3H), 1.39-1.46 (m, 2H), 1.69-1.74 (m, 2H)5 4.37 (t, 2H), 5.10 (s, 2H), 5.87 (d, IH), 7.23-7.48 (m, 4H)
Example 93: 1 ~(2,6-dichloro-benzyl)-4-pentyloxy- lH-pyridin-2-one
1H NMR (CDCl3, 300 MHz) δ 0.91 (t, 3H), 1.32-1.44 (m, 4H), 1.70-1.80 (m, 2H), 3.90
(t, 2H), 5.37 (s, 2H), 5.79 (dd, IH), 5.91 (d, IH), 6.71 (d, IH)5 7.25-7.41 (m, 3H)
Example 94: 1 -(2-chloro-6-fluoro-benzyl)-4-pentyloxy-lH-pyridin-2-one
1H NMR (CDCl3, 300 MHz) δ 0.91 (t, 3H)5 1.30-1.44 (m, 4H), 1.70-1.77 (m, 2H), 3.89
(t, 2H), 5.24 (s, 2H)5 5.82 (dd5 IH), 5.88 (d, IH)5 6.92 (d, IH)5 7.05 (t, IH), 7.24-7.33
(m, 2H)
Example 95: 1 -(2-methyl-3-nitro-benzyl)-4-pentyloxy- lH-pyridin-2-one 1H NMR (CDCl3, 300 MHz) δ 0.92 (t, 3H)5 1.33-1.43 (m, 4H)5 1.75 (m, 2H)5 2.40 (s, 3H), 3.92 (t, 2H)5 5.13 (s, 2H)5 5.92-5.95 (m, 2H), 6.98 (dd, IH), 7.16 (d, IH)5 7.28 (t, IH)5 7.69 (d, IH)
Example 96: 1 -(3-amino-2-methyl-benzyl)-4-pentyloxy-lH-pyridin-2-one 1H NMR (CDCl3, 300 MHz) δ 0.92 (t, 3H), 1.33-1.43 (m, 4H), 1.71-1.80 (m, 2H)5 2.01 (s, 3H)5 3.72 (s5 2H), 3.91 (t, 2H), 5.05 (s, 2H)5 5.81 (dd, IH), 5.92 (d, IH), 6.56 (d, IH)5 6.69 (d, IH), 6.90 (d, IH), 7.01 (t, IH) Example 97: 1 -(4-methoxy-3,5-dimethyl-pyridin-2-ylmethyl)-4-pentyloxy-lH-pyridin- 2-one
1H NMR (CDCl3, 300 MHz) δ 0.92 (t, 3H), 1.30-1.41 (m, 4H), 1.70-1.77 (m, 2H), 2.23 (s, 3H), 2.30 (s, 3H), 3.75 (s, 3H), 3.89 (t, 2H), 5.16 (s, 2H), 5.85-5.88 (m, 2H), 7.28- 7.30 (m, IH), 8.19 (S5 IH)
Example 98: l-(6-chloro-benzo[l,3]dioxol-5-ylmethyl)-4-(5-hydroxy-pentyloxy) -IH- pyridin-2-one 1H NMR (CD3OD, 300 MHz) δ 1.48-1.58 (m, 4H), 1.75-1.80 (m, 2H)5 3.54 (t, 2H)5 3.97 (t, 2H), 5.06 (s, 2H), 5.89 (d, IH), 5.94 (s, 2H), 6.07 (dd, IH), 6.61 (s, IH), 6.90 (s, IH), 7.43 (d, IH)
Example 99 : 1 -(2-methoxy-5 -nitro-benzyl)-4-pentyloxy- 1 H-pyridin-2-one 1H NMR (CDCl3, 300 MHz) δ 0.92 (t, 3H), 1.36-1.44 (m, 4H), 1.74-1.80 (m, 2H), 3.91 (t, 2H), 3.97 (S, 3H), 5.07 (s, 2H), 5.90-5.95 (m, 2H), 7.17 (d, IH), 7.21 (d, IH), 8.03 (d, IH), 8.19 (dd, IH)
Example 100: l-(5-amino-2-methoxy-benzyl)-4-pentyloxy-l H-pyridin-2-one 1H NMR (CDCl3, 300 MHz) δ 0.92 (t, 3H), 1.24-1.39 (m, 4H), 1.73-1.78 (m, 2H), 3.79 (s, 2H), 3.90 (t, 2H), 5.02 (s, 2H), 5.83 (dd, IH), 5.89 (d, IH), 6.59-6.74 (m, 3H), 7.23- 7.27 (m, 3H)
Example 101: l-(2-ethyl-benzyl)-4-pentyloxy-l H-pyridin-2-one 1H NMR (CDCl3, 300 MHz) δ 0.93 (t, 3H)5 1.18 (t, 3H)5 1.34-1.43 (m, 4H)5 1.73-1.79 (m, 2H)5 2.63 (q, 2H)5 3.93 (t, 2H)5 5.12 (s, 2H)5 5.84 (dd, IH)5 5.94 (d, IH)5 6.92 (d, IH)5 7.05 (d, IH)5 7.16-7.32 (m, 3H)
Example 102: l-(2~chloro-5~nitro-benzyl)-4~pentyloxy-lH-pyridin-2-one
1H NMR (CDCl3, 300 MHz) δ 0.93 (t5 3H), 1.32-1.46 (m, 4H), 1.72-1.82 (m, 2H), 3.94 (t, 2H)5 5.19 (s, 2H)5 5.94 (dd, IH)5 6.00 (d, IH)5 7.18 (d, IH), 7.55 (d, IH)5 7.96 (d, IH), 9.09 (dd, IH)
Example 103: l-(5-amino-2-chloro-benzyl)-4-pentyloxy-lH-pyridin-2-one
1H NMR (CDCl3, 300 MHz) δ 0.93 (t, 3H), 1.31-1.43 (m, 4H)5 1.72-1.79 (m, 2H), 3.91 (t, 2H), 5.11 (s, 2H), 5.87-5.91 (m, 2H), 6.52-6.55 (m, 2H), 7.11-7.18 (m, 2H)
Example 104 : 1 -(4-methoxy-2,3 -dimethyl-benzyl)-4-pentyloxy- 1 H-pyridin-2-one 1H NMR (CDCl35 300 MHz) δ 0.93 (t, 3H), 1.31-1.42 (m, 4H), 1.72-1.81 (m, 2H)5 2,12 (s, 3H), 2.16 (s, 3H), 3.82 (s, 3H), 3.91 (t, 2H), 5.04 (s, 2H)5 5.80 (dd, IH)5 5.93 (d, IH), 6.71 (d, IH), 6.85 (d, IH)5 6.97 (d, IH)
Example 105: l-(2-methyl-pyridin-3-ylmethyl)-4-pentyloxy-l H-pyridin-2-one 1H NMR (CDCl3, 300 MHz) δ 0.93 (t, 3H), 1.32-1.47 (m, 4H), 1.73-1.83 (m, 2H), 2.56 (s, 3H), 3.93 (t, 2H)5 5.09 (s, 2H), 5.91-5.94 (m, 2H)5 7.00 (d, IH), 7.08-7.13 (m, IH), 7.26-7.28 (m, IH), 8.43 (d, IH)
Example 106: N-[4-chloro-3-(2-oxo-4-pentyloxy-2H-pyridin-l-ylmethyl)-phenyl]- acetamide
1H NMR (CDCl3, 300 MHz) δ 0.93 (t, 3H), 1.29-1.45 (m, 4H)3 1.71-1.78 (m, 2H), 2.10 (s, 3H), 3.87 (t, 2H)5 5.16 (s, 2H), 5.89 (d, IH)9 5.99 (dd, IH)5 7.26-7.33 (m. 3H), 7.77 (d, IH), 8.43 (br s, IH)
Example 107: 1 -(2,4-dichloro-benzyl)-4-(3-dimethylamino-propoxy)-lH-pyridin-2-one 1H NMR (CDCl3, 300 MHz) δ 1.87-1.97 (m, 2H), 2.25 (s, 6H), 2.40 (t, 2H), 4.42 (t, 2H), 5.10 (s, 2H), 5.87 (d, IH), 7.23-7.49 (m, 4H)
Example 108: l-(2,4-dichloro-benzyl)-4-(4-dimethylamino-butoxy)-lH-pyridin-2-one 1H NMR (CDCl3, 300 MHz) δ 1.52-1.81 (m, 4H)5 2.22 (s, 6H), 2.29 (t, 2H), 4.38 (t, 2H), 5.10 (s, 2H), 5.86 (d, IH), 7.23-7.48 (m, 4H)
Example 109: l-(254-dichloro-benzyl)-4-(6-dimethylamino-hexyloxy)-lH-pyrimidin-2- one
1H NMR (CDCl3, 300 MHz) δ 1.34-1.78 (m, 8H)5 2.24-2.30 (m, 8H)5 4.35 (t, 2H)5 5.10 (S5 2H)5 5.86 (d, IH), 7.23-7.47 (m, 4H)
Example 110 : 1 -(2,4-dimethyl-benzyl)-4-pentyloxy- 1 H-pyridin-2-one 1H NMR (CDCl3, 300 MHz) δ 0.92 (t, 3H)5 1.33-1.42 (m, 4H)5 1.71-1.76 (m, 2H)5 2.22 (S5 3H)5 2.31 (s5 3H)5 3.91 (t, 2H), 5.03 (s, 2H)5 5.83 (dd5 IH)5 5.92 (d, IH), 6.89-7.20 (m, 4H)
Example 111: 1 -(2-chloro-5-trifluoromethyl-benzyl)-4-pentyloxy- 1 H-pyridin-2-one 1H NMR (CDCl3, 300 MHz) δ 0.93 (t, 3H)5 1.34-1.46 (m, 4H)5 1.74-1.83 (m, 2H)5 3.93 (t, 2H)5 5.21 (s, 2H)5 5.94-6.15 (m, 2H)5 7.17 (d, IH)5 7.43-7.54 (m, 3H)
Example 112: l-(2-hydroxy-benzyl)-4-pentyloxy-lH-pyridin-2-one 1H NMR (CDCl35 300 MHz) δ 0.91 (t, 3H)5 1.29-1.43 (m, 4H), 1.70-1.79 (m, 2H)5 3.90 (t, 2H)5 4.99 (s5 2H)5 5.97 (d, IH), 6.04 (dd, IH)5 6.83 (t, IH)5 6.95 (dd, IH)5 7.19-7.24 (m, 2H)5 7.38 (d, IH)5 10.45 (br s, IH)
Example 113: 4-(3-cyclo-propoxy)-l -(2,4-dichloro-benzyl)-lH-pyrimidin-2-one 1H NMR (CDCl3, 300 MHz) δ 1.27-1.25 (m, 2H), 1.51-1.82 (m, 9H)5 4.37 (t, 2H)5 5.10 (S5 2H)5 5.85 (d, IH), 7.22 (d, IH)5 7.38-7.47 (m, 3H)
Example 114: l-(2,4-dichloro-benzyl)-4-(3-methyl-pentyloxy)-lH-pyrimidin-2-one 1H NMR (CDCl3, 300 MHz) δ 0.85-2.03 (m, HH)5 4.39 (t, 2H)5 5.10 (s, 2H)5 5.85 (d, IH), 122-1 Al (m, 4H)
Example 115 : 1 -(2,4-dichloro-benzyl)-4-hex-4-enyloxy- 1 H-pyrimidin-2-one 1H NMR (CDCl3, 300 MHz) δ 1.25-2.10 (m, 7H)5 4.35 (t, 2H)5 5.10 (s, 2H)5 5.40-5.46 (m, 2H)5 5.86 (d, IH)5 7.23-7 '.47 (m, 4H)
Example 116: 4-(2-cyclopropyl-ethoxy)-l-(2,4-dichloro-benzyl)-l H-pyrimidin-2-one 1H NMR (CDCl35 300 MHz) δ 0.42-0.96 (m, 3H)5 1.25-1.66 (m, 4H), 4.43 (t, 2H)5 5.10 (s, 2H), 5.87 (d5 IH)5 1.22-1 Al (m, 4H) Example 117: 1 -(2,4-dichloro-benzyl)-4-(3-methyl-pentyloxy)- 1 H-pyridin-2-one 1H NMR (CDCl3, 300 MHz) δ 0.85-0.91 (m, 6H), 1.17-1.24 (m, IH), 1.33-1.39 (m, IH), 1.51-1.58 (m, 2H), 1.78-1.80 (m, IH), 3.93 (t, 2H), 5.12 (s, 2H), 5.88-5.92 (m, 2H)5 7.14-7.20 (m, 3H)5 7.38 (s, IH)
Example 118: 1 -(2,4-dichloro-benzyl)-4-(5-morpholin-4-yl-pentyloxy)-lH-pyridin-2- one
1H NMR (CDCl3, 300 MHz) δ 1.46-1.61 (m, 4H), 1.75-1.84 (m, 2H), 2.36 (t, 2H), 2.44 (br s, 4H), 3.73 (t, 4H), 3.92 (t, 2H), 5.14 (s, 2H), 5.90-5.92 (m, 2H), 7.16-7.23 (m, 3H)5 7.41 (s, IH)
Example 119: 1 -(2-chloro-5-methoxy-benzyl)-4-pentyloxy-lH-pyridin-2-one 1H NMR (CDCl3, 300 MHz) δ 0.93 (t, 3H), 1.33-1.43 (m, 4H), 1.72-1.79 (m, 2H), 3.74 (s, 3H), 3.91 (t, 2H), 5.15 (s, 2H), 5.88-5.93 (m, 2H), 6.76-6.79 (m, 2H), 7.15 (d, IH), 7.27 (d, IH)
Example 120: l-(2-chloro-5-ethoxy-benzyl)-4-pentyloxy-lH-pyridin-2-one 1H NMR (CDCl3, 300 MHz) δ 0.93 (t, 3H), 1.25-1.40 (m, 7H), 1.72-1.81 (m, 2H), 3.89- 3.99 (m, 4H), 5.15 (s, 2H), 5.89-5.92 (m, 2H), 6.75-6.77 (m, 2H), 7.15 (d, IH), 7.26 (d, IH)
Example 121: l-(2-chloro-5-propoxy-benzyl)-4-pentyloxy-lH-pyridin-2-one
1H NMR (CDCl3, 300 MHz) δ 0.93 (t, 3H), 1.00 (t, 3H), 1.33-1.43 (m, 4H), 1.70-1.81
(m, 4H), 3.84 (t, 2H), 3.92 (t, 2H), 5.15 (s, 2H), 5.88-5.93 (m, 2H), 6.74-6.78 (m, 2H), 7.15 (d, IH), 7.26 (d, IH)
Example 122 : 1 - [2-chloro-5-(2-hydroxy-ethoxy)-benzyl] -4-pentyloxy- 1 H-pyridin-2- one 1H NMR (CDCl3, 300 MHz) δ 0.90 (t, 3H)5 1.25-1.43 (m, 4H), 1.72-1.79 (m, 2H), 2.13 (t, IH), 3.91 (t, 4H), 4.01 (t, 2H), 5.15 (s, 2H), 5.86-5.92 (m, 2H)3 6.76-6.83 (m, 2H), 7.18 (d, IH), 7.28 (d, IH)
Example 123: [4-chloro-3-(2-oxo-4-pentyloxy-2H-pyridin- 1 -ylmethyl)-oxy]- acetonitrile
1H NMR (CDCl3, 300 MHz) δ 0.93 (t, 3H), 1.33-1.43 (m, 4H), 1.73-1.82 (m, 2H), 3.92 (t, 2H), 4.71 (s, 2H)5 5.16 (s, 2H), 5.92-5.95 (m, 2H), 6.84-6.88 (m, 2H), 7.20 (d, IH)5 7.35 (dd, IH)
Example 124: l-[5-(2-amino-ethoxy)-2-chloro-benzyl]-4-pentyloxy-lH-pyridin-2-one 1H NMR (CDCl3, 300 MHz) δ 0.93 (t, 3H), 1.41-1.44 (m, 4H), 1.78-1.82 (m, 2H), 3.93 (t, 2H), 4.01 (t, 4H)5 5.17 (s, 2H)5 5.96 (d, IH)5 7.13 (dd, IH)5 6.60 (s, IH), 6.90 (d5 IH), 7.34 (d, IH), 7.49 (d, IH)
Example 125: N-[2-methyl-3-(2-oxo-4-pentyloxy-2H-pyridin-l-ylmethyl)-phenyl]- acetamide
1H NMR (CDCl3, 300 MHz) δ 0.93 (t, 3H), 1.34-1.44 (m, 4H)5 1.73-1.82 (m, 2H), 2.07 (S5 3H)5 2.22 (s, 3H), 3.92 (t, 2H)5 5.05 (s, 2H), 5.89 (dd, IH), 5.93 (d, IH)5 6.84 (d, IH)5 6.94 (d5 IH), 7.18 (t, IH), 7.49 (br s, IH), 7.56 (d, IH) Example 126: 1 -(2-methyl-3-methylamino-benzyl)-4-phenyloxy-lH-pyridin-2-one 1H NMR (CDCl3, 300 MHz) δ 0.92 (t, 3H), 1.27-1.40 (m, 4H), 1.73-1.78 (m, 2H), 1.98 (s, 3H), 2.90 (s, 3H), 3.69 (br s, IH), 3.90 (t, 2H), 5.07 (s, 2H), 5.80 (dd, IH), 5.93 (d, IH), 6.57 (d, IH), 6.65 (d, IH), 6.89 (d, IH), 7.16 (t, IH)
Example 127: l-(3-dimethylamino-2-methyl-benzyl)-4-phenyloxy-lH-ρyridin-2-one 1H NMR (CDCl3, 300 MHz) δ 0.93 (t, 3H), 1.36-1.43 (m, 4H), 1.75-1.79 (m, 2H), 2.22 (S5 3H), 2.69 (s, 6H), 3.92 (t, 2H)5 5.07 (s, 2H), 5.86 (dd, IH), 5.95 (d, IH)5 6.72 (d, IH), 6.93 (d, IH), 7.05 (d, IH)5 7.15 (t, IH)
Example 128: l-(3-ethylamino-2-methyl-benzyl)-4-pentyloxy-lH-pyridin-2-one 1H NMR (CDCl3, 300 MHz) δ 0.92 (t, 3H), 1.31 (t, 3H), 1.33-1.42 (m, 4H)5 1.71-1.78 (m, 2H)5 1.97 (s, 3H), 3.19 (q, 2H), 3.48 (br s, IH)5 3.90 (t, 2H)5 5.06 (s, 2H), 5.79 (dd, IH)5 5.93 (d, IH), 6.56 (d, IH), 6.65 (d, IH)5 6.89 (d, IH), 7.13 (t, IH)
Example 129: l-(3-diethylamino-2-methyl-benzyl)-4-pentyloxy-lH-pyridin-2-one 1H NMR (CDCl3, 300 MHz) δ 0.96 (t, 9H)5 1.34-1.44 (m, 4H), 1.75-1.80 (m, 2H), 2.21 (s, 3H), 2.95 (q, 4H), 3.92 (t, 2H), 5.08 (s, 2H), 5.87-5.95 (m, 2H), 6.73 (d, IH)5 6.95- 7.16 (m, 3H)
Example 130: l-(2-methyl-3-propylamino-benzyl)-4-pentyloxy-lH-pyridin-2-one
1H NMR (CDCl3, 300 MHz) δ 0.93 (t, 3H), 1.02 (t, 3H), 1.33-1.42 (m, 4H)5 1.66-1.80
(m, 4H), 1.97 (s, 3H), 3.12 (t, 2H)5 3.57 (br s, IH), 3.91 (t, 2H), 5.06 (s, 2H), 5.80 (dd, IH), 5.93 (d, IH)5 6.55 (d, IH), 6.65 (d, IH)5 6.90 (d, IH)5 7.13 (t, IH)
Example 131: l-(3-dipropylamino-2-methyl-benzyl)-4-pentyloxy-lH-pyridin-2-one 1H NMR (CDCl35 300 MHz) δ 0.83 (t, 6H), 0.93 (t, 3H)5 1.34-1.47 (m, 8H)5 1.75-1.80 (m5 2H)5 2.22 (s, 3H), 2.82-2.87 (m, 4H)5 3.93 (t, 2H)5 5.07 (s, 2H)5 5.87 (dd5 IH)5 5.96 (d, IH)5 6.69 (d, IH)5 6.94 (d, IH), 7.07-7.15 (m, 2H)
Example 132: l-[3-(2-hydroxy-ethylamino)-2-methyl-benzyl]-4-pentyloxy-lH-pyridin- 2-one 1H NMR (CDCl3, 300 MHz) δ 0.92 (t, 3H)5 1.32-1.41 (m, 4H), 1.71-1.78 (m, 2H), 1.83 (br s, IH), 2.01 (s, 3H), 3.34 (t, 2H), 3.90 (t, 4H)5 4.02 (br S5 IH), 5.06 (s, 2H)5 5.81 (dd, IH), 5.92 (d, IH), 6.57 (d, IH)5 6.67 (d, IH), 6.89 (d, IH), 7.12 (t, IH)
Example 133: l-(2-chloro-5-methoxy-4-nitro-benzyl)-4-pentyloxy-lH-pyridin-2-one 1H NMR (CDCl3, 300 MHz) δ 0.94 (t, 3H)5 1.37-1.44 (m, 4H)5 1.76-1.81 (m, 2H), 3.91 (s, 3H), 3.93 (t, 2H)5 5.20 (s, 2H)5 5.93 (d, IH), 5.97 (dd, IH), 7.18 (s, IH)5 7.26 (d, IH)5 7.93 (s5 IH)
Example 134: l-(4-amino-2-chloro-5-methoxy-benzyl)-4-pentyloxy-lH-pyridin-2-one 1H NMR (CDCl35 300 MHz) δ 0.92 (t, 3H)5 1.32-1.42 (m, 4H)5 1.71-1.78 (m, 2H), 3.81 (t, 3H), 3.87-3.93 (m, 4H)5 5.09 (s, 2H)5 5.85 (dd, IH)5 5.90 (d, IH), 6.69 (s, IH), 6.91 (s5 IH), 7.21 (d, IH)
Example 135: N-[5-chloro-2-methoxy-4-(2-oxo-4-pentyloxy-2H-pyridin-l-ylmethyl)- phenyl] -acetamide
1H NMR (CDCl3, 300 MHz) δ 0.92 (t, 3H), 1.35-1.42 (m, 4H), 1.74-1.78 (m, 2H), 2.21 (s, 3H), 3.84 (s, 3H), 3.90 (t, 2H), 5.15 (s, 2H), 5.88-5.93 (m, 2H), 7.04 (s, IH), 7.29 (d, IH), 7.77 (br s, IH), 8.46 (ss IH)
Example 136: 1 -(2-chloro-5-methoxy-4-methylamino-benzyl)-4-pentyloxy- 1 H-pyridin- 2-one
1H NMR (CDCl3, 300 MHz) δ 0.93 (t, 3H), 1.30-1.43 (m, 4H), 1.70-1.77 (m, 2H), 2.85 (s, 3H), 3.81 (s, 3H), 3.92 (t, 2H), 4.95 (s, 2H), 5.89-6.03 (m, 2H), 6.53 (s, IH), 6.89 (s, IH), 7.28 (d, IH)
Example 137 : 1 -(2-chloro-4-dimethylamino-5-methoxy-benzyl)-4-pentyloxy- 1 H- pyridin-2-one
1H NMR (CDCl3, 300 MHz) δ 0.95 (t, 3H), 1.40-1.44 (m, 4H), 1.75-1.81 (m, 2H), 2.76 (s, 6H), 3.80 (s, 3H), 3.99 (t, 2H), 5.14 (s, 2H), 5.95 (d, IH), 6.10 (dd, IH), 6.85 (s, IH), 7.00 (s, IH), 7.47 (d, IH)
Example 138 : 1 -(2-chloro-4-ethylamino-5-methoxy-benzyl)-4-pentyloxy- 1 H-pyridin- 2-one 1H NMR (CDCl3, 300 MHz) δ 0.92 (t, 3H), 1.28 (t, 3H), 1.36-1.41 (m, 4H), 1.71-1.77 (m, 2H), 3.13 (t, 2H), 3.80 (s, 3H), 3.89 (t, 2H), 4.23 (br s, IH), 5.10 (s, 2H), 5.84 (dd, IH), 5.90 (d, IH), 6.52 (s, IH), 6.87 (s, IH), 7.22 (d, IH)
Example 139: l-(2-chloro-5-methoxy-4-propylamino-benzyl)-4-pentyloxy-lH-pyridin- 2-one
1H NMR (CDCl3, 300 MHz) δ 0.92 (t, 3H), 1.00 (t, 3H), 1.34-1.41 (m, 4H)3 1.62-1.77 (m, 4H), 3.05 (t, 2H), 3.80 (s, 3H), 3.89 (t, 2H), 4.31 (br s, IH), 5.09 (s, 2H), 5.83 (dd, IH), 5.89 (d, IH), 6.51 (s, IH), 6.86 (s, IH), 7.21 (d, IH)
Example 140: 1 -[2-chloro-4-(2-hydroxy-ethylamino)-5-methoxy-benzyl]-4-pentyloxy- lH-pyridin-2-one
1H NMR (CDCl3, 300 MHz) δ 0.92 (t, 3H), 1.32-1.42 (m, 4H), 1.70-1.77 (m, 2H), 1.96 (br s, IH), 3.30 (t, 2H), 3.79 (s, 3H), 3.82-3.91 (m, 4H), 4.73 (br s, IH), 5.09 (s, 2H), 5.85 (dd, IH), 5.90 (d, IH), 6.57 (s, IH), 6.88 (s, IH), 7.21 (d, IH)
Example 141 : 1 -(4-amino-6-chloro-3-methoxy-2-nitro-benzyl)-4-pentyloxy- 1 H- pyridin-2-one
1H NMR (CDCl3, 300 MHz) δ 0.91 (t, 3H), 1.28-1.41 (m, 4H), 1.69-1.79 (m, 2H), 3.84 (s, 3H), 3.88 (t, 2H), 4.35 (br s, 2H), 4.96 (s, 2H), 5.82-5.85 (m, 2H), 6.92-7.02 (m, 2H)
Example 142: l-(2,4-diamino-6-chloro-3-methoxy-benzyl)-4-pentyloxy-lH-pyridin-2- one
1H NMR (CDCl3, 300 MHz) δ 0.92 (t, 3H), 1.30-1.39 (m, 4H), 1.73-1.77 (m, 2H), 3.69 (s, 3H), 3.79 (br s, 2H), 3.89 (t, 2H), 5.16 (s, 2H), 5.30 (br s, 2H), 5.88-5.94 (m, 2H)5 6.17 (s, IH), 7.56 (d, IH)
Example 143: 1 -(2,5-dichloro-6-methoxy-pyrimidin-4-ylmethyl)-4-pentyloxy-lH- pyridin-2-one H NMR (CDCl3, 300 MHz) δ 0.93 (t, 3H), 1.34-1.45 (m, 4H), 1.73-1.82 (m, 2H), 3.92 (t, 2H), 4.08 (s. 3H), 5.14 (s, 2H), 5.86 (d, IH), 5.96 (dd, IH), 7.19 (d, IH)
Example 144: l-(2,4-dichloro-benzenesulfonyl)-4-pentyloxy-lH-pyridin-2-one 1H NMR (CDCl3, 300 MHz) δ 0.90 (t, 3H), 1.32-1.40 (m, 4H), 1.72-1.79 (m, 2H), 3.89 (t, 2H), 5.60 (d, IH), 6.05 (dd, IH), 7.47-7.51 (m, 2H)5 7.95 (d, IH), 8.35 (d, IH)
Example 145: 1 -(4-methanesulfonyl-benzyl)-4-pentyloxy-lH-pyridin-2-one 1H NMR (CDCl3, 300 MHz) δ 0.94 (t, 3H), 1.34-1.45 (m, 4H), 1.74-1.83 (m, 2H), 3.04 (s, 3H), 3.94 (t, 2H)5 5.22 (s, 2H)5 5.93 (d, IH), 5.99 (dd, IH), 7.20 (d, IH), 7.32 (d, IH), 7.76 (dd, IH), 7.97 (d, IH)
Example 146: 1 -(4-amino-2-chloro-5-hydroxy-benzyl)-4-pentyloxy- 1 H-pyridin-2-one 1H NMR (CDCl3, 300 MHz) δ 0.91 (t, 3H), 1.29-1.41 (m, 4H), 1.66-1.75 (m, 2H), 3.78 (t, 2H), 5.13 (s, 2H), 5.85 (d, IH), 5.94 (dd, IH), 6.68 (s, IH), 7.18 (s, IH), 7.44 (d, IH)
Example 147: 4-(4-bromo-butoxy)-l-(2,4-dichloro-benzyl) -1 H-pyridin-2-one 1H NMR (CDCl3, 300 MHz) δ 1.88-2.08 (m, 4H), 3.46 (t, 2H), 3.95 (t, 2H), 5.13 (s, 2H), 5.88-5.92 (m, 2H), 7.16-7.24 (m, 3H), 7.40 (s, IH)
Example 148 : 4-[ 1 -(2,4-dichloro-benzyl)-2-oxo- 1 ,2-dihydro-pyridin-4-yloxy] - butylammonium
1R NMR (CD3OD, 300 MHz) δ 1.82-1.90 (m, 4H), 3.00 (t, 2H)5 4.07 (t, 2H), 5.19 (s,
2H), 5.97 (s, IH), 6.14 (dd, IH), 7.05 (d, IH), 7.31 (dd, IH), 7.53-7.57 (m, 2H) Example 149: l-(5-chloro-2,6-dimethoxy-pyrimidin-4-ylmethyl)-4-pentyloxy-lH- pyridin-2-one
1H NMR (CDCl3, 300 MHz) δ 0.93 (t, 3H), 1.32-1.40 (m, 4H), 1.73-1.80 (m, 2H), 3.80 (s, 3H), 3.91 (t, 2H), 4.04 (s, 3H), 5.15 (s, 2H)5 5.89 (d, IH), 5.93 (dd, IH), 7.16 (d, IH)
Example 150: 1 -(2-amino-5-chloro-6-methoxy-pyrimidin-4-ylmethyl)-4-pentyloxy-lH- pyridin-2-one
1H NMR (CDCl3, 300 MHz) δ 0.93 (t, 3H), 1.32-1.43 (m, 4H), 1.73-1.80 (m, 2H), 3.92 (t, 2H), 3.95 (s, 3H), 4.81 (br s, 2H), 5.08 (s, 2H), 5.90-5.93 (m, 2H), 7.10 (d, IH)
Example 151 : 1 -(6-amino-2,5-dichloro-pyrimidin-4-ylmethyl)-4-pentyloxy- 1 H- pyridin-2-one
1H NMR (CDCl3, 300 MHz) δ 0.95(t, 3H), 1.31-1.44 (m, 4H), 1.73-1.79 (m, 2H), 3.91 (t, 2H), 5.08 (s, 2H), 5.60 (br s, 2H), 5.86 (d, IH), 5.95 (dd, IH), 7.22 (d, IH)
Example 152: 5-chloro-6-(2-oxo-4-pentyloxy-2H-pyridin-l-ylmethyl)-3H- benzoxazole-2-one
1H NMR (CDCl3, 300 MHz) δ 0.94 (t, 3H), 1.38-1.46 (m, 4H), 1.76-2.05 (m, 2H), 3.97 (t, 2H), 5.11 (s, 2H), 6.01-6.07 (m, 2H), 6.72 (s, IH), 6.73 (s, IH), 7.22 (d, IH), 9.35 (br s, lH)
Example 153 : 1 -(2-chloro-4-hydroxy-benzyl)-4-pentyloxy- 1 H-pyridin-2-one
1H NMR (CDCl3, 300 MHz) δ 0.92 (t, 3H), 1.30-1.41 (m, 4H), 1.70-1.80 (m, 2H)5 3.90 (t, 2H)5 5.09 (s, 2H)5 5.94-6.01 (m, 2H), 6.60 (dd, IH)5 6.88 (d, IH)5 7.00 (d, IH)5 7.28 (d, IH)5 9.75 (br s, IH)
Example 154: l-(2-chloro-4-isopropoxy-benzyl)-4-pentyloxy-lH-pyridin-2-one 1H NMR (CDCl35 300 MHz) δ 0.92 (t, 3H)5 1.31 (d, 6H), 1.35-1.45 (m, 4H)5 1.73-1.80 (m, 2H)5 3.90 (t, 2H)5 4.46-4.54 (m. IH), 5.11 (s, 2H)3 5.85-5.91 (m, 2H), 6.74 (dd, IH), 6.91 (d, IH), 7.16 (d IH), 7.23 (d, IH)
Example 155: 2-[3-(2-oxo-4-pentyloxy-2H-pyridin-l-yl)-propyl]-isoindole-l,3-dione 1H NMR (CDCl3, 300 MHz) δ 0.93 (t, 3H)5 1.20-1.33 (m, 4H)5 1.71-1.80 (m, 2H)5 2.09- 2.18 (m, 2H), 3.75 (t, 2H)5 3.87-3.94 (m, 4H)5 5.86 (d, IH), 5.91 (dd, IH), 7.27 (s, IH), 7.72-7.76 (m, 2H), 7.83-7.87 (m, 2H) .
Example 156: l-(3-amino-propyl)-4-pentyloxy-lH-pyridin-2-one 1H NMR (CDCl3, 300 MHz) δ 0.93 (t, 3H), 1.36-1.44 (m, 4H), 1.75-1.80 (m, 2H)5 2.26- 2.30 (m, 2H)5 3.00 (t, 2H)5 3.91 (t, 2H), 4.10 (t, 2H), 5.90 (d, IH), 6.02 (d, IH)5 7.25 (d, IH)
Example 157: N-[3-(2-oxo-4-pentyloxy-2H-pyridin- 1 -yl)-propyl]-acetamide 1H NMR (CDCl3, 300 MHz) δ 0.93 (t, 3H), 1.34-1.44 (m, 4H), 1.73-1.89 (m, 4H)5 2.01 (s, 3H), 3.15-3.21 (m, 2H), 3.92 (t, 2H)5 3.98 (t, 2H), 5.89 (d, IH), 5.98 (dd, IH), 7.08 (br s, IH)5 7.14 (d, IH)
Example 158: l-(3-dimethylamino-propyl)-4-pentyloxy-lH-pyridin-2-one 1H NMR (CDCl3, 300 MHz) δ 0.93 (t, 3H), 1.37-1.42 (m, 4H), 1.72-1.78 (m, 4H)5 2.31-
2.39 (m, 2H)5 3.16-3.20 (m, 2H), 3.40 (s, 6H)5 3.90 (t, 2H)5 4.11 (t, 2H)5 5.84 (s, IH), 5.97 (d, IH)5 7.55 (d, IH)
Example 159: l-(254-dichloro-benzyl)-6-methyl-4-pentyloxy-lH-pyridin-2-one
1H NMR (CDCl3, 300 MHz) δ 0.93 (t, 3H), 1.34-1.44 (m, 4H), 1.73-1.92 (m, 2H)5 2.13 (S5 3H), 3.93 (t, 2H), 5.28 (d, 2H), 5.82 (d, IH), 5.88 (d, IH), 6.72 (d, IH), 7.13 (d, IH),
7.40 (d, IH)
Example 160: l-(2,4-dichloro-benzyl)-6-methyl-3-pentyl-4-pentyloxy-lH-pyridin-2- one
1H NMR (CDCl3, 300 MHz) δ 0.85-0.98 (m. 6H), 1.30-1.48 (m, 10H), 1.75-1.78 (m,
2H), 2.18 (s, 3H), 2.55 (t, 2H), 3.99 (t, 2H)5 5.33 (s, 2H)5 5.94 (s, IH), 6.65 (d, IH)5 7.12
(dd, IH), 7.39 (d, IH)
Example 161: l-(2-amino-ethyl)-4-pentyloxy-lH-pyridin-2-one
1H NMR (CDCl3 + a few drop Of CD3OD, 300 MHz) δ 0.93 (t, 3H)5 1.31-1.40 (m, 4H)5
1.75-1.79 (m, 2H), 2.95 (t, 2H), 3.81-4.00 (m, 4H)5 5.83-5.91 (m, 2H), 7.08 (d, IH)
Example 162: N-[2-(2-oxo-4-pentyloxy-2H-pyridin-l-yl)-ethyl]-acetamide
1H NMR (CDCl35 300 MHz) δ 0.92 (t, 3H)5 1.31-1.42 (m, 4H)5 1.72- 1.79 (m, 2H), 1.96 (s, 3H), 3.53 (q, 2H), 3.90 (t, 2H), 4.05 (t, 2H), 5.87 (d, IH)5 5.94 (dd, 2H), 6.89 (br s, IH), 7.13 (d, IH) Example 163: N-[l,l-dimethyl-2-(2-oxo-4-pentyloxy-2H-pyridin-l-yl)-ethyl]- methanesulfonamide
1H NMR (CDCl3, 300 MHz) δ 0.93 (t, 3H), 1.29-1.46 (m, 10H)5 1.75-1.80 (m, 2H), 2.98 (s, 3H)5 3.92 (t, 2H), 3.99 (s, 2H), 5.91-5.97 (m, 2H), 6.56 (br s, IH), 7.23 (d, IH)
Example 164: N-[I -(2-oxo-4-pentyloxy-2H-pyridin-l-ylmethyl)-propyl]- methanesulfonamide
1H NMR (CDCl3, 300 MHz) δ 0.93 (t, 3H), 1.05 (t, 3H), 1.30-1.40 (m, 4H), 1.59-1.81 (m, 4H), 2.75 (s, 3H)5 3.65-4.15 (m, 6H), 5.75 (d, IH), 5.91 (d, IH), 5.97 (dd, IH), 7.19 (d, IH)
Example 165: l-(7-nitro-benzo[l,3]dioxol-5-ylmethyl)-4-pentyIoxy-lH-pyridin-2-one 1H NMR (CDCl3, 300 MHz) δ 0.95 (t, 3H), 1.32-1.42 (m, 4H), 1.75-1.82 (m, 2H), 3.95 (t, 2H), 5.42 (s, 2H), 5.94-6.00 (m, 2H), 6.09 (s, 2H)5 6.55 (s, IH), 7.18 (d, IH), 7.63 (s, IH)
Example 166: 1 -(2-chloro-3 -nitro-benzyl)-4-pentyloxy- 1 H-pyridin-2-one 1H NMR (CDCl3, 300 MHz) δ 0.97 (t, 3H), 1.27-1.53 (m, 4H), 1.77-1.82 (m, 2H)5 3.95 (t, 2H), 5.25 (s5 2H)5 5.96-6.00 (m, 2H)5 7.22 (d, IH), 7.35-7.44 (m, 2H), 7.73 (d, IH)
Example 167: 1 -(3 -amino-2-chloro-benzyl)-4-pentyloxy-l H-pyridin-2-one 1U NMR (CDCl3, 300 MHz) δ 0.91 (t, 3H)5 1.37-1.43 (m, 4H)5 1.72-1.76 (m, 2H), 3.89 (t, 2H)5 4.13 (br s), 5.12 (s, 2H)5 5.86-5.92 (m, 2H)5 6.47 (d, IH)5 6.70 (d, IH)5 6.96- 7.07 (m, 2H) Example 168: N-[2-chloro-3-(2-oxo-4-pentyloxy-2H-pyridin-l-ylmethyl)-phenyl]- acetamide
1H NMR (CDCl3, 300 MHz) δ 0.94 (t, 3H), 1.27-1.44 (m, 4H)5 1.74-1.81 (m, 2H), 2.26 (s, 3H), 3.93 (t, 2H), 5.19 (s, 2H), 5.90-5.94 (m, 2H)5 6.87 (d, IH), 7.06 (d, IH), 7.23 (d, IH), 7.69 (br s, IH), 8.30 (d, IH)
Example 169: N-[25chloro-3-(2-oxo-4-pentyloxy-2H-pyridin-l -ylmethyl)-phenyl]- methanesulfonamide 1H NMR (CDCl35 300 MHz) δ 0.94 (t, 3H), 1.37-1.43 (m, 4H), 1.75-1.81 (m, 2H), 3.03 (s, 3H)5 3.94 (t, 2H), 5.18 (s, 2H), 5.94-5.97 (m, 2H), 6.90 (d, IH), 7.00 (br s, IH), 7.12 (d, IH)5 7.28 (d, IH), 7.60 (d, IH)
Example 170: N,N'-[2-chloro-3-(2-oxo-4-pentyloxy-2H-pyridin-l-ylmethyl)-phenyl]- dimethanesulfonamide
1H NMR (CDCl3, 300 MHz) δ 0.94 (t, 3H), 1.26-1 Al (m, 4H), 1.76-1.81 (m, 2H), 3.49 (s, 6H), 3.94 (t, 2H), 5.23 (s, 2H), 5.94-5.96 (m, 2H), 7.15 (d, IH), 7.25-7.38 (m, 3H)
Example 171: l-[2-chloro-3-(2-hydroxy-ethylamino)-benzyl]-4-pentyloxy-lH-pyridin- 2-one
1H NMR (CDCl3, 300 MHz) δ 0.93 (t, 3H)5 1.28-1.38 (m, 4H), 1.74-1.79 (m, 2H)5 2.00 (br s, IH), 3.37 (br s, 2H), 3.89-3.94 (m, 4H)5 4.74 (br s, IH)5 5.15 (s, 2H)5 5.87 (dd, IH), 5.93 (d, IH), 6.48 (d, IH)5 6.66 (d, IH)5 7.05-7.12 (m, 2H) Example 172: 4-chloro-2-(2-chloro-benzyl)-5-pentyloxy-2H-pyridazin-3-one
1H NMR (CDCl3, 300 MHz) δ 0.91 (t, 3H)5 1.30-1.47 (m, 4H), 1.70-1.79 (m, 2H), 4.59
(t, 2H), 5.43 (s, 2H)5 7.07-7.10 (m, IH), 7.18-7.26 (m, 2H)5 7.38 (dd, IH), 7.74 (s, IH)
Example 173: 2-(2-chloro-benzyl)-5-pentyloxy-2H-pyridazin-3-one
1H NMR (CDCl3, 300 MHz) δ 0.93 (t, 3H), 1.26-1.49 (m, 4H), 1.85-1.94 (m, 2H), 3.99 (t, 2H), 5.49 (s, 2H), 6.38 (d, IH), 7.16- 7.39 (m, 4H), 7.67 (d, IH)
Example 174: l-(3-amino-2,6-dichloro-benzyl)-4-pentyloxy-lH-pyridin-2-one 1H NMR (CDCl3, 300 MHz) δ 0.92 (t, 3H)3 1.25-1.44 (m, 4H)5 1.70-1.80 (m, 2H), 3.90 (t, 2H)5 4.19 (s5 2H)5 5.33 (s, 2H), 5.79 (dd, IH)5 5.92 (d, IH), 6.74 (dd, 2H), 7.18 (d, IH)
Example 175: 1 -(3-benzyloxy-2-chloro-4-methoxy-benzyl)-4-pentyloxy- lH-pyridin-2- one
1H NMR (CDCl3, 300 MHz) δ 0.91 (t, 3H)5 1.35-1.43 (m, 4H), 1.72-1.79 (m, 2H)5 3.84 (s5 3H)5 3.90 (t, 2H)5 5.02 (s, 2H)5 5.12 (s, 2H)5 5.84-5.91 (m, 2H)5 6.79 (d, IH)5 7.01 (d, IH)5 7.11 (d, IH), 7.33-7.40 (m, 3H), 7.49-7.54 (m, 2H)
Example 176: l-(2-chloro-3,4-dimethoxy-benzyl)-4-pentyloxy-lH-pyridin-2-one
1R NMR (CDCl3, 300 MHz) δ 0.94 (t, 3H), 1.27-1.41 (m, 4H), 1.74-1.80 (m, 2H)5 3.86- 3.94 (m, 8H)5 5.13 (s, 2H), 5.87-5.92 (m, 2H)5 6.80 (d, IH)5 7.03 (d, IH), 7.18 (d, IH)
Example 177: l-(2-chloro-3-hydroxy-4-methoxy-benzyl)-4-pentyloxy-lH-pyridin-2- one
1H NMR (CDCl3, 300 MHz) δ 0.95 (t, 3H), 1.26-1.39 (m, 4H), 1.73-1.76 (m, 2H), 3.89-
3.93 (m, 5H), 5.13 (s, 2H), 5.86-5.90 (m, 2H), 6.75 (d, IH), 6.83 (d, IH), 7.13 (d, IH)
Example 178: l-[2-chloro-4-methoxy-3-(2-methoxy-ethoxy)-benzyl]-4-pentyloxy-lH- pyridin-2-one
1H NMR (CDCl3, 300 MHz) δ 0.92 (t, 3H), 1.26-1.39 (m, 4H), 1.74-1.82 (m, 2H), 3.45
(s, 3H), 3.74 (t, 2H), 3.84 (s, 3H), 3.91 (t, 2H), 4.15 (t, 2H), 5.12 (s, 2H)S 5.86-5.91 (m,
2H), 6.78 (d, IH), 7.00 (d, IH), 7.15 (d, IH)
Example 179: l-[2-chloro-4-methoxy-3-(2-pyrrolidin-l-yl-ethoxy)-benzyl]-4- pentyloxy- 1 H-pyridin-2-one
1H NMR (CDCl3, 300 MHz) δ 0.93 (t, 3H), 1.33-1.39 (m, 4H), 1.77-1.84 (m, 6H), 2.71
(m, 4H), 2.97 (t, 2H), 3.83 (s, 3H), 3.91 (t, 2H), 4.13 (t, 2H), 5.12 (s, 2H), 5.86-5.92 (m, 2H), 6.78 (d, IH), 7.00 (d, IH), 7.15 (d, IH)
Example 180: 1 -[2-chloro-3-(2-dimethylammo-ethoxy)-4-methoxy-benzyl]-4- pentyloxy- 1 H-pyridin-2-one
1H NMR (CDCl3, 300 MHz) δ 0.94 (t, 3H), 1.33-1.42 (m, 4H), 1.75-1.82 (m, 2H), 2.41 (s, 6H), 2.83 (t, 2H), 3.97 (t, 2H), 4.11 (t, 2H), 5.13 (s, 2H), 5.94 (s, IH), 6.04 (dd, IH), 6.87 (dd, IH), 6.94 (dd, IH), 7.27 (d, IH)
Example 181: 2-{3-[2-chloro-6-methoxy-3-(2-oxo-4-pentyloxy-2H-pyridin-l- ylmethyl)-phenoxyl] -propyl } -isoindole- 1 ,3 -dione 1K NMR (CDCl3, 300 MHz) δ 0.92 (t, 3H), 1.28-1.38 (m, 4H), 1.73-1.77 (m, 2H), 3.59 (s, 3H), 3.89 (t, 2H)5 4.12 (t, 2H)5 4.26 (t, 2H), 5.03 (s, 2H)5 5.85-5.91 (m, 2H), 6.69 (d, IH)5 6.95 (d, IH), 7.08 (d, IH)5 7.74 (d, 2H), 7.87 (d, 2H)
Example 182: l-[3-(2-dimethylamino-ethoxy)-2-methyl-benzyl]-4-pentyloxy-lH- pyridin-2-one
1H NMR (CDCl35 300 MHz) δ 0.94 (t, 3H), 1.26-1.35 (m, 4H)5 1.75-1.79 (m, 2H), 2.15
(s, 3H)5 2.37 (s5 6H), 2.79 (t, 2H), 3.93 (t, 2H), 4.09 (t, 2H), 5.08 (s, 2H)5 5.83-5.94 (m,
2H)5 6.70 (d, IH), 6.83-6.92 (m, 2H)5 7.15 (t, IH)5 7.28 (s, IH)
Example 183: l-[2-chloro-3-(2-dimethylamino-ethylamino)-benzyl]-4-pentyloxy-lH- pyridin-2-one
1H NMR (CDCl3, 300 MHz) δ 0.93 (t, 3H)5 1.30-1.40 (m, 4H)5 1.55-1.59 (m, 2H)5 2.29
(s, 6H), 2.62 (t, 2H)5 3.20 (t, 2H)5 3.92 (t, 2H)5 5.00 (br s5 IH)5 5.16 (s, 2H)5 5.86-5.93 (m, 2H)5 6.47 (d, IH)5 6.61 (d, IH), 7.06-7.13 (m, 2H)
Example 184: 1 -[256-dichloro-3-(2-hydroxy-ethylamino)-benzyl]-4-pentyloxy- 1 H- pyridin-2-one
1H NMR (CDCI35 300 MHz) δ 0.91 (t, 3H), 1.32-1.42 (m, 4H)5 1.72-1.79 (m, 2H), 2.54 (t, IH), 3.36 (q, 2H), 3.87-3.94 (m, 4H), 4.84 (t, IH), 5.27 (s, 2H), 5.78 (dd, IH), 5.91 (d, IH)5 6.68-6.71 (m, 2H), 7.23 (d, IH)
Example 185: l-[256-dichloro-3-(2-dimethylamino-ethylamino)-benzyl]-4-pentyloxy- lH-pyridin-2-one 1H NMR (CD3OD5 300 MHz) δ 0.93 (t, 3H), 1.38-1.46 (m, 4H), 1.75-1.80 (m, 2H), 2.55 (s, 6H), 2.91 (t, 2H), 3.46 (t, 2H)5 3.99 (t, 2H), 5.32 (s, 2H)5 5.96 (d, IH)5 6.02 (dd, IH), 6.88 (d, IH)5 6.93 (d, IH)5 7.35 (d, IH)
Example 186: l-[2,6-dichloro-3-(3-hydroxy-propylamino)-benzyl]-4-pentyloxy-lH- pyridin-2-one
1H NMR (CD3OD5 300 MHz) δ 0.93 (t, 3H), 1.38-1.45 (m, 4H)5 1.75-1.90 (m, 4H)5
3.48-3.53 (m, 2H), 3.69 (t, 2H), 3.98 (t, 2H), 5.31 (s, 2H), 5.95 (d, IH), 6.01 (dd, IH),
6.83 (d, IH), 6.90 (d, IH), 7.30 (d, IH)
Example 187: l-[2,6-dichloro-3-(3-dimethylamino-propylamino)-benzyl]-4-pentyloxy- lH-pyridin-2-one
1H NMR (CDCl3 + a few drop of CD3OD, 300 MHz) δ 0.79 (t, 3H)5 1.13-1.30 (m, 4H),
1.61-1.77 (m, 4H)5 2.20 (s, 6H)5 2.38 (t, 2H)5 3.11 (t, 2H)5 3.80 (t, 2H), 5.18 (s, 2H)5 5.76 (dd5 IH)5 5.81 (d, IH)5 6.54 (d, IH), 6.64 (d, IH)5 7,13 (d, IH)
Example 188: l-[3-(3-amino-propylamino)-2,6-dichloro-benzyl]-4-pentyloxy-lH- pyridin-2-one
1H NMR (CD3OD, 300 MHz) δ 0.94 (t, 3H), 1.38-1.46 (m, 4H), 1.75-1.80 (m, 2H), 1.94-2.01 (m, 2H)5 3.01-3.06 (m, 2H), 3.32-3.39 (m. 2H), 3.99 (t, 2H), 5.31 (s, 2H), 5.95 (d, IH)5 6.02 (dd, 1H),6.87 (d, IH)5 6.92 (d, IH)5 7.33 (d, IH)
Example 189: 1 -(3-fluoro-2-methyl-benzyl)-4-pentyloxy-lH-pyridin-2-one
1H NMR (CDCl35 300 MHz) δ 0.93 (t, 3H), 1.32-1.46 (m, 4H), 1.75-1.78 (m, 2H), 2.19 (s, 3H)5 3.93 (t, 2H), 5.08 (s, 2H)5 5.86-5.94 (m, 2H)5 6.82 (d, IH)5 6.92-7.02 (m, 2H)5 7.10-7.15 (m, IH)
Example 190: l-(2-chloro-3-dimethylaminomethyl-4-fluoro-benzyl)-4-pentyloxy-lH- pyridin-2-one
1H NMR (CDCl3, 300 MHz) δ 0.92 (t, 3H)5 1.33-1.45 (m, 4H)5 1.72-1.86 (m, 2H), 3.55 (s5 6H)5 3.91 (t, 2H)5 4.91 (s, 2H)5 5.19 (s, 2H)5 5.88 (d, IH)5 5.98 (dd, IH)5 7.12-7.42 (m, 3H)
Example 191: l-(2,6-dichloro-3-methylamino-benzyl)-4-pentyloxy-lH-pyridin-2-one 1H NMR (CDCl3, 300 MHz) δ 0.92 (t, 3H)5 1.32-1.42 (m, 4H)5 1.75-1.79 (m, 2H), 2.91 (d, 3H)5 3.90 (t, 2H)5 4.49 (q, IH)5 5.33 (s, 2H)5 5.78 (dd, IH)5 5.92 (d, IH)5 6.63 (d, IH)5 6.70 (d, IH)5 7.28 (d, IH)
Example 192: l-(2,6-dichloro-3-dimethylamino-benzyl)-4-pentyloxy-lH-pyridin-2-one 1H NMR (CDCl3, 300 MHz) δ 0.92 (t, 3H)5 1.34-1.41 (m, 4H)5 1.72-1.78 (m, 2H)5 2.80 (s, 6H)5 3.90 (t, 2H), 5.38 (s, 2H)5 5.79 (dd, IH)5 5.93 (d, IH)5 6.69 (d, IH), 7.08 (d, IH)5 7.33 (d, IH)
Example 193: [2-chloro-3-(2-oxo-4-pentyloxy-2H-pyridin-l-ylmethyl)-phenylamino]- acetic acid
1R NMR (DMSOd6, 300 MHz) δ 0.89 (t, 3H), 1.32-1.37 (m, 4H), 1.67-1.71 (m, 2H)5 3.90-3.97 (m. 4H)5 5.03 (s, 2H)5 5.69 (br S5 IH)5 5.83 (s, IH)5 5.99 (d, IH)5 6.05 (d, IH)5 6.52 (d, IH)5 7.05 (t, IH), 7.51 (d, IH) Example 194: l-(6-chloro-benzo[l,3]dioxol-5-ylmethyl)-4-(pyridin-4-ylmethoxy)-lH- pyridin-2-one
1H NMR (CDCl3, 300 MHz) δ 5.02 (s, 2H)5 5.09 (s, 2H), 5.95-6.01 (m, 4H), 6.84 (d, 1H)7.21-7.31 (m, 4H)5 8.62 (d, 2H)
Example 195: 1 -(ό-chloro-benzotl^Jdioxol-S-ylmethyO^-Cό-chloro-pyridin-S- ylmethoxy) -lH-pyridin-2-one
1H NMR (CDCl3, 300 MHz) δ 4.98 (s, 2H)5 5.09 (s5 2H), 5.92-5.99 (m, 4H), 6.83 (d, IH), 7.22-7.40 (m, 3H)5 7.70 (dd, IH)5 8.40 (dd5 IH)
Example 196: l-(6-chloro-benzo[l ,3]dioxol-5-ylmethyl)-4-(4-methoxy-3,5- dimethylpyridin-2-ylmethoxy)-lH-pyridin-2-one
1H NMR (CDCl3, 300 MHz) δ 2.27 (s, 6H), 3.78 (s, 3H)5 5.09 (s5 4H), 6.09-6.10 (m5 4H), 6.84 (s, 2H)5 7.17 (s, IH)5 7.21 (s, IH)5 8.25 (s, IH)
Example 197: l-(6~chloro-benzo[l53]dioxol-5-ylmethyl)-4-(2-methyl-pyridin-3- ylmethoxy)- 1 H-pyridin-2-one
1H NMR (CDCl35 300 MHz) δ 2.58 (s5 3H)5 5.00 (s, 2H)5 5.13 (s, 2H), 5.96-5.98 (m5 3H)5 6.05 (d, IH)5 6.87 (d, 2H)5 7.19 (dd5 IH)5 7.25-7.29 (m5 IH)5 7.67 (d5 IH), 8.51 (d, IH)
Example 198: l-(6-chloro-benzo[l53]dioxol-5-ylmethyl)-4-(thiazol-4-ylmethoxy)-lH- pyridin-2-one 1B. NMR (CDCl3, 300 MHz) δ 5.12 (s, 2H), 5.21 (s, 2H), 5.98 (s, 2H), 6.01 (dd, IH), 6.07 (d, IH)5 6.86 (d, 2H), 7.24 (d, IH), 7.43 (s, IH), 8.87 (s, IH)
Example 199: l-(6-chloro-benzo[l,3]dioxol-5-ylmethyl)-4-(pyridin-2-ylmethoxy)-lH- pyridin-2-one
1H NMR (CDCl3, 300 MHz) δ 5.12 (s, 2H), 5.16 (s, 2H), 5.98 (s5 2H), 6.03-6.05 (m, 2H), 6.86 (d, 2H), 7.25-7.29 (m, 2H), 7.45 (d, IH)5 7.75 (td, IH), 8.63 (d, IH)
Example 200: pentanoic acid l-(6~chloro-benzo[l,3]dioxol-5-ylmethyl)-2-oxo-l,2- dihydro-pyridin-4-yl ester
H NMR (CDCl3, 300 MHz) δ 0.97 (t, 3H)5 1.39-1.47 (m, 2H)5 1.68-1.75 (m, 2H)5 2.54 (t5 2H)5 5.15 (S5 2H)5 5.98 (s, 2H), 6.09 (dd, IH)5 6.38 (d, IH)5 6.86 (s, IH), 6.91 (s, IH)5 7.37 (d, IH)
Example 201: hexanoic acid l-(6-chloro-benzo[l,3]dioxol-5-ylmethyl)-2-oxo-l,2- dihydro-pyridin-4-yl ester
1H NMR (CDCl35 300 MHz) δ 0.93 (t5 3H)5 1.34-1.38 (m5 4H), 1.70-1.76 (m, 2H)5 2.54 (t5 2H)5 5.16 (s5 2H)5 5.98 (s, 2H)5 6.10 (dd, IH), 6.40 (d, IH), 6.87 (s, IH), 6.91 (s, IH), 7.37 (d, IH)
Example 202: 1 -(2-chloro-3-trifluoromethyl-benzyl)-4-pentyloxy-lH-pyridin-2-one 1H NMR (CDCl3, 300 MHz) δ 0.95 (t, 3H)5 1.37-1.45 (m5 4H), 1.78-1.81 (m, 2H), 3.94 (t5 2H)5 5.25 (s, 2H), 5.95-5.98 (m, 2H), 7.19-7.38 (m, 3H), 7.65 (d, IH) Example 203: thiophene-2-carboxyl acid l-(6~chloro-benzo[l,3]dioxol-5-ylmethyl)-2~ oxo- 1 ,2-dihydro-pyridin-4-yl ester
1U NMR (CDCl3, 300 MHz) δ 5.19 (s, 2H), 6.00 (s, 2H), 6.24 (dd, IH), 6.53 (d, IH)5
6.88 (s, IH), 6.94 (s, IH), 7.21 (t, IH), 7.42 (d, IH), 7.72 (d, IH), 7.98 (d, IH)
Example 204: toluene-4-sulfonic acid l-(6-chloro-benzo[l,3]dioxol-5-ylmethyl)-2-oxo-
1 ,2-dihydro-pyridin-4-yl ester
1H NMR (CDCl3, 300 MHz) δ 2.48 (s, 3H), 5.10 (s, 2H), 6.00 (s, 2H), 6.14-6.15 (m,
2H), 6.84 (s, IH), 6.87 (s, IH), 7.34-7.35 (m, IH)5 7.38 (d, 2H)5 7.81 (d, 2H)
Example 205: l-(6-chloro-benzo[l ,3]dioxol-5-ylmethyl)-4~(4,4,555,5-pentafluoro- pentyloxy)- 1 H-pyridin-2-one
1H NMR (CDCl3, 300 MHz) δ 2.08-2.28 (m, 4H), 4.01 (t, 2H), 5.12 (s, 2H)5 5.91-5.93
(m, 2H), 5.98 (s, 2H), 6.84 (s, IH), 6.87 (s, IH), 7.22-7.24 (m, IH)
Example 206: 1 -(6-chloro~benzo[l ,3]dioxol-5-ylmethyl)-4-(2-dimethylamino~ethoxy)-
1 H-pyridin-2-one
1H NMR (CDCl3, 300 MHz) δ 2.33 (s, 6H)5 2.73 (t, 2H), 4.03 (t, 2H)5 5.11 (s, 2H), 5.94-
5.97 (m, 4H), 6.83 (s, IH)5 6.86 (s, IH)5 7.19 (d, IH)
Example 207: 4-chloro-2-(2,4-dichloro~benzyloxy)-pyridine
1H NMR (CDCl3, 300 MHz) δ 5.17 (s, 2H), 6.83 (dd, IH), 6.93 (d, IH), 7.28-7.47 (m,
3H), 8.23 (d, IH) Example 208: 4-chloro-l-(2,4-dichloro-benzyl)-lH-pyridin-2-one
1U NMR (CDCl3, 300 MHz) δ 5,17 (s, 2H), 6.21 (dd, IH), 6.65 (s, IH), 7.22-7.42 (m,
3H), 7.43 (s, IH)
Example 209: l-(2,4-dichloro-benzyl)-4-(5-fluoro-pentyloxy)-lH-pyridin-2-one
1H NMR (CDCl3, 300 MHz) δ 1.58-1.61 (m, 2H), 1.74-1.88 (m, 4H), 3.96 (t, 2H), 4.44 (t, IH), 4.54 (t, IH), 5.16 (s, 2H), 5.93-5.94 (m, 2H), 7.18-7.22 (m, 3H), 7.42 (s, IH)
Example 210: 3-[l-(2,4-dichloro-benzyl)-2-oxo~l,2-dihydro-pyridin-4-yloxymethyl]- indole- 1 -carboxyl acid tetra-butyl ester
1H NMR (CDCl3, 300 MHz) δ 1.61 (s, 9H), 5.18 (s, 2H), 5.40 (s, 2H), 5.95 (dd, IH), 6.15 (d, IH), 7.21-7.60 (m, 7H), 8.23 (d, IH)
Example 211 : 1 -(2,4-dichloro-benzyl)-4-(2-thiophen-2-yl-ethoxy)- 1 H-pyridin-2-one 1H NMR (CDCl3, 300 MHz) δ 3.30 (t, 2H), 4.15 (t, 2H), 5.13 (s, 2H), 5.90-5.97 (m, 2H), 6.87-6.98 (m, 2H), 7.15-7.22 (m, 4H), 7.41 (s, IH)
Example 212: l-(2,4-dichloro-benzyl)-4-(2-thiophen-3-yl-ethoxy)-lH-pyridin-2-one 1H NMR (CDCl3, 300 MHz) δ 3.12 (t, 2H), 4.15 (t, 2H), 5.12 (s, 2H), 5.88-5.97 (m, 2H), 6.95-7.41 (m, 7H)
Example 213: l-(2,4-dichloro-benzyl)-4-(2-pyrrol-l-yl-ethoxy)-lH-pyridin-2-one
1H NMR (CDCl3, 300 MHz) δ 4.18 (t, 2H), 4.28 (t, 2H), 5.14 (s, 2H), 5.82-5.97 (m, 2H),
6.70-6.80 (m, 2H), 7.10-7.25 (m, 3H), 7.40 (s, IH) Example 214: l-(2,4-dichloro-benzyl)-4-(3-pyrrol-l-yl-propoxy)-lH-pyridin-2-one 1H NMR (CDCl3, 300 MHz) δ 2.20 (m, 2H), 3.82 (t, 2H)5 4.03 (t, 2H), 5.14 (s, 2H), 5.86 (d, IH), 5.94 (dd, IH), 6.12-6.18 (m, 2H), 6.60-6.66 (m, 2H), 7.18-7.24 (m, 3H)5 7.40 (s, IH)
Example 215: 1 -(3-amino-2-methyl-benzyl)-4-(2-thiophen-2-yl-ethoxy)-lH-pyridin-2- one
1H NMR (CDCl3, 300 MHz) δ 2.01 (s, 3H), 3.28 (t, 2H), 3.65 (br s, 2H), 4.14 (t, 2H), 5.04 (s, 2H), 5.84 (dd, IH), 5.95 (d, IH), 6.57 (d, IH), 6.70 (d, IH), 6.88-7.02 (m, 4H), 7.16 (dd, IH)
Example 216: 1 -(3-amino-2-methyl-benzyl)-4-(2-pyrrol- 1 -yl-ethoxy)- 1 H-pyridin-2-one 1H NMR (CDCl3, 300 MHz) δ 2.01 (s, 3H), 4.16 (t, 2H), 4.25 (t, 2H), 5.04 (s, 2H), 5.83 (dd, IH), 5.90 (d, IH), 6.16 (t, 2H), 6.57 (d, IH), 6.71-6.75 (m, 3H), 6.91 (d, IH), 7.02 (t, IH)
Example 217: l-(3-amino-2-methyl-benzyl)-4-[2-(4-methyl-thiazol-5-yl)-ethoxy]-lH- pyridin-2-one 1H NMR (CDCl3, 300 MHz) δ 1.98 (s, 3H), 2.40 (s, 3H), 3.20 (t, 2H), 3.46 (br s, 2H), 4.06 (t, 2H), 5.02 (s, 2H), 5.81 (dd, IH), 5.92 (d, IH), 6.53 (d, IH), 6.68 (d, IH), 6.91 (d, IH), 6.99 (t, IH), 8.56 (s, IH)
Example 218: l-(3-Amino-2-methyl-benzyl)-4-(2-(5-bromothiophen-2-yl)-ethoxy)-lH- pyridin-2-one
1H NMR (CDCl3, 300 MHz) δ 1.95 (s, 3H), 3.14 (t, 2H), 3.49 (br s, 2H), 4.05 (t, 2H), 4.99 (s, 2H), 5.81 (dd, IH), 5.88 (m, IH), 6.49 (d, IH), 6.60 (m, IH), 6.64 (d, IH), 6.83 (m, IH), 6.89 (dd, IH), 6.96 (t, IH)
Example 219: l-(3-Amino-2-methyl-benzyl)-4-(2-(5-fluorothiophen-2-yl)-ethoxy)-lH- pyridin-2-one
1H NMR (CDCl3, 300 MHz) δ 2.02 (s, 3H), 3.12 (dt, 2H), 4.09 (t, 2H), 5.05 (s, 2H), 5.85 (dd, IH), 5.93 (d, IH), 6.28 (dd, IH)5 6.46 (d, IH), 6.58 (d, IH), 6.72 (d, IH), 6.92 (d, IH), 7.03 (t, IH)
Example 220: 1 -[3-(2-Hydroxy-ethylamino)-2-methyl-benzyl]-4-(2-thiophen-2-yl- ethoxy)- 1 H-pyridin-2-one
1H NMR (CDCl3, 300 MHz) δ 1.96 (s, 3H), 3.29 (m, 4H), 3.88 (t, 2H), 4.12 (t, 2H)5 5.02 (s, 2H), 5.84 (dd, IH), 5.93 (d, IH), 6.53 (d, IH), 6.66 (d, IH), 6.92 (m, 3H), 7.10 (t, IH), 7.16 (dd, IH)
Example 221: 2-{2-Methyl-3-[2-oxo-4-(2-thiophene-2-yl-ethoxy)-2H-pyridin-l - ylmethyl] -phenylamino } -acetamide 1H NMR (CDCl3, 300 MHz) δ 2.01 (s, 3H), 3.22 (t, 2H), 3.60 (d, 2H), 4.17 (t, 2H), 4.97 (s, 2H), 5.86 (m, IH), 5.94 (dd, IH), 6.20 (d, IH), 6.29 (d, IH), 6.95 (m, 3H), 7.33 (m, 2H)
Example 222: 1 -[3-(Cyclopropylmethyl-amino)-2-methyl-benzyl]-4-(2-thiophen-2-yl- ethoxy)- 1 H-pyridin-2-one
1H NMR (CDCl3, 300 MHz) δ 0.25 (dt, 2H), 0.57 (dt, 2H), 1.06-1.19 (m, IH)3 2.01 (s, 3H), 2.98 (d, 2H), 3.27 (t, 2H), 3.73 (br s, IH), 4.14 (t, 2H)5 5.05 (s, 2H), 5.82 (dd, IH), 5.94 (d, IH), 6.87-6.95 (m, 3H), 7.10 (t, IH)
Example 223: N-{2-Methyl-3-[2-oxo-4-(2-thiophen-2-yl-ethoxy)-2H-pyridin-l- ylmethyl]-phenylamino}-acetonitrile
1H NMR (CDCl3, 300 MHz) δ 2.00 (s, 3H), 3.28 (t, 2H), 4.14 (m, 4H), 5.07 (s, 2H), 5.87 (dd, IH), 5.93 (d, IH), 6.66 (d, IH)5 6.71 (d, IH), 6.93-6.96 (m, 3H), 7.15-7.19 (m, 2H)
Example 224: N-(2-{2-Methyl-3-[2-oxo-4-(2-thiophen-2-yl-ethoxy)-2H-pyridin-l- ylmethyl] -phenylamino } -ethyl)-acetamide
1H NMR (CDCl3, 300 MHz) δ 1.99 (m, 6H), 3.26-3.32 (m, 4H), 3.53-3.59 (m, 2H), 4.14 (t, 2H), 5.05 (s, 2H)5 5.82 (dd, IH), 5.94 (d, IH), 6.52 (d, IH), 6.61(d, IH)5 6.89-6.69 (m, 3H), 7.10 (t, IH), 7.15 (d, IH)
Example 225: l-[2-Methyl-3-(2-pyrrol-l-yl-ethylamino)-benzyl]-4-(2-thiophen-2-yl- ethoxy)- 1 H-pyridin-2-one 1H NMR (CDCl3, 300 MHz) δ 1.85 (s, 3H), 3.28 (t, 2H), 3.51 (t, 3H)5 4.14 (t, 4H), 5.05 (s, 2H), 5.84 (dd, IH), 5.93 (d, IH)5 6.17 (m, 2H), 6.56 (d, IH), 6.65 (m, 3H), 6.90 (m, 3H), 7.10-7.17 (m, 2H)
Example 226: Synthesis of l-[2-Methyl-3-(2-oxo-2-pyrrolidin-l -yl-ethylamino)-benzyl]-4-(2-thiophen-2-yl-ethoxy)-lH-pyridin-2-one
A mixture of {2-Methyl-3-[2-oxo-4-(2-thiophen-2-yl-ethoxy)-2H-pyridin-l- ylmethyl]-phenylamino}-acetic acid(50mg, 0.13mmol), TBTU (60mg, 0.19mmol)5 pyrrolidine (0.02ml, 0.25mmol) and triethylamine (0.09ml, 0.63mmol) was dissolved in jV,iV-dimethylformamide (0.5ml) and stirred at room temperature. After 1 hour, the resulting solution was evaporated, extracted with dichloromethane (20ml) and subjected to silica gel column chromatography (ethyl acetate/MeOH, 20:1) to obtain the titled compound (41mg, 71%).
1H NMR (CDCl3, 300 MHz) δ 1.88-1.95 (m, 2H), 1.99-2.09 (m, 5H), 3.27 (t, 2H), 3.44 (t, 2H), 3.55 (t, 2H), 3.81 (s, 2H), 4.14 (t, 2H), 5.06 (s, 2H), 5.83 (dd, IH), 5.95 (d, IH)5 6.51 (d, IH), 6.54 (d, IH), 6.87-6.94 (m, 3H)5 7.10 (t, IH) 7.16 (dd, IH)
Examples 227 to 230: The procedure of Example 226 was repeated except the starting material to obtain the titled compound.
Example 227: l-[2-Methyl-3-(2-oxo-2-piperidin-l-yl-ethylamino)-benzyl]-4-(2- thiophen-2-yl-ethoxy)- 1 H-pyridin-2-one
1H NMR (CDCl3, 300 MHz) δ 1.53-1.74 (m, 6H), 2.07 (s, 3H), 3.27 (t, 2H), 3.39 (t, 2H),
3.62 (t, 2H), 3.88 (s, 2H), 4.14 (t, 2H), 5.06 (s, 2H), 5.83 (dd, IH), 5.95 (d, IH), 6.52 (d, IH), 6.84-6.96 (m, 3H)5 7.10 (t, IH) 7.16 (dd, IH)
Example 228: N,N-Dimethyl-2- {2-methyl-3-[2-oxo-4-(2-thiophen-2-yl-ethoxy)-2H- pyridin- 1 -ylmethyl]-phenylamino}-acetarnide
1U NMR (CDCl3, 300 MHz) δ 2.08 (s, 3H), 3.05 (s, 6H), 3.28 (t, 2H), 3.88 (s, 2H), 4.15 (t, 2H)5 5.07 (S5 2H)5 5.83 (dd5 IH)5 5.94 (d, IH)5 6.50-6.55 (m, 2H)5 6.89-6.96 (m, 3H), 7.08-7.17 (m, 2H)
Example 229: l-{2-Methyl-3-[2-(4-methyl-piperazin-l-yl)-2-oxo-ethylamino]-benzyl}- 4-(2-thiophen-2-yl-ethoxy)- 1 H-pyridin-2-one
1H NMR (CDCl35 300 MHz) δ 2.07 (s, 3H)5 2.33 (s, 3H)5 2.45 (d, 4H), 3.28 (t, 2H)5 3.48 (d, 2H)5 3.70 (d, 2H)5 3.89 (s, 2H)5 4.14 (t, 2H)5 5.06 (s, 2H)5 5.83 (dd5 IH)5 5.94 (d, IH)5 6.52 (dd, 2H), 6.88-6.97 (m, 3H)5 7.08-7.17 (m, 2H)
Example 230: l-[2-Methyl-3-(2-morpholin-4-yl-2-oxo-ethylamino)-benzyl]-4-(2- thiophen-2-yl-ethoxy)- 1 H-pyridin-2-one
1H NMR (CDCl3, 300 MHz) δ 2.08 (s, 3H), 2.28 (t, 2H)5 3.48 (t, 2H), 3.62-3.79 (m, 6H)5
3.90 (s, 2H), 4.15 (t, 2H)5 5.07 (s, 2H), 5.83 (dd, IH), 5.94 (d, IH)5 6.48 (d, IH)5 6.54 (d,
IH), 6.88-6.96 (m, 3H)5 7.08-7.18 (m, 2H)
Examples 231 to 266: The procedure of Example 1 was repeated except the starting material to obtain the titled compound.
Example 231 : 1 -(3 - Amino-2-methyl-benzyl)-4-(2-furan-2-yl-ethoxy)- 1 H-pyridin-2-one 1U NMR (CDCl3, 300 MHz) δ 2.01 (s, 3H), 3.10 (t, 2H), 4.17 (t, 2H), 5.05 (s, 2H)5 5.81 (dd, IH), 5.95 (d, IH), 6.10 (d, IH)5 6.30 (d, IH), 6.57 (d, IH)5 6.69 (d, IH), 6.90 (d, IH)5 7.02(t, IH)5 7.29 (d, IH)
Example 232: l-(3-Amino-2-methyl-benzyl)-4-[2-(5-methyl-thiophen-2-yl)-ethoxy]- lH-pyridin-2-one
1H NMR (CD3OD, 300 MHz) δ 2.02(s, 3H), 2.40 (s, 3H), 3.19 (t, 2H), 4.16 (t, 2H), 5.07(s, 2H), 5.96 (d, IH), 6.06 (dd, IH), 6.40 (d, IH), 6.57 (dd, IH), 6.67 (d, IH)5 6.73 (d, IH), 6.95 (t, IH), 7.21 (d, IH)
Example 233: 1 -(3-Amino-2-methyl-benzyl)-4-[2-(5-chloro-thiophen-2-yl)-ethoxy]- lH-pyridin-2-one
1H NMR (CDCl3, 300 MHz) δ 2.01(s, 3H), 3.18 (t, 2H), 3.70 (br s, 2H), 4.10 (t, 2H)5 5.05 (s, 2H), 5.84 (dd, IH), 2.92 (d, IH), 6.57 (d, IH), 6.65 (d, IH), 6.69 (d, IH), 6.74 (d, IH), 6.92 (d, IH), 7.02 (t, IH)
Example 234: l-(2,4-dichloro-benzyl)-4-[2-(3-methyl-thiophen-2-yl)-ethoxy]-lH- pyridin-2-one
1H NMR (CDCl3, 300 MHz) δ 2.20(s, 3H), 3.20 (t, 2H), 4.10 (t, 2H), 5.14 (s, 2H), 5.93- 5.97 (m, 2H), 6.80 (d, IH)5 7.07 (d, IH)5 7.17-7,20 (m, 3H), 7.40 (s, IH)
Example 235 : 1 -(3 - Amino-2-methyl-benzyl)-4-(2-benzo [b]thiophen-3-yl-ethoxy)- 1 H- pyridin-2-one
1H NMR (CD3OD, 300 MHz) δ 2.00 (s, 3H), 3.31 (t, 2H)5 4.31 (t, 2H), 5.04 (s, 2H)5 5.96-6.01 (m, 2H), 6.37 (d, IH), 6.72 (d, IH)5 6.93 (t, IH)5 7.14-7.42 (m, 5H)5 7.84 (t, IH)
Example 236: 1 -(3-Amino-2-methyl-benzyl)-4-[2-(5-chloro-3-methyl- benzo [b]thiophen-2-yl)-ethoxy] - 1 H-pyridin-2-one 1H NMR (CD3OD + a few drop of CDCl3, 300 MHz) δ 1.97 (s, 3H), 2.32 (s, 3H), 3.32 (t, 2H), 4.20 (t, 2H), 5.01 (s, 2H), 5.92-5.97 (m, 2H), 6.45 (d, IH), 6.71 (d, IH), 6.96 (t, IH), 7.02 (d, IH), 7.21 (dd, IH), 7.55 (d, IH), 7.65 (d, IH)
Example 237: l-(3-amino-2-methyl-benzyl)-4-[2-(3-methyl-benzo[b]thiophen-2-yl)- ethoxy]-lH-pyridin-2-one
1H NMR (CDCl3, 300 MHz) δ 2.00(s, 3H), 2.36 (s, 3H), 3.33 (t, 2H), 3.73 (br s, 2H),
4.18 (t, 2H), 5.05 (s, 2H), 5.82 (dd, IH), 5.95 (d, IH), 6.56 (d, IH), 6.69 (d, IH), 6.91 (d,
IH), 7.02 (t, IH), 7.27-7.39 (m, 2H), 7.63 (d, IH)5 7.77 (d, IH)
Example 238: l-(3-Amino-2-methyl-benzyl)-4-[2-(5-methyl-furan-2-yl)-ethoxy]-lH- pyridin-2-one
1H NMR (CDCl3, 300 MHz) δ 2.00 (s, 3H), 2.24 (s, 3H), 3.03 (t, 2H), 4.13 (t, 2H), 5.03
(s, 2H), 5.80-5.86 (m, 2H), 5.94-5.96 (m, 2H), 6.53 (d, IH), 6.66 (d, IH), 6.89 (d, IH), 7.00(t, IH)
Example 239 : 1 -(3-Amino-2-methyl-benzyl)-4- [2-(5-ethyl-furan-2-yl)-ethoxy] - 1 H- pyridin-2-one
1H NMR (CDCl3, 300 MHz) δ 1.20 (t, 3H), 1.99 (s, 3H), 2.59 (q, 2H), 3.04 (t, 2H), 3.68 (br s, 2H), 4.14 (t, 2H), 5.04 (s, 2H), 5.80 (dd, IH), 5.86 (d, IH), 5.94 (d, IH), 5.97 (d, IH), 6.55 (d, IH), 6.67 (d, IH), 6.89 (d, IH), 7.00 (t, IH)
Example 240: 5-[l -(3-amino-2-methyl-benzyl)-2-oxo-l ,2-dihydro-pyridin-4- yloxymethyl]-furan-2-carboxylic acid ethyl ester 1H NMR (CDCl3, 300 MHz) δ 1.37 (t, 3H)5 2.00 (s, 3H)5 4.36 (q, 2H)5 4.97 (s, 2H), 5.05 (S5 2H)5 5.84 (dd5 IH)5 6.01 (d, IH)5 6.55-6.58 (m, 2H), 6.69 (d, IH)5 6.93 (d, IH)5 7.02 (UH). 7.14 (d, IH)
Example 241: l-[3-(2-dimethylamino-ethylamino)-2-methyl-benzyl]-4-(2-thiophen-2- yl-ethoxy)- 1 H-pyridin-2 -one
1H NMR (CDCl3, 300 MHz) δ 1.99 (s, 3H), 2.30 (s, 6H)5 2.60 (t, 2H), 3.17 (t, 2H), 3.28
(t, 2H)5 4.14 (t, 2H), 5.06 (s, 2H), 5.83 (dd, IH)5 5.94 (d, IH)5 6.88-6.96 (m, 3H)5 7.09-
7.18 (m, 2H)
Example 242: l-(3-amino-2-methyl-benzyl)-4-[2-(5-methylsulfanyl-thiophen-2-yl)- ethoxy] - 1 H-pyridin-2-one
1H NMR (CDCl3, 300 MHz) δ 2.01 (s, 3H)5 2.45 (s, 3H)5 3.21 (t, 2H), 3.70 (br s, 2H),
4.12 (t, 2H), 5.05 (s, 2H), 5.84 (dd, IH), 5.93 (d, IH), 6.57 (d, IH), 6.69-6.73 (m, 2H), 6.91-6.93 (m, 2H)5 7.02 (t, IH)
Example 243: l-(3-amino-2-methyl-benzyl)-4-(2-benzoftιran-2-yl-ethoxy)-l H-pyridin- 2-one
1H NMR (CDCl3, 300 MHz) δ 2.05 (s, 3H)5 3.25 (t5 2H)5 4.29 (t, 2H)5 5.05 (s, 2H)5 5.82 (d, IH)5 6.00 (s, IH), 6.51-6.71 (m, 3H)5 6.91 (d, IH)5 7.04 (t, IH)5 7.17-7.28 (m, 2H), 7.42 (d, IH), 7.50 (d, IH)
Example 244: 1 -(3-amino-2-methyl-benzyl)-4-[2-(3-methyl-isoxazol-5-yl)-ethoxy]-lH- pyridin-2-one 1H NMR (CDCl3 +a few drop of CD3OD, 300 MHz) δ 1.86 (s, 3H), 1.93 (s, 3H), 2.63 (t, 2H), 4.14 (t, 2H), 4.96 (s, 2H), 5.82 (dd, IH), 5.90 (d, IH), 6.46 (d, IH), 6.64 (d, IH), 6.86 (d, IH), 6.94 (t, IH), 7.26 (s, IH)
Example 245: l-(3-amino-2-methyl-benzyl)-4-[2-(4,5-dimethyl-thiophen-2-yl)- ethoxy]- 1 H-pyridin-2-one
1H NMR (CDCl3, 300 MHz) δ 2.00 (s, 3H), 2.07 (s, 3H)5 2.78 (s, 3H), 3.14 (t, 2H), 4.09
(t, 2H), 5.05 (s, 2H), 5.85 (dd, IH), 5.95 (d, IH), 6.55 (s, IH), 6.56 (d, IH), 6.69 (d, IH),
6.91 (d, IH), 7.01 (t, IH)
Example 246: l-(3-amino-2-methyl-benzyl)-4-[2-(5-ethyl-thiophen-2-yl)-ethoxy]-lH- pyridin-2-one
1H NMR (CDCl3, 300 MHz) δ 1.28 (t, 3H), 2.00 (s, 3H), 2.78 (q, 2H), 3.20 (t, 2H), 3.69
(br s, 2H), 4.11 (t, 2H), 5.04 (s, 2H), 5.84 (dd, IH), 5.94 (d, IH), 6.55-6.70 (m, 4H), 6.91 (d, IH), 7.01 (t, IH)
Example 247: 1 -(3-amino-2,6-dichloro-benzyl)-4-(2-thiophen-2-yl-ethoxy)- 1 H- pyridin-2-one
1H NMR (CDCl3, 300 MHz) δ 3.25 (t, 2H), 4.12 (t, 2H), 4.30 (br s, 2H), 5.30 (s, 2H), 5.81 (dd, IH), 5.92 (d, IH), 6.70-6.93 (m, 4H), 7.13-7.16 (m, 2H)
Example 248: N-{2-methyl-3-[2-oxo-4-(2-thiophen-2-yl-ethoxy)-2H-pyridin-l - y lmethy 1] -phenyl } -acetamide
1R NMR (DMSO-tftf, 300 MHz) δ 2.02 (s, 3H), 2.08 (s, 3H), 3.22 (t, 2H), 4.17 (t, 2H), 5.00 (s, 2H), 5.87 (d, IH), 5.99 (dd, IH), 6.57 (d, IH)5 6.94-6.96 (m, 2H), 7.07 (t, IH), 7.19 (d, IH), 7.32-7.34 (m, IH), 7.43 (d, IH)
Example 249: l-[2-methyl-3-(2-piperidin-l -yl-ethylamino)-benzyl]-4-(2-thiophen-2-yl- ethoxy)-lH-pyridin-2-one
1H NMR (CDCl3, 300 MHz) δ 1.59 (br s, 2H), 1.83-1.87 (m, 4H), 2.07 (s, 3H), 2.90- 2.94 (m, 4H), 3.06 (t, 2H), 3.28 (t, 2H), 3.52 (t, 2H), 4.13 (t, 2H)3 4.60 (br s, IH), 5.03 (s, 2H), 5.86 (dd, IH), 5.92 (d, IH), 6.46 (d, IH), 6.59 (d, IH), 6.88-6.96 (m, 3H), 7.07 (t, IH), 7.16 (dd, IH)
Example 250: 1 -[2-methyl-3-(2-morpholin-4-yl-ethylamino)-benzyl]-4-(2-thiophen-2- yl-ethoxy)- lH-pyridin-2-one
1H NMR (CDCl3, 300 MHz) δ 2.00 (s, 3H), 2.47 (t, 4H), 2.69 (t, 2H), 3.18 (t, 2H), 3.28 (t, 2H), 3.70 (t, 4H), 4.14 (t, 2H), 5.06 (s, 2H), 5.83 (dd, IH), 5.94 (d, IH), 6.53 (d, IH), 6.61 (d, IH), 6.88-6.95 (m, 3H), 7.10 (d, IH), 7.15 (t, IH)
Example 251: N-{2-methyl-3-[2-oxo-4-(2-thiophen-2-yl-ethoxy)-2H-pyridin-l- ylmethyl] -phenyl} -methanesulfonamide
1H NMR (CDCl3, 300 MHz) δ 2.15 (s, 3H), 2.95 (s, 3H), 3.30 (t, 2H), 4.17 (t, 2H), 5.01 (s, 2H), 5.97 (dd, 2H), 6.03 (d, IH), 6.74 (d, IH), 6.89-6.96 (m, 2H), 7.01 (d, IH), 7.09 (t, IH), 7.16 (dd, IH), 7.28 (t, IH), 7.60 (br s, IH)
Example 252: 1 -(3-amino-2-methyl-benzyl)-4-[2-(4-bromo-thiophen-2-yl)-ethoxy]-lH- pyridin-2-one 1H NMR (CDCl3, 300 MHz) δ 1.99 (s, 3H)5 3.22 (t, 2H)5 3.69 (br S5 2H)5 4.10 (t, 2H), 5.04 (S5 2H)5 5.83 (dd, IH)5 5.92 (d, IH)5 6.55 (d, IH)5 6.68 (d, IH), 6.80 (s, IH), 6.91 (d, IH), 6.98-7.06 (m, 2H)
Example 253: l-(6-chloro-benzo[l,3]dioxol-5-ylmethyl)-4-(2-pyrrol-l-yl-ethoxy)-lH- pyridin-2-one
1H NMR (CDCl3, 300 MHz) δ 4.15 (t, 2H), 4.25 (t, 2H), 5.07 (s, 2H), 5.85-5.90 (m, 2H),
5.94 (s, 2H), 6.15-6.16 (m, 2H), 6.60-6.72 (m, 2H)5 6.79 (s, IH), 6.83 (s, IH), 7.18 (d,
IH)
Example 254: 1 -(6-chloro-benzo[l ,3]dioxol-5-ylmethyl)-4-(2-thiophen-2-yl-ethoxy)- lH-pyridin-2-one
1H NMR (CDCl3, 300 MHz) δ 3.26 (t, 2H), 4.12 (t, 2H)5 5.06 (s, 2H)5 5.89-5.92 (m, 4H)5
6.78-6.94 (m, 4H), 7.14-7.18 (m, 2H)
Example 255: 1 -[2-methyl-3-(2-pyrrolidin- 1 -yl-ethylamino)-benzyl]-4-(2-thiophen-2- yl-ethoxy)- 1 H-pyridin-2-one
1H NMR (CDCl35 300 MHz) δ 1.78 (br s, 4H), 1.98 (s, 3H), 2.55 (br s, 4H)5 2.79 (t, 2H)5
3.23 (t, 2H)5 3.28 (t, 2H), 4.14 (t, 2H), 4.33 (br s, IH), 5.05 (s, 2H), 5.81-5.85 (m, IH), 5.94 (d, IH)5 6.53 (d, IH)5 6.63 (d, IH), 6.88-6.96 (m, 3H)5 7.09-7.18 (m, 2H)
Example 256: N-(2-{2-methyl-3-[2-oxo-4-(2-thiophen-2-yl-ethoxy)-2H-pyridin-l- y lmethyl] -phenylamino } -ethyl)-acetamide
1HNMR (CDCl3, 300 MHz) δ 1.94 (s, 6H), 3.25 (t, 4H), 3.49 (q, 2H), 4.10 (t, 2H), 5.00 (s, 2H)5 5.83-5.89 (m, 2H), 6.44 (d, IH), 6.58 (d, IH), 6.73 (t, IH), 6.87-6.94 (m, 3H), 7.06 (t, IH), 7.14 (d, IH)
Example 257: l-{2-methyl-3-[(pyridin-3-ylmethyl)-amino]-benzyl}-4-(2-thiophen-2- yl-ethoxy)-lH-pyridin-2-one
1H NMR (CDCl3, 300 MHz) δ 2.03 (s, 3H), 3.28 (t, 2H), 4.14 (t, 2H), 4.42 (s, 2H)3 5.07 (s, 2H), 5.86 (dd, IH), 5.93 (d, IH), 6.56 (d, 2H), 6.88-6.96 (m, 3H), 7.07 (t, IH), 7.16 (dd, IH), 7.30-7.34 (m, IH), 7.73 (d, IH), 8.54 (s, IH), 8.64 (s, IH)
Example 258: 2-methyl-3-[2-oxo-4-(2-thiophen-2-yl-ethoxy)-2H-pyridin-l-ylmethyl]- phenyl ester
1H NMR (CDCl3, 300 MHz) δ 2.26 (s, 3H), 3.16 (s, 3H), 3.27 (t, 2H), 4.14 (t, 2H), 5.06 (s, 2H), 5.93-5.95 (m, 2H), 6.88-7.00 (m, 4H), 7.14-7.26 (m, 3H)
Example 259: l-{2-methyl-3-[(pyridin-4-ylmethyl)-amino]-benzyl}-4-(2-thiophen-2- yl-ethoxy)- lH-pyridin-2-one
1H NMR (CDCl3, 300 MHz) δ 2.07 (s, 3H), 3.28 (t, 2H), 4.14 (t, 2H), 4.44 (s, 2H), 5.08
(s, 2H), 5.86 (dd, IH), 5.94 (d, IH), 6.42 (d, 2H), 6.54 (d, IH), 6.88-7.11 (m, 4H), 7.16
(dd, IH), 7.30 (d, 2H), 8.55 (d, 2H)
Example 260: l-{2-methyl-3-[(thiazol-4-ylmethyl)-amino]-benzyl}-4-(2-thiophen-2-yl- ethoxy)- 1 H-pyridin-2-one
1H NMR (CDCl3, 300 MHz) δ 2.04 (s, 3H), 3.28 (t, 2H), 4.14 (t, 2H), 4.56 (s, 2H), 5.06
(s, 2H), 5.84 (dd, IH)5 5.94 (d, IH), 6.55 (d, IH), 6.65 (d, IH), 6.88-7.20 (m, 6H)5 8.85 (S, IH)
Example 261 : 1 -[3-(4-methoxy-benzyloxy)-2-methyl-benzyl]-4-(2~thiophen-2-yl~ ethoxy)- 1 H-pyridin-2-one 1H NMR (CDCl3, 300 MHz) δ 2.15 (s, 3H), 3.29 (t, 2H), 3.81 (s, 3H), 4.16 (t, 2H), 4.99 (s, 2H), 5.08 (s, 2H), 5.88 (dd, IH), 6.00 (d, IH), 6.68 (d, IH), 6.90-6.96 (m, 6H), 7.11- 7.18 (m, 2H), 7.35 (d, 2H)
Example 262: 1 -{3-[(3.5-dimethyl-isoxazol-4-ylmethyl)-amino]-2-methyl-benzyl}-4- (2-thiophen-2-yl-ethoxy)- 1 H-pyridin-2-one
1H NMR (CDCl3, 300 MHz) δ 1.98 (s, 3H), 2.26 (s, 3H), 2.37 (s, 3H), 3.28 (t, 2H), 4.04 (s, 2H), 4.15 (t, 2H), 5.07 (s, 2H), 5.85-5.95 (m, 2H), 6.62 (d, IH), 6.74 (d, IH), 6.88- 6.96 (m, 3H), 7.14-7.19 (m, 2H)
Example 263: l-(3-hydroxy-2-methyl-benzyl)-4-(2-thiophen-2-yl-ethoxy)-l H-pyridin- 2-one
1H NMR (CDCl3 + a few drop Of CD3OD, 300 MHz) δ 1.96 (s, 3H), 3.16 (t, 2H), 4.05 (t, 2H), 4.91 (s, 2H), 5.85-5.88 (m, 2H), 6.41 (d, IH), 6.66 (d, IH), 6.76-6.90 (m, 4H), 7.04 (d, IH)
Example 264: l-{2-methyl-3-[(l-methyl-pyrrolidin-2-ylmethyl)-amino]-benzyl}-4-(2- thiophen-2-yl-ethoxy)- 1 H-pyridin-2-one
1H NMR (CDCl3 + a few drop of CD3OD, 300 MHz) δ 1.57-1.67 (m, 3H), 1.79-1.89 (m, 6H), 2.25 (s, 3H), 2.47-2.50 (m, IH), 2.98-3.04 (m, 2H), 3.13 (t, 2H), 4.01 (t, 2H), 4.88 (S5 2H), 5.78-5.81 (m, 2H), 6.32 (d, IH), 6.47 (d, IH), 6.73-6.85 (m, 3H), 6.94 (t, IH), 7.00 (d, IH)
Example 265: l-{2-methyl-3-[2-(l-methyl-pyrrolidin-2-yl)-ethylamino]-benzyl}-4-(2- thiophen-2-yl-ethoxy)- 1 H-pyridin-2-one
1H NMR (CDCl3, 300 MHz) δ 1.67-1.79 (m, 3H), 1.90-1.98 (m, 6H)5 2.24 (q, 2H), 2.40 (s, 3H)5 3.10-3.30 (m, 5H), 4.14 (t, 2H)5 4.88 (br s, IH)5 5.04 (s, 2H)5 5.82 (dd, IH), 5.93 (d, IH)5 6.52 (d, IH), 6.60 (d, IH), 6.88-6.96 (m, 3H), 7.08-7.17 (m, 2H)
Example 266: (2-{2-methyl-3-[2-oxo-4-(2-thiophen-2-yl-ethoxy)-2H-pyridin-l- ylmethyl]-phenylamino}-ethyl)-phosphonic acid diethyl ester
1H NMR (CDCl3, 300 MHz) δ 1.32 (t, 6H)5 2.02 (s, 3H)5 2.10-2.20 (m, 2H)5 3.28 (t, 2H)5 3.42-3.53 (m, 2H), 4.07-4.17 (m. 6H)5 5.06 (s, 2H), 5.85 (dd, IH)5 5.96 (s, IH)5 6.57 (d, IH), 6.68 (d, IH), 6.88-6.96 (m, 3H), 7.10-7.17 (m, 2H) Preparation of 4-(isobutylthio)pyridine 1-oxide: A solution of 5.80g of isobutylthiol in 30ml of DMF was stirred at room temperature and 2.55g of NaOMe was added. After 30mins 6.Og of N-oxide was added and the reaction mixture was heated at reflux for 15 hours. The mixture was cooled, then solution was evaporated, extracted with dichloromethane and subjected to silica gel column chromatography(hexane/ethyl acetate) to obtain 5.8g of 4-(isobutylthio)pyridine 1-oxide
1H NMR (CDCl3, 300 MHz) δ 0.99(s, 3H), 1.01(s, 3H), 1.85-1.89(m, IH), 2.78(d, J=6.9Hz, 2H), 7.04(d, J=7.2Hz, 2H)5 8.01 (d, J=7.5Hz, 2H)
Preparation of 4-(isobutylthio)pyridine-2(lJϊ)-one: A mixture of 500mg of 4-(isobutylthio)pyridine-N-oxide , 5ml of acetic anhydride was heated at reflux for 10 hours. The mixture was cooled, then added MeOH and 3N NaOH was added dropwise at pH 9~11 and stirred. After 1 hour solution was evaporated and 3N HCl was added dropwise at pH6.5~7.5, extracted with ethyl acetate and subjected to silica gel column chromatography(hexane/ethyl acetate) to obtain the compound (90mg).
1H NMR (CDCl3, 300 MHz) δ 1.05(s, 3H)5 1.07(s, 3H)5 1.95-2.00(m, IH), 2.79(d, J=6.9Hz, 2H), 6.19(dd, IH), 6.3 l(s, IH)5 7.21(d, J=6.9Hz, IH)
Example 267: 4-(isobutylthio)- 1 -(2-methyl-3-nitrobenzyl)pyridin-2(l H)-one Preparation of 4-(isobutylthio)-l-(2-methyl-3-nitrobenzyl)pyridine-2(l/2')- one: A mixture of lOOmg of 4-(isobutylthio)pyridine-2(lH)-one, 2ml of DMF, 65mg of t-BuOK was stirred at room temperature and 105mg of 2-methyl~3-nitrobenzyl chloride was added. After 3 hour, the resulting solution was evaporated, extracted with dichloromethane and subjected to silica gel column chromatography(hexane/ethyl acetate) to obtain the compound (90mg).
1H NMR (CDCl3, 300 MHz) δ 1.06(s, 3H), 1.08(s, 3H), 1.94-2.03(m, IH), 2.42(s, 3H), 2.80(, J=6.9Hz, 2H), 5.15(s5 2H), 6.07(dd, IH), 6.35(s, IH), 6.93(, J=7.5Hz, IH)5 7.19- 7.33(m, 2H), 7.71(, J=8.1Hz, IH)
Examples 268 to 280: The procedure of Example 267 was repeated except the starting material to obtain the titled compound.
Example 268: l-(3-amino-2-methylbenzyl)-4-(isobutylthio)pyridin-2(lH)-one A mixture of 400mg of l-(3~amino-2-methylbenzyl)-4-(isobuthylthio)pyridin-
2(lH)-one, 5ml of ethyl alcohol, 3ml of Raney nickel in water was stirred at room temperature and 3.5ml Of NH2NH2H2O was added dropwise. After 1 hour, the catalyst was removed by filtration through Celite, and resulting solution was evaporated, extracted with dichloromethane to obtain the title compound (200mg).
1H NMR (CDCl3, 300 MHz) δ 1.01-1.07(m. 6H), 1.95-1.99(m, IH), 2.13(s, 3H), 2.77(d, J=6.9Hz, 2H), 5.07(s, 2H), 5.97(dd, IH), 6.32(s, IH)5 6.70(d, J=7.8Hz, IH), 6.85- 6.92(m, 2H), 7.08(t, J=7.8Hz, IH)
Example 269 : 1 -(3 -amino-2-methylbenzyl)-4-(furan-2-ylmethylthio)pyridine-2( 1 H)- one
1H NMR (CDCl3, 300 MHz) δ 2.03(s,3H), 4.14(s,2H), 5.05(s,2H), 5.96(dd, IH), 6.31(s, 2H), 6.45(d, J=7.8Hz, IH), 6.76(d5 J=7.5Hz, IH), 6.88(d, J=6.9Hz, IH), 7.04(t, J=7.8Hz, IH), 7.36(s, IH)
Example 270: l-(3-amino-2-methylbenzyl)-4-(pentylthio)pyridine-2-(lH)-one
1H NMR (CDCl3, 300 MHz) δ 0.89-0.93(m, 3H), 1.31-1.44(m, 4H), 1.66-1.73(m, 2H), 2.03(s, 3H), 2.85-2.90(m, 2H), 5.05(s, 2H), 5.92-5.95(m, IH), 6.33(s, IH), 6.60(d, J=7.2Hz, IH), 6.73(d, J=7.8Hz, IH), 6.85(q, IH), 7.03(t, J=7.8Hz, IH)
Example 271: l-(3-amino-2-methylbenzyl)-4-(phenethylthio)pyridine-2(lH)-one
1H NMR (CDCl3, 300 MHz) δ 2.13(s, 3H), 3.00(t, J=7.5Hz, 2H), 3.16(t, J=7.5Hz, 2H)5 5.06(s, 2H), 5.94-5.97(dd, IH), 6.39(s, IH), 6.66(bs, IH), 6.88(d, J=7.5Hz, 2H), 7.06- 7.10(m, IH), 7.19-7.35(m, 3H) Example 272: l-(3-amino-2-methylbenzyl)-4-(butylthio)pyridine-2(lH)-one 1K NMR (CDCl35 300 MHz) δ 0.95(t, J=7.2Hz, 3H)5 1.43-1.50(m,2H), 1.67-1.72(m,2H), 2.04(s5 3H)5 2.89(t, J=7.3Hz, 2H)5 5.05(s, 2H)5 5.94(dd, IH)5 6.33(s, IH)5 6.61 (d, J=7.6Hz5 IH)5 6.75(d, J=8.1Hz5 IH)5 6.86(d5 J=7.2Hz5 IH)5 7.04(t5 J=7.6Hz, IH)
Example 273: 1 -(3-amino-2-methylbenzyl)-4-(thiophen-2-ylmethylthio)pyridine- 2(l#)-one
1H NMR (CDCl3, 300 MHz) δ 2.03(s, 3H)5 4.34(s,2H), 5.04(s, 2H), 5.95(dd, IH)5 6.41(bs5 IH)5 6.60(d, J=7.5Hz, IH), 6.75(d, J=7.5Hz, IH)5 6.87-6.95(m5 2H)5 7.01- 7.05(m, 2H), 7.21 -7.26(m, IH)
Example 274: 1 -(3-amino-2-methylbenzyl)-4-(pentylthio)pyridine-2(lH)-one 1H NMR (CDCl3, 300 MHz) δ 0.92(t, J=6.8Hz, 3H)5 1.32-1.46(m5 4H)5 1.68-1.78(m, 2H)5 2.43(s, 3H)5 2.91(t5 J=7.3Hz, 2H)5 5.15(s, 2H)5 6.07(dd, IH)5 6.38-6.39(m, IH)5 6.94(d, J=7.2Hz, IH)5 7.20-7.31(m, 2H)5 7.72(d, J=8.1Hz, 2H)
Example 275: l-(3-amino-2-methylbenzyl)-4-(propylthio)pyridine-2(lH)-one 1H NMR (CDCl3, 300 MHz) δ 1.05(t, J=7.5Hz, 3H)5 1.71-1.78(m, 2H)5 2.02(s5 3H), 2.87(t, J=7.3Hz, 2H)5 5.06(s, 2H)5 5.94(dd5 IH)5 6.33(d5 J=I.8Hz5 IH)5 6.59(d5 J=7.8Hz, IH)5 6.70(d, J=7.5Hz5 IH)5 6.86(d, J-7.2Hz, IH)5 7.03 (t, J=7.8Hz, IH)
Example 276: l-(3-amino-2-methylbenzyl)-4-(l-methylbutylthio)pyridine-2(lH)-one 1H NMR (CDCl3, 300 MHz) δ 0.93-1.02(m, 6H), 1.55-1.62(m, 2H), 1.68-1.75(m, IH)5 2.06(S5 3H)5 2.89(t, J=7.5Hz5 2H), 5.06(s, 2H), 5.94(dd, IH), 6.33(s5 IH), 6.63(d, J=7.2Hz, IH)5 6.78(d, J=8.1Hz, IH)5 6.86(d5 J=7.2Hz5 IH)5 7.04(t, J=7.6Hz5 IH)
Example 277: N5N-dimethyl-3-(2-methyl-3-((2-oxo-4-(2-(thiophen-2- yl)ethoxy)pyridin- 1 (2H)-yl)methyl)phenylamino)propane- 1 -sulfonamide 1H NMR (CDCl3, 300 MHz) δ 2.06(s, 3H)5 2.23(t, J=6.8Hz5 2H), 2.87(s, 6H), 3.06(t, J=7.2Hz, 2H)5 3.29(t3 J=6.5Hz, 2H), 3.39(t, J=6.7Hz, 2H)5 3.62-3.68(m5 IH)5 4.14- 4.18(m, 2H)5 5.06(s, 2H), 5.87(dd, IH), 5.97(d, J=2.1Hz, IH), 6.60(d, J=7.5Hz, IH)5 6.80(bs, IH), 6.90(bs, IH), 6.93-6.96(m5 2H), 7.10-7.18(m, 2H)
Example 278: l-(3-nitro-2-methylbenzyl)-4-chloropyridin-2(lH)-one
1H NMR (CDCl3, 300 MHz) δ 2.38(s, 3H), 5.38(s, 2H)5 6.54(dd5 IH)5 7.27(d5 J=7.8Hz, IH), 7.45(t, J=7.9Hz5 IH), 7.79(d5 J=7.8Hz5 2H), 8.21(s, IH)
Example 279: l-(3-amino-2-methylbenzyl)-4-chloropyridin-2(lH)-one 1H NMR (CDCl3, 300 MHz) δ 1.94(s, 3H)5 5.08(s, 2H), 6.23-6.28(m, 2H)5 6.63(d5 J=7.8Hz, IH)5 6.90(t, J=7.8Hz, IH), 8.1 l(s, IH)
Example 280: 1 -(3-amino-2-methylbenzyl)-4-(2-(thiophene-2-yl)ethylamino)pyridine- 2-(l#)-one 1U NMR (CDCl3, 300 MHz) δ 2.02(s, 3H), 3.07(t, J=6.8Hz, 2H), 3.37(t, J=6.5Hz5 2H)5 4.97(s, 2H)5 5.64(d, J=8.1Hz5 2H), 6.55(d5 J=7.5Hz5 IH)5 6.75-6.83(m5 3H), 6.88- 6.91(m, IH)5 7.00(t5 J=7.5Hz, IH)5 7.12(d, J=5.1Hz, IH) Test Example 1: Minimum Inhibitory Concentration (MIC)
Antibacterial activities of the compounds synthesized in the Examples were assessed by measuring their MIC values for standard strains. Specifically, MIC value was measured by conducting the following steps: diluting a test compound according to a two-fold dilution method; dispersing the resulting dilution in a Mϋller-Hinton agar broth; inoculating 2 ml of the standard strain culture having a concentration of 107 cfu(colony forming unit)/ml; and incubating the mixture for 20 hrs at 37°C. The resulting MIC values were in the range of 128 to 0.2 μg/ml, preferably, 1 to 0.2 μg/ml.
These results reveal that the compounds of the present invention have superior antibacterial activity against various infectious bacterial strains including MRSA strain.

Claims

WHAT IS CLAIMED IS:
1. A compound having a formula selected from the group consisting of formula (I), formula (II), and pharmaceutically acceptable analogs thereof selected from the group consisting of salt, acid, ester, amide, and nitrile:
Figure imgf000094_0001
Figure imgf000094_0002
wherein,
R1 is selected from the group of radicals consisting of:
(a) H5
(b) C1-8 alkyl, C1-8 alkenyl, C1-8 alkynyl,
(c) aryl, C3-8 cycloalkyl, C3-8 cycloalkenyl, (d) an analog of a radical of group (c) containing one or more heteroatoms selected from N, S and O, and
(e) a substituted analog of a radical selected from the group consisting of groups (b), (c), and (d), said substituted analog containingone or more substituents selected from the group consisting of: hydroxyl., halogen, Ci-6 alkyl, C3-S cycloalkyl, C3-8 heterocycloalkyl, alkyloxy, amino, alkylamino, carboxyl, nitro, sulfonylamide, alkylsulfonyl, amide, dioxoisoindole, trihaloalkyl, aryl, heteroaryl, substituted aryl, and substituted heteroaryl, wherein said substituted aryl and substituted heteroaryl contain one or more substituents selected from the group consisting of C1-6 alkyl, C3-8 cycloalkyl, C3-8 heterocycloalkyl, alkyloxy, amino, alkylamino, carboxyl, nitro, sulfonylamide, alkylsulfonyl, amide, dioxoisoindole, trihaloalkyl, and aryl;
A is selected from the group consisting of C-R2 and N;
R2 is selected from the group consisting of H, C1-5 alkyl, benzyl, and substituted C1-5 alkyl containing one or more substituents selected from the group consisting of methyl, ethyl, hydroxyl, hydroxylmethyl and hydroxylethyl; B is selected from the group consisting of carbonyl, CH2 and NH;
R4 is selected from the group of radicals consisting of:
(a) C1-8 alkyl, Ci-8 alkenyl, C1-8 alkynyl,
(b) aryl, C3-8 cycloalkyl, C3-8 cycloalkenyl,
(c) an analog of a radical of group (b) containing one or more heteroatoms selected from N, S and O.
(d) a substituted analog of a radical selected from the group consisting of groups (a), (b), and (c), said substituted analog containing one or more substituents selected from the group consisting of: hydroxyl, halogen, Ci-6 alkyl, C3-8 cycloalkyl, C3-8 heterocycloalkyl, alkyloxy, amino, alkylamino, carboxyl, nitro, sulfonylamide, alkylsulfonyl, amide, dioxoisoindole, trihaloalkyl, aryl ,heteroaryl, substituted aryl, and substituted heteroaryl, wherein said substituted aryl and substituted heteroaryl contain one or more substituents selected from the group consisting of:
Ci-6 alkyl, C3-8 cycloalkyl, C3-8 heterocycloalkyl, alkyloxy, amino, alkylamino, carboxyl, nitro, sulfonylamide, alkylsulfonyl, amide, dioxoisoindole, trihaloalkyl, and aryl; W is selected from the group consisting of C-R6 and N; Z is selected from the group consisting of C-R5 and N;
R5 and R6 are each independently selected from the group consisting of H, halogen, C1-5 alkyl, and substituted Ci-5 alkyl containing one or more substituents selected from the group consisting of methyl, ethyl, hydroxyl, hydroxylmethyl and hydroxylethyl; and
X is selected from C, N5 O and S.
2. The compound of claim 1 wherein the alkyl, alkenyl, and alkynyl groups Of R1, R2, R4, R5 and R6 are linear.
3. The compound of claim 1 wherein the alkyl, alkenyl, and alkynyl groups of Ri, R2, R4, R5 and R6 are branched.
4. The compound of claim 1, which is selected from the group consisting of: 4-benzyloxy- 1 -(2-chloro-benzyl)- 1 H-pyridin-2-one;
4-benzyloxy- 1 -(4-chloro-benzyl)- 1 H-pyridin-2-one; 4-benzyloxy- 1 -(4-nitro-benzyl)- 1 H-pyridin-2-one;
4-benzyloxy- 1 -(2,5-dichloro-benzyl)- 1 H-pyridin-2-one;
4-benzyloxy- 1 -(2,4-dichloro-benzyl)- 1 H-pyridin-2-one;
4-benzyloxy-2-(4-methoxy-benzyloxy)-pyridine; 4-benzyloxy- 1 -(4-methoxy-benzyl)- 1 H-pyridin-2-one;
4-benzyloxy-2-(4-methyl-benzyloxy)-pyridine;
4-benzyloxy-l-(4-methyl-benzyl)-lH-pyridin-2-one;
4-benzyloxy- 1 -(6-chloro-pyridin-3 -ylmethyl)- 1 H-pyridin-2-one;
4-benzyloxy-l-(3-chloro-benzyl)-lH-pyridin-2-one; 1 -benzyl-4-benzyloxy- 1 H-pyridin-2-one ;
1 -(4-amino-benzyl)-4-benzyloxy- lH-pyridin-2-one;
1 -(2,4-dichloro-benzyl)-4-hydroxy- 1 H-pyridin-2-one;
3-benzyl- 1 -(2,4-dichloro-benzyl)-4-hydroxy- 1 H-pyridin-2-one;
4-(biphenyl-4-ylmethoxy)- 1 -(2,4-dichloro-benzyl)- 1 H-pyridin-2-one; l-(2,4-dichloro-benzyl)-4-(2,4-dichloro-benzyloxy)-lH-pyridin-2-one;
4-(2-chloro-benzyloxy)-l-(2,4-dichloro-benzyl)-lH-pyridin-2-one; l-(2,4-dichloro-benzyl)-4-methoxy-lH-pyridin-2-one;
1 -(2,4-dichloro-benzyl)-4-isopropoxy- 1 H-pyridin-2-one;
4-cyclohexylmethoxy- 1 -(2,4-dichloro-benzyl)- 1 H-pyridin-2-one; 1 -(2,4-dichloro-benzyl)-4-propoxy- 1 H-pyridin-2-one;
1 -(2,4-dichloro-benzyl)-4-isobutoxy- 1 H-pyridin-2-one;
4-butoxy- 1 -(2,4-dichloro-benzyl)- 1 H-pyridin-2-one;
1 -(2,4-dichloro-benzyl)-4-octyloxy- 1 H-pyridin-2-one;
1 -(2,4-dichloro-benzyl)-4-(4-m ethyl -pentoxy)- 1 H-pyridin-2-one; 4-(but-3 -enyloxy)- 1 -(2,4-dichloro-benzyl)- 1 H-pyridin-2-one; 1 -(2,4-dichloro-benzyl)-4-pentyloxy- 1 H-pyridin-2-one; [ 1 -(2,4-dichloro-benzyl)-2-oxo- 1 ,2-dihydro-pyridin-4-yloxy] -acetic acid ethylester;
l-(2,4-dichloro-benzyl)-4-(3-methyl-butoxy)-lH-pyridin-2-one;
1 -benzyl-4-pentyloxy- 1 H-pyridin-2-one;
1 -(2-chloro-benzyl)-4-pentyloxy- 1 H-pyridin-2-one;
4-pentyloxy- 1 -propyl- 1 H-pyridin-2-one;
1 -butyl-4-pentyloxy- 1 H-pyridin-2-one; 1 -isobutyl-4-pentyloxy- 1 H-pyridin-2-one;
1 -(3 -methyl-butyl)-4-pentyloxy- 1 H-pyridin-2-one ; l-(2,4-dichloro-benzyl)-4-hexyloxy-lH-pyridin-2-one; l-(2,4-dichloro-benzyl)-4-heptyloxy-lH-pyridin-2-one;
1 -(4-chloro-benzyl)-4-penty loxy- 1 H-pyridin-2-one ; 4-aryloxy- 1 -(2,4-dichloro-benzyl)- 1 H-pyridin-2-one;
1 -(2,4-dichloro-benzyl)-4-(3-methoxy-propoxy)- 1 H-pyridin-2-one; l-(2,4-dichloro-benzyl)-4-(3-ethylammo-propoxy)-lH-pyridin-2-one;
1 -(2,4-dichloro-benzyl)-4-(2-ethoxy-ethoxy)- 1 H-pyridin-2-one;
1 -(3-methyl-but-2-enyl)-4-pentyloxy- 1 H-pyridin-2-one; 4-pentyloxy- 1 -thiazol-4-ylmethyl- 1 H-pyridin-2-one;
4-pentyloxy- 1 -pyridin-3-ylmethyl- 1 H-pyridin-2-one; l-(2,4-dichloro-benzyl)-4-(4-methyl-pent-3-enyloxy)-lH-pyridin-2-one; l-(2,4-dichloro-benzyl)-4-(3-methoxy-propoxy)-lH-pyridin-2-one;
1 -(2,4-dichloro-benzyl)-4-phenetyloxy- 1 H-pyridin-2-one; 1 -(2-methyl-benzyl)-4-pentyloxy- 1 H-pyridin-2-one;
4-pentyl-l-phenetyl-lH-pyridin~2-one; l-(2,4-dichloro-5-fluoro-benzyl)-4-pentyloxy-lH-pyridin-2-one; l-(3,4-dichloro-benzyl)-4-pentyloxy-lH-pyridin-2-one; 1 -(3,4-difluoro-benzyl)-4-pentyloxy- lH-pyridin-2-one;
4-(4-benzyloxy-butoxy)- 1 -(2,4-dichloro-benzyl) - 1 H-pyridin-2-one;
1 -(2,4-dichloro-benzyl)-4-(4-hydroxy-butoxy)- 1 H-pyridin-2-one ;
4-(5-benzyloxy-pentyloxy)- 1 -(2,4-dichloro-benzyl)- 1 H-pyridin-2-one; l-(2,4~dichloro-benzyl)-4-(5-hydroxy-pentyloxy)-lH-pyridin-2-one; 1 -(6-chloro-benzo[ 1 ,3]dioxol-5-ylmethyl)-4-pentyloxy-lH-pyridin-2-one; l-(2,4-dichloro-benzyl)-4-(2-methyl-benzyloxy)-lH-pyridin-2-one; l-(2,4-dichloro-benzyl)-4-(4-methyl-benzyloxy)-lH-pyridin-2-one;
1 -(2-nitro-benzyl)-4-pentyloxy- 1 H-pyridin-2-one ; l-(2-amino-benzyl)-4-pentyloxy-lH-pyridin-2-one; N-[2-(2-oxo-4-pentyloxy-2H-pyridin-l-ylmethyl)-phenyl]-acetamide;
4-pentyloxy- 1 -(2-trifluoromethy 1-benzyl)- 1 H-pyridin-2-one ;
N-[4-(4-benzyloxy-2-oxo-2H-pyridin-l-ylmethyl)-phenyl]acetamide; l-(2,4-dichloro-benzyl)-4-(naphthalen-2-ylmethoxy)-lH-pyridin-2-one;
1 -naphthalen-2-ylmethyl -4-pentyloxy- 1 H-pyridin-2-one; 4-benzyloxy-l-(6-chloro-benzo[l,3]dioxol-5-ylmethyl)-lH-pyridin-2-one; l-(6-chloro-benzo[l,3]dioxol-5-ylmethyl)-4-(3-methyl-butoxy)-lH-pyridin-2- one;
1 -(2-methyl-benzyl)-4-(3 -methyl-butoxy)- 1 H-pyridin-2-one;
4-(3-methyl-butoxy)-l-(2-nitro-benzyl)-lH-pyridin-2-one; 1 -(254-dichloro-benzyl)-4-pentylamino- 1 H-pyridin-2-one; l-(2,3-dichloro-benzyl)-4-pentyloxy-lH-pyridin-2-one;
1 -(2-methoxy-benzyl)-4-pentyloxy- 1 H-pyridin-2-one; l-(2,3-dimethoxy-benzyl)-4-pentyloxy-lH-pyridin-2-one; 4-(5-benzyloxy-pentyloxy)- 1 -(6-chloro-benzo[ 1 ,3] dioxol-5-ylmethyl) - 1 H- pyridin-2-one;
1 -(2-chloro-benzyl)-4-(3-methyl-butoxy)- 1 H-pyridin-2-one; l-(3,4-dichloro-benzyl)-4-(3-methyl-butoxy)-lH-pyridin-2-one; l-(2,4-dichloro-5-fluoro-benzyl)-4-(3-methyl-butoxy)-lH-pyridin-2-one; 1 -benzyl-4-(3-methyl-butoxy)-lH-pyridin~2-one; l-(4-chloro-benzyl)-4-(3-methyl-butoxy)-lH-pyridin-2-one;
1 -(2,4-dichloro-benzyl)-4-pentyloxy- lH-pyrimidin-2-one;
1 -(2,4-dichloro-benzyl)-4-(4-methyl-pentyloxy)- 1 H-pyrimidin-2-one ; l-(2,4-dichloro-benzyl)-4-phenoxy-lH-pyrimidin-2-one; 4-(butyl-methyl-amino)- 1 -(2,4-dichloro-benzyl)- 1 H-pyrimidin-2-one;
1 -(2,4-dichloro-benzyl)-4-(2-diethylamino-ethoxy)- 1 H-pyrimidin-2-one;
4-butoxy-l -(2,4-dichloro-benzyl)- 1 H-pyrimidin-2-one;
1 -(2,6-dichloro-benzyl)-4-pentyloxy- 1 H-pyridin-2-one;
1 -(2-chloro-6-fluoro-benzyl)-4-pentyloxy- 1 H-pyridin-2-one; 1 -(2-methyl-3 -nitro-benzyl)-4-pentyloxy- 1 H-pyridin-2-one;
1 -(3-amino-2-methyl-benzyl)-4-pentyloxy- 1 H-pyridin-2-one; l-(4-methoxy-3,5-dimethyl-pyridin-2-ylmethyl)-4-pentyloxy-lH-pyridin-2-one; l-(6-chloro-benzo[l,3]dioxol-5-ylmethyl)-4-(5-hydroxy-pentyloxy)-lH-pyridin- 2-one; 1 -(2-methoxy-5-nitro-benzyl)-4-pentyloxy- 1 H-pyridin-2-one;
1 -(5-amino-2-methoxy-benzyl)-4-pentyloxy- 1 H-pyridin-2-one;
1 -(2-ethyl-benzyl)-4-pentyloxy- 1 H-pyridin-2-one; l-(2-chloro-5-nitro-benzyl)-4-pentyloxy-lH-pyridin-2-one; 1 -(5-amino-2-chloro-benzyl)-4-pentyloxy- 1 H-pyridin-2-one; l-(4-methoxy-2,3-dimethyl-benzyl)-4-pentyloxy-lH-pyridin-2-one; l-(2-methyl-pyridin-3-ylmethyl)-4-pentyloxy-lH-pyridin-2-one;
N-[4-chloro-3-(2-oxo-4-pentyloxy-2H-pyridin-l-ylmethyl)-phenyl]-acetamide; l-(2,4-dichloro-benzyl)-4-(3-dimethylamino-propoxy)-lH-pyridin-2-one; 1 -(2,4-dichloro-benzyl)-4-(4-dimethylamino-butoxy)- 1 H-pyridin-2-one; l-(2,4-dichloro-benzyl)-4-(6-dimethylamino-hexyloxy)-lH-pyrimidin-2-one;
1 -(2,4-dimethyl-benzyl)-4-pentyloxy- 1 H-pyridin-2-one;
1 -(2-chloro-5-trifluoromethyl-benzyl)-4-pentyloxy- 1 H-pyridin-2-one;
1 -(2-hydroxy-benzyl)-4-pentyloxy- 1 H-pyridin-2-one; 4-(3-cyclo-propoxy)- 1 -(2,4-dichloro-benzyl)- 1 H-pyrimidin-2-one;
1 -(2,4-dichloro-benzyl)-4-(3-methyl-pentyloxy)- 1 H-pyrimidin-2-one;
1 -(2,4-dichloro-benzyl)-4-hex-4-enyloxy- 1 H-pyrimidin-2-one;
4-(2-cyclopropyl-ethoxy)- 1 -(2,4-dichloro-benzyl)- 1 H-pyrimidin-2-one; l-(2,4-dichloro-benzyl)-4-(3-methyl-pentyloxy)-lH-pyridin-2-one; l-(2,4-dichloro-benzyl)-4-(5-morpholin-4-yl-pentyloxy)-lH-pyridin-2-one; l-(2-chloro-5-methoxy-benzyl)-4-pentyloxy-lH-pyridin-2-one;
1 -(2-chloro-5-ethoxy-benzyl)-4-pentyloxy- 1 H-pyridin-2-one;
1 -(2-chloro-5-propoxy-benzyl)-4-pentyloxy- 1 H-pyridin-2-one; l-[2-chloro-5-(2-hydroxy-ethoxy)-benzyl]-4-pentyloxy-lH-pyridin-2-one; [4-chloro-3-(2-oxo-4-pentyloxy-2H-pyridin-l-ylmethyl)-oxy]-acetonitrile;
1 -[5-(2-amino-ethoxy)-2-chloro-benzyl]-4-pentyloxy- 1 H-pyridin-2-one;
N-[2-methyl-3-(2-oxo-4-pentyloxy-2H-pyridin-l-ylmethyl)-phenyl]-acetamide; l-(2-methyl-3-methylamino-benzyl)-4-phenyloxy-lH-pyridin-2-one; 1 -(3-dimethylamino-2-methyl-benzyl)-4-phenyloxy- 1 H-pyridin-2-one; l-(3-ethylamino-2-methyl-benzyl)-4-pentyloxy-lH-pyridin-2-one; l-(3-diethylamino-2-methyl-benzyl)-4-pentyloxy-lH-pyridin-2-one; l-(2-methyl-3-propylamino-benzyl)-4-pentyloxy-lH-ρyridin-2-one; l-(3-dipropylamino-2-methyl-benzyl)-4-pentyloxy-lH-pyridin-2-one; l-[3-(2-hydroxy-ethylamino)-2-methyl-benzyl]-4-pentyloxy-lH-pyridin-2-one; l-(2-chloro-5-methoxy-4-nitro-benzyl)-4-pentyloxy-lH-pyridin-2-one;
1 -(4-amino-2-chloro-5 -methoxy-benzyl)-4-pentyloxy- 1 H-pyridin-2-one;
N-[5-chloro-2-methoxy-4-(2-oxo-4-pentyloxy-2H-pyridin-l-ylmethyl)-phenyl]- acetamide; 1 -(2-chloro-5-methoxy-4-methylamino-benzyl)-4-pentyloxy- 1 H-pyridin-2-one;
1 -(2-chloro-4-dimethylamino-5-methoxy-benzyl)-4-pentyloxy- 1 H-pyridin-2- one;
1 -(2-chloro-4-ethylamino-5-methoxy-benzyl)-4-pentyloxy- 1 H-pyridin-2-one;
1 -(2-chloro-5-methoxy-4-propylamino-benzyl)-4-pentyloxy- 1 H-pyridin-2-one; 1 -[2-chloro-4-(2-hydroxy-ethylamino)-5-methoxy-benzyl]-4-pentyloxy- 1 H- pyridin-2-one;
1 -(4-amino-6-chloro~3 -methoxy-2-nitro-benzyl)-4-pentyloxy- 1 H-pyridin-2-one;
1 -(2,4-diamino-6-chloro-3-methoxy-benzyl)-4-pentyloxy- 1 H-pyridin-2-one; l-(2,5-dichloro-6-methoxy-pyrimidin-4-ylmethyl)-4-pentyloxy-lH-pyridin-2- one;
1 -(254-dichloro-benzenesulfonyl)-4-pentyloxy- 1 H-pyridin-2-one;
1 -(4-methanesulfonyl-benzyl)-4-pentyϊoxy- 1 H-pyridin-2-one; l-(4-amino-2-chloro-5-hydroxy-benzyl)-4-pentyloxy-lH-pyridin-2-one; 4-(4-bromo-butoxy)-l-(2,4-dichloro-benzyl)-lH-pyridin-2-one;
4-[l-(2,4-dichloro-benzyl)-2-oxo-l,2-dihydro-pyridin-4-yloxy]- butylammonium; l-(5-chloro-2,6-dimethoxy-pyrimidin-4-ylmethyl)~4-pentyloxy-lH-pyridin-2- one; l-(2-aniino-5-chloro-6-methoxy-pyrimidin-4-ylmethyl)-4-pentyloxy-lH- pyridin-2-one;
1 -(6-amino-2, 5 -dichloro-pyrimidin-4-y lmethyl)-4-pentyloxy- 1 H-pyridin-2-one ;
5-chloro-6-(2-oxo-4-pentyloxy-2H-pyridin-l-ylmethyl)-3H-benzoxazole-2-one;
1 -(2-chloro-4-hydroxy-benzyl)-4-pentyloxy- 1 H-pyridin-2-one; 1 -(2-chloro-4-isopropoxy-benzyl)-4-pentyloxy- 1 H-pyridin-2-one;
2-[3-(2-oxo-4-pentyloxy-2H-pyridin-l-yl)-propyl]-isoindole-l,3-dione; l-(3-amino-propyl)-4-pentyloxy-lH-pyridin-2-one;
N-[3-(2-oxo-4-pentyloxy-2H-pyridin- 1 -yl)-propyl]-acetamide;
1 -(3 -dimethylamino-propyl)-4-pentyloxy- 1 H-pyridin-2-one; 1 -(2,4-dichloro-benzyl)-6-methyl-4-pentyloxy- 1 H-pyridin-2-one;
1 -(2,4-dichloro-benzyl)-6-methyl-3 -pentyl-4-pentyloxy- 1 H-pyridin-2-one;
1 -(2-amino-ethyl)-4-pentyloxy- 1 H-pyridin-2-one;
N-[2-(2-oxo-4-pentyloxy-2H-pyridin-l-yl)-ethyl]-acetamide;
N-[I5I -dimethyl-2-(2-oxo-4-pentyloxy-2H-pyridin- 1 -yl)-ethyl] - methanesulfonamide;
N- [ 1 -(2-oxo-4-pentyloxy-2H-pyridin- 1 -ylmethyl)-propyl] -methanesulfonamide; l-(7-nitro-benzo[l,3]dioxol-5-ylmethyl)-4-pentyloxy-lH-pyridin-2-one;
1 -(2-chloro-3-nitro-benzyl)-4-pentyloxy- 1 H-pyridin-2-one; 1 -(3-amino-2-chloro-benzyl)-4-pentyloxy-lH-pyridin-2-one;
N-[2-chloro-3-(2-oxo-4-pentyloxy-2H-pyridin-l-ylmethyl)-phenyl]-acetamide;
N-[2-chloro-3-(2-oxo-4-pentyloxy~2H-pyridin-l-ylmethyl)-phenyl]- methanesulfonamide;
N5N' -[2-chloro-3 -(2-oxo-4-pentyloxy-2H-pyridin- 1 -ylmethyl)-phenyl] - dimethanesulfonamide;
1 - [2-chloro-3 -(2-hydroxy-ethylamino)-benzyl] -4-pentyloxy- 1 H-pyridin-2-one ;
4-chloro-2-(2-chloro-benzyl)-5-pentyloxy-2H-pyridazin-3-one;
2-(2-chloro-benzyl)-5-pentyloxy-2H-pyridazin-3-one; l-(3-amino-2,6-dichloro-benzyl)-4-pentyloxy-lH-pyridin-2-one; l-(3-benzyloxy-2-chloro-4-methoxy-benzyl)-4-pentyloxy-lH-pyridin-2-one; l-(2-chloro-3,4-dimethoxy-benzyl)-4-pentyloxy-lH-pyridin-2-one;
1 -(2-chloro-3 -hydroxy-4-methoxy-benzyl)-4-pentyloxy- 1 H-pyridin-2-one; l-[2-chloro-4-rnethoxy-3-(2-methoxy-ethoxy)-benzyl]-4-pentyloxy-lH-pyridin- 2-one; 1 -[2-chloro-4-methoxy-3-(2-pyrrolidin- 1 -yl-ethoxy)-benzyl]-4-pentyloxy- 1 H- pyridin-2-one; l-[2-chloro-3-(2-dimethylamino-ethoxy)-4-methoxy-benzyl]-4-pentyloxy-lH- pyridin-2-one;
2-{3-[2-chloro-6-methoxy-3-(2-oxo-4-pentyloxy-2H-pyridin-l-ylmethyl)- phenoxylj-propyl} -isoindole- 1 ,3-dione;
l-[3-(2-dimethylamino-ethoxy)-2-methyl-benzyl]-4-pentyloxy-lH-pyridin-2- one;
l-[2-chloro-3-(2-dimethylamino-ethylamino)-benzyl]-4-pentyloxy-lH-pyridin- 2-one;
l-[2,6-dichloro-3-(2-hydroxy-ethylamino)-benzyl]-4-ρentyloxy-lH-pyridin-2- one;
1 - [2, 6-dichloro-3 -(2-dimethylamino-ethylamino)-benzyl] -4-pentyloxy- 1 H- pyridin-2-one; l-[2,6-dichloro-3-(3-hydroxy-propylamino)-benzyl]-4-pentyloxy-lH-pyridin-2- one; l-[2,6-dichloro-3-(3dimethylamino-propylamino)-benzyl]-4-pentyloxy-lH- pyridin-2-one; l-[3-(3-amino-propylamino)-2,6-dichloro-benzyl]-4-pentyloxy-lH-pyridin-2- one;
1 -(3-fluoro-2-methyl-benzyl)-4-pentyloxy- 1 H-pyridin-2-one; l-(2-chloro-3-dimethylaminomethyl-4-fluoro-benzyl)-4-pentyloxy-lH-pyridin- 2-one;
1 -(2,6-dichloro-3-methylamino-benzyl)-4-pentyloxy- 1 H-pyridin-2-one; l-(2,6-dichloro-3-dimethylamino-benzyl)-4-pentyloxy-lH-pyridin-2-one;
[2-chloro-3 -(2-oxo-4-pentyloxy-2H-pyridin- 1 -ylmethyl)-phenylamino] -acetic acid; l-(6-chloro-benzo[l53]dioxol-5-ylmethyl)-4-(pyridin-4-ylmethoxy) -lH-pyridin- 2-one; l-(6-chloro-benzo[l,3]dioxol-5-ylmethyl)-4-(6-chloro-pyridin-3-ylmethoxy)- lH-pyridin-2-one;
l-(6-chloro-benzo[l,3]dioxol-5-ylmethyl)-4-(4-methoxy-3,5-dimethylpyridin-2- ylmethoxy) -lH-pyridin-2-one; l-(6-chloro-benzo[l,3]dioxol-5-ylmethyl)-4-(2-methyl-pyridin-3-ylmethoxy)-
1 H-pyridin-2-one; l-(6-chloro-benzo[l,3]dioxol-5-ylmethyl)-4-(thiazol-4-ylmethoxy) -lH-pyridin- 2-one; l-(6-chloro-benzo[l,3]dioxol-5-ylmethyl)-4-(pyridin-2-ylmethoxy)-lH-pyridin- 2-one; pentanoic acid 1 -(6-chloro-benzo[l ,3]dioxol-5-ylmethyl)-2-oxo-l ,2-dihydro- pyridin-4-yl ester; hexanoic acid l-(6-chloro-benzo[l,3]dioxol-5-ylmethyl)-2-oxo-l,2-dihydro- pyridin-4-yl ester; l-(2-chloro-3-trifluoromethyl-benzyl)-4-pentyloxy-lH-pyridin-2-one; thiophene-2-carboxyl acid 1 -(6-chloro-benzo[ 1 ,3]dioxol-5-ylmethyl)-2-oxo- 1 ,2- dihydro-pyridin-4-yl ester; toluene-4-sulfonic acid 1 -(6-chloro-benzo[l ,3]dioxol-5-ylmethyl)~2-oxo-l ,2- dihydro-pyridin-4-yl ester; 1 -(6-chloro-benzo[l ,3]dioxol-5-ylmethyl)-4-(4,4,5,5,5-pentafluoro-pentyloxy)-
1 H-pyridin-2-one ; l-(6-chloro-benzo[l,3]dioxol-5-ylmethyl)-4-(2-dimethylamino-ethoxy)-lH- pyridin-2-one;
1 -(2,4-dichloro-benzyl)-4-(5 -fluoro-pentyloxy)- 1 H-pyridin-2-one; 3-[l-(2,4-dichloro-benzyl)-2-oxo-l,2-dihydro-pyridin-4-yloxymethyl]-indole-l- carboxyl acid tetra-butyl ester;
1 -(2,4-dichloro-benzyl)-4-(2-thiophen-2-yl-ethoxy)- 1 H-pyridin-2-one; 1 -(2,4-dichloro-benzyl)-4-(2-thiophen-3 -yl-ethoxy)- 1 H-pyridin-2-one; 1 -(2,4-dichloro-benzyl)-4-(2-pyrrol- 1 -yl-ethoxy)- 1 H-pyridin-2-one; l~(2,4-dichloro-benzyl)-4~(3~pyrrol-l-yl-propoxy)-lH-pyridin-2-one; l-(3-amino-2-methyl-benzyl)-4-(2-thiophen-2-yl-ethoxy)-lH-pyridin-2-one; l-(3-amino-2-methyl-benzyl)-4-(2-pyrrol-l-yl-ethoxy)-lH-pyridin-2-one; l-(3-amino-2-methyl-benzyl)-4-[2-(4-methyl-thiazol-5-yl)-ethoxy]-lH-pyridin- 2-one; l-(3-amino-2-methyl-benzyl)-4-(2-(5-bromothiophen-2-yl)-ethoxy)-lH-pyridin- 2-one; l-(3-amino-2-methyl-benzyl)-4-(2-(5-fluorothiophen-2-yl)-ethoxy)-lH-pyridin- 2-one; l-[3-(2-hydroxy-ethylamino)-2-methyl-benzyl]-4-(2-thiophen-2-yl-ethoxy)-lH- pyridin-2-one;
2- {2-methyl-3-[2-oxo-4-(2-thiophene-2-yl-ethoxy)-2H-pyridin- 1 -ylmethyl]- phenylamino } -acetamide ; l-[3-(cyclopropylmethyl-amino)-2-methyl-benzyl]-4-(2-thiophen-2-yl-ethoxy)- 1 H-pyridin-2-one ;
N-{2-methyl-3-[2-oxo-4-(2-thiophen-2-yl-ethoxy)-2H-pyridin-l-ylmethyl]- phenylamino } -acetonitrile;
N-(2-{2-methyl-3-[2-oxo-4-(2-thiophen-2-yl-ethoxy)-2H-pyridin-l-ylmethyl]- phenylamino } -ethyl)-acetamide; 1 - [2-methyl-3-(2-pyrrol- 1 ~yl~ethylamino)-benzyl] -4-(2-thiophen-2-yl-ethoxy)- lH-pyridin-2-one;
l-[2-methyl-3-(2-oxo-2-pyrrolidin-l-yl-ethylamino)-benzyl]-4-(2-thiophen-2-yl- ethoxy)- 1 H-pyridin-2-one; 1 -[2-methyl-3-(2-oxo-2-piperidin-l -yl-ethylamino)-benzyl]-4-(2-thiophen~2-yl- ethoxy)- 1 H-pyridin-2-one;
N,N-dimethyl-2-{2-methyl-3-[2-oxo-4-(2-thiophen-2-yl-ethoxy)-2H-pyridin-l- ylmethyl]-phenylamino}-acetamide; l-{2-methyl-3-[2-(4-methyl-piperazin-l-yl)-2-oxo-ethylamino]-benzyl}-4-(2- thiophen-2-yl-ethoxy)- 1 H-pyridin-2-one; l-[2-methyl-3-(2-morpholin-4-yl-2-oxo-ethylamino)-benzyl]-4-(2-thioprien-2-yl- ethoxy)~lH-pyridin-2~one; l-(3-amino-2-methyl-benzyl)-4-(2-furan-2-yl-ethoxy)-lH-pyridin-2-one; l-(3-amino-2-methyl-benzyl)-4-[2-(5-methyl-thiophen-2-yl)-ethoxy]-lH-pyridin- 2-one;
1 -(3 -amino-2-methyl-benzyl)-4- [2-(5 -chloro-thiophen-2-yl)-ethoxy] - 1 H-pyridin- 2-one; l-(2,4-dichloro-benzyl)-4-[2-(3-methyl-thiophen-2-yl)-ethoxy]-lH-pyridin-2- one; l-(3-amino-2-methyl-benzyl)-4-(2-benzo[b]thiophen-3-yl-ethoxy)-lH-pyridin-2- one; l-(3-amino-2-methyl-benzyl)-4-[2-(5-chloro-3-methyl-benzo[b]thiophen-2-yl)- ethoxy]-lH-pyridin-2-one; l-(3-amino-2-methyl-benzyl)-4-[2-(3-methyl-benzo[b]thiophen-2-yl)-ethoxy]- lH-pyridin-2-one;
l-(3-amino-2-methyl-benzyl)-4-[2-(5-methyl-ftιran-2-yl)-ethoxy]-lH-pyridin-2- one;
l-(3-amino-2-methyl-benzyl)-4-[2-(5-ethyl-furan-2-yl)-ethoxy]-lH-pyridin-2- one;
5-[l-(3-amino-2-methyl-benzyl)-2-oxo-l,2-dihydro-pyridin-4-yloxymethyl]- furan-2-carboxylic acid ethyl ester; l-[3-(2-dimethylamino-ethylamino)-2-methyl-benzyl]-4-(2-thiophen-2-yl- ethoxy)- 1 H-pyridin-2-one; l-(3-amino-2-methyl-benzyl)-4-[2-(5-niethylsulfanyl-thiophen-2-yl)-ethoxy]-lH- pyridin-2-one;
1 -(3-amino-2-methyl-benzyl)-4-(2-benzofuran-2-yl-ethoxy)- 1 H-pyridin-2-one; l-(3-amino-2-methyl-benzyl)-4-[2-(3-methyl-isoxazol-5-yl)-ethoxy]-lH-pyridin- 2-one; l-(3-amino-2-methyl-benzyl)-4-[2-(4,5-dimethyl-thiophen-2-yl)-ethoxy]-lH- pyridin-2-one; l-(3-amino-2-methyl-benzyl)-4-[2-(5-ethyl-thiophen-2-yl)-ethoxy]-lH-pyridin-2- one;
1 -(3-amino-2,6-dichloro-benzyl)-4-(2-thiophen-2-yl-ethoxy)- 1 H-pyridin-2-one; N- {2-methyl-3 - [2-oxo-4-(2-thiophen-2-yl-ethoxy)-2H-pyridin- 1 -ylmethyl] - phenyl } -acetamide ;
1 - [2-methyl-3 -(2-piperidin- 1 -yl-ethylamino)-benzyl] -4-(2-thiophen-2-yl-ethoxy)- 1 H-pyridin-2-one; l-[2-methyl-3-(2-morpholin-4-yl-ethylamino)-benzyl]-4-(2-thiophen-2-yl- ethoxy)- 1 H-pyridin-2-one;
N-{2-methyl-3-[2-oxo-4-(2-thiophen-2-yl-ethoxy)-2H-pyridin-l-ylmethyl]- phenyl } -methanesulfonamide;
l-(3-amino-2-methyl-benzyl)-4-[2-(4-bromo-thiophen-2-yl)-ethoxy]-lH-pyridin- 2-one;
l-(6-chloro-benzo[l,3]dioxol-5-ylmethyl)-4-(2-pyrrol-l-yl-ethoxy)-lH-pyridin- 2-one; l-(6-chloro-benzo[l,3]dioxol-5-ylmethyl)-4-(2-thiophen-2-yl-ethoxy)-lH- pyridin-2-one; 1 -[2-methyl-3-(2-pyrrolidin-l -yl-ethylamino)-benzyl]-4-(2-tbiophen-2-yI- ethoxy)- 1 H-pyridin-2-one ;
N-(2-{2-methyl-3-[2-oxo-4-(2-thiophen-2-yl-ethoxy)-2H-pyridin-l-ylmethyl]- phenylamino } -ethyl)-acetamide ;
1 - {2-methyl-3 -[(pyridin-3 -ylmethyl)-amino]-benzyl } -4-(2-thiophen-2-yl- ethoxy)-lH-pyridin-2-one;
2-methyl-3-[2-oxo-4-(2-thiophen-2-yl-ethoxy)-2H-pyridin-l-ylmethyl]-phenyl ester; l-{2-methyl-3-[(pyridin-4-ylmethyl)-amino]-benzyl}-4-(2-thiophen-2-yl- ethoxy)- 1 H-pyridin-2-one; l-{2-methyl-3-[(thiazol-4-ylmethyl)-amino]-benzyl}-4-(2-thiophen-2-yl-ethoxy)-
1 H-pyridin-2-one; l-[3-(4-methoxy-benzyloxy)-2-methyl-benzyl]-4-(2-thiophen-2-yl-ethoxy)-lH- pyridin-2-one; l-{3-[(3.5-dimethyl-isoxazol-4-ylmethyl)-amino]-2-methyl-benzyl}-4-(2- thiophen-2-yl-ethoxy)- 1 H-pyridin-2-one;
l-(3-hydroxy-2-methyl-benzyl)-4-(2-thiophen-2-yl-ethoxy)-lH-ρyridin-2-one; l-{2-methyl-3-[(l-methyl-pyrrolidin-2-ylmethyl)-amino]-benzyl}-4-(2-thiophen- 2-yl-ethoxy)- 1 H-pyridin-2-one;
l-{2-methyl-3-[2-(l-methyl-ρyrrolidin-2-yl)-ethylamino]-benzyl}-4-(2-thiophen-
2-yl-ethoxy)- 1 H-pyridin-2-one;
(2-{2-methyl-3-[2-oxo-4-(2-thiophen-2-yl-ethoxy)-2H-pyridin-l-ylmethyl]- phenylamino}-ethyl)-phosphonic acid diethyl ester;
4-(isobuthylthio)-l-(2-methyl-3-nitrobenzyl)pyridine-2(lH)-one; l-(3-amino-2-methylbenzyl)-4-(isobutylthio)pyridine-2(lH)-one;
" l-(3-amino-2-methylbenzyl)-4-(furan-2-ylmethylthio)pyridine-2(lH)-one; 1 -(3-amino-2-methylbenzyl)-4-(pentylthio)pyridine-2-(l H)-one; l-(3-amino-2-methylbenzyl)-4-(phenethylthio)pyridine-2(lH)-one; 1 -(3 -amino-2-methylbenzyl)-4-(butylthio)pyridine-2( 1 //)-one ; 1 -(3 -amino-2-methylbenzyl)-4-(thiophen-2-ylmethylthio)pyridine-2( 1 H)-one; l-(3-amino-2-methylbenzyl)-4-(pentylthio)pyridine-2(lH)-one; l-(3-amino-2-methylbenzyl)-4-(propylthio)pyridine-2(lH)-one; l-(3-amino-2-methylbenzyl)-4-(l-methylbutylthio)pyridine-2(lH)-one; N,N-dimethyl-3-(2-methyl-3-((2-oxo-4-(2-(thioρhen-2-yl)ethoxy)pyridin-l(2H)- yl)methyl)phenylamino)propane- 1 -sulfonamide; l-(3-amino-2-methylbenzyl)-4-(2-(thiophene-2-yl)ethylamino)pyridine-2-(lH)- one.
5. A method of preparing the compound of claim 1 comprising: forming a solution of a pyridone or pyridazine derivative comprising an alcohol or amine functionality and NaH or potassium t-butoxide in DMF; combining said solution with a halide compound of the formula k-m-h where h is chloride or bromide; m is benzyl, benzyloxy, or ylmethyl; and k is 2-chloro, 3-chloro, 4-chloro, 4-nitro, 2,5-dichloro, 2,4-dichloro, 4-menthoxy, 4-methyl, or 6-chloro-pyridin- 3-, or 4-amino; stirring said combination for 30 minutes at room temperature to form a reaction product which includes one or more of the compounds described in claim 1.
6. The method of claim 5 and further comprising: isolating said one or more compounds described in claim 1 from said reaction product by column chromatography.
7. A method of claim 6 and further comprising: hydrogenating said isolated product with Pd/C to form a compound having a hydroxyl substituent.
8. A method of claim 7 and further comprising: substituting said hydroxyl substitutent by a radical selected from the group consisting of (a) H; (b) C1-8 alkyl, Ci-8 alkenyl, C1-8 alkynyl; (c) aryl, C3-8 cycloalkyl or C3- 8 cycloalkenyl; (d) an analog of the radicals of group b containing one or more heteroatoms selected from N, S or O; and (e) a substituted analog of a member of groups (b), (c), and (d), said substituted analog containing one or more substituents selected from the group consisting of hydroxyl, halogen, Ci-6alkyl, C3-8 cycloalkyl, C3-8 heterocycloalkyl, alkyloxy, amino, alkylamino, carboxyl, nitro, sulfonylamide, alkylsulfonyl, amide, dioxoisoindole, trihaloalkyl, aryl and heteroaryl.
9. An anti-bacterial composition comprising the compound of claim 1 as an active ingredient.
10. The anti-bacterial composition of claim 9, which is in the form of a formulation comprising the compound of claim 1 in the range of 50 to 5,000 mg, the formulation being selected from the group consisting of oral, sublingual, inhalation, topical, rectal, and injection formulations.
11. The anti-bacterial composition of claim 10, which is in the form of a formulation comprising the compound of claim 1 in the range of 150 to 3,000 mg.
12. The anti-bacterial composition of claim 10, which is in the form of a formulation comprising the compound of claim 1 in the range of 50 to 2,000 mg.
13. A method for inhibiting the activity of Fab I, wherein the method comprises administering to a human in need thereof, an effective amount of a compound of claim 1.
14. A method for treating bacteria-related disease, wherein the method comprises administering to a human in need thereof, an effective amount of a formulation of claim 10.
15. The method of claim 14, wherein said formulation is in the form of a tablet, capsule or pill.
16. The method of claim 14, wherein the administration is by subcutaneous, intravenous, intramuscular, intra-articular, intra-synovial, intrasternal, intrathecal, intrahepatic, intralesional and intracranial injection.
17. A kit for use in the treatment of bacteria-related disease which comprises: (a) the formulation of claim 10 and (b) a syringe.
18. A kit for use in a method of treating bacteria-related disease comprising the formulation of claim 10 in the form of a powder, granules, or concentrate and a solvent for reconstituting said pharmaceutical composition to provide an oral dosage form.
19. A compound of claim 1 wherein X is O.
20. A compound of claim 19 wherein,
A is CH; B is CH2;
Z is CH; and W is CH.
21. A compound of claim 19 wherein, A is CH; B is CH2; Z is CH; and W is N.
22. A compound of claim 19 wherein:
A is CH; B is CH2; W is CH; and Z is N.
23. A compound of claim 20 wherein,
R4 is selected from the group consisting of: aryl and a substituted aryl containing one or more substituents selected from the group consisting of hydroxyl, halogen, C1-6alkyl, C3-8 cycloalkyl, C3-8 heterocycloalkyl, alkyloxy, amino, alkylamino, carboxyl, nitro, sulfonylamide, alkylsulfonyl, amide, dioxoisoindole, trihaloalkyl, and aryl.
24. The compound of claim 23, wherein R1 is selected from the group of radicals consisting of:
(a) H,
(b) C]-S alkyl, Cj-s alkenyl, Ci-8 alkynyl, and
(c) a substituted analog of a radical of group (b), said substituted analog containing one or more substituents selected from the group consisting of hydroxyl, halogen, Cj-6 alkyl, C3-8 cycloalkyl, C3-8 heterocycloalkyl, alkyloxy, amino, alkylamino, carboxyl, nitro, sulfonylamide, alkylsulfonyl, amide, dioxoisoindole, trihaloalkyl, aryl, and heteroaryl.
25. A compound of claim 1 wherein : B is NH; and R4 is selected from the group consisting of:
(a) Ci-8 alkyl, Cj-8 alkenyl, Ci-8 alkynyl, aryl, and a heteroaryl containing one or more heteroatoms selected from N, S and O, and (b) a substituted radical of group (a) containing one or more substituents selected from the group consisting of hydroxyl, halogen, C1-6 alkyl, C3-8 cycloalkyl, C3-8 heterocycloalkyl, alkyloxy, amino, alkylamino, carboxyl, nitro, sulfonylamide, alkylsulfonyl, amide, dioxoisoindole, trihaloalkyl, and aryl.
26. A compound of claim 1 wherein:
X is S.
A is CH;
B is CH2;
Z is CH; and W is CH.
27. A compound of claim 1 which is an acid selected from the group consisting of hydrochloric, sulfuric, phosphoric, p-toluenesulfonic, methanesulfonic, hydrobromic and camphorsulfonic .
PCT/KR2006/004133 2005-10-13 2006-10-13 Fab i inhibitor and process for preparing same Ceased WO2007043835A1 (en)

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US20070135465A1 (en) 2007-06-14
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CA2625962C (en) 2014-11-04
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US7973060B2 (en) 2011-07-05
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