WO2000039082A2 - 1,2-annelated quinoline derivatives - Google Patents
1,2-annelated quinoline derivatives Download PDFInfo
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- WO2000039082A2 WO2000039082A2 PCT/EP1999/010214 EP9910214W WO0039082A2 WO 2000039082 A2 WO2000039082 A2 WO 2000039082A2 EP 9910214 W EP9910214 W EP 9910214W WO 0039082 A2 WO0039082 A2 WO 0039082A2
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- 0 C*1ccc(C(*)(*)c(cc2)cc(*(*3)c4ccccc4)c2N=C3I)cc1 Chemical compound C*1ccc(C(*)(*)c(cc2)cc(*(*3)c4ccccc4)c2N=C3I)cc1 0.000 description 3
- QKWWDTYDYOFRJL-UHFFFAOYSA-N COC(CN)OC Chemical compound COC(CN)OC QKWWDTYDYOFRJL-UHFFFAOYSA-N 0.000 description 1
- IVIRNJUGXAMETB-UHFFFAOYSA-N Cc1nc(ccc(C(c2cnc[n]2C)(c(cc2)ccc2Cl)O)c2)c2c(-c2cccc(Cl)c2)c1 Chemical compound Cc1nc(ccc(C(c2cnc[n]2C)(c(cc2)ccc2Cl)O)c2)c2c(-c2cccc(Cl)c2)c1 IVIRNJUGXAMETB-UHFFFAOYSA-N 0.000 description 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—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
- C07D401/02—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
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- 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
- A61K31/47—Quinolines; Isoquinolines
- A61K31/4738—Quinolines; Isoquinolines ortho- or peri-condensed with heterocyclic ring systems
- A61K31/4745—Quinolines; Isoquinolines ortho- or peri-condensed with heterocyclic ring systems condensed with ring systems having nitrogen as a ring hetero atom, e.g. phenantrolines
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- 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
- A61K31/495—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
- A61K31/498—Pyrazines or piperazines ortho- and peri-condensed with carbocyclic ring systems, e.g. quinoxaline, phenazine
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- 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
- A61K31/495—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
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/519—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/06—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
Definitions
- the present invention is concerned with novel 1,2-annelated quinoline derivatives, the preparation thereof, pharmaceutical compositions comprising said novel compounds and the use of these compounds as a medicine as well as methods of treatment by administering said compounds.
- Oncogenes frequently encode protein components of signal transduction pathways which lead to stimulation of cell growth and mitogenesis.
- Oncogene expression in cultured cells leads to cellular transformation, characterized by the ability of cells to grow in soft agar and the growth of cells as dense foci lacking the contact inhibition exhibited by non-transformed cells. Mutation and/or overexpression of certain oncogenes is frequently associated with human cancer.
- a particular group of oncogenes is known as ras which have been identified in mammals, birds, insects, mollusks, plants, fungi and yeasts.
- the family of mammalian ras oncogenes consists of three major members ("isoforms") : H-r s, K-ras and N-ras oncogenes. These ras oncogenes code for highly related proteins genetically known as p21 ⁇ 5 . Once attached to plasma membranes, the mutant or oncogenic forms of p21 ra,y will provide a signal for the transformation and uncontrolled growth of malignant tumor cells. To acquire this transforming potential, the precursor of the p21 xs' oncoprotein must undergo an enzymatically catalyzed farnesylation of the cysteine residue located in a carboxyl-terminal tetrapeptide.
- farnesyl transferase inhibitors can be very useful as anticancer agents for tumors in which ras contributes to transformation.
- the K-ras B isoform has been observed to be the dominant isoform which is mutated in human cancers, particular in colon (50% incidence) and pancreatic (90% incidence) cancers.
- ras protein activation in the K-ras B isoform transformed cancers is resistant to inhibition of farnesyl transferase.
- the isoform confers resistance to farnesyl transferase inhibitors, but makes this isoform also substrate for geranylgeranyl transferase I. Therefore, inhibitors of geranylgeranyl transferase may inhibit the aberrant growth of K-ras transformed tumors which are resistant to farnesyl transferase inhibitors.
- the present invention concerns compounds of formula
- R 6 , R 7 and R 8 are independently hydrogen, C]- alkyl, hydroxy, C ⁇ - alkyloxy, aryloxy, C ⁇ - 4 alkyloxycarbonyl, hydroxyC ⁇ - alkyl, C ⁇ - 4 alkyloxyC ⁇ - alkyl, mono- or di(C ⁇ - 4 alkyl)aminoC ⁇ - alkyl, cyano, amino, thio, C ⁇ - alkylthio, arylthio or aryl; >Y'-Y 2 - is a trivalent radical of formula >CH-CHR 9 - (y-1),
- each R 9 independently is hydrogen, halo, halocarbonyl, aminocarbonyl, hydroxyC ⁇ - 4 alkyl, cyano, carboxyl, C ⁇ - 4 alkyloxy, C ⁇ - 4 alkyloxyC 1-4 alkyl, C ⁇ - alkyloxycarbonyl, mono- or di(C ⁇ - 4 alkyl)amino, mono- or di(C 1 - 4 alkyl)aminoC ⁇ - 4 alkyl, aryl; r and s are each independently 0, 1, 2, 3, 4 or 5; t is O, 1, 2 or 3; each R 1 and R 2 are independently hydroxy, halo, cyano, C ⁇ _6alkyl, trihalomethyl, trihalomethoxy, C 2 - 6 alkenyl, C ⁇ alkyloxy, hydroxyC ⁇ - 6 alkyloxy, C ⁇ - 6 alkylthio, C !
- R 3 is hydrogen, halo, C,- 6 alkyl, cyano, halo - ⁇ alkyl, hydroxyC 1-6 alkyl, cyanoC,- 6 alkyl, aminoC ⁇ - 6 alkyl, C,- 6 alkyloxyC,- 6 alkyl, C 1 - 6 alkylthioC 1 - 6 alkyl, aminocarbonylCj-salkyl, hydroxycarbonyl, hydroxycarbonylC ⁇ - 6 alkyl, C 1-6 alkyloxycarbonylC ⁇ - 6 alkyl, d-ealkylcarbonylC ⁇ alkyl, C ⁇ - 6 alkyloxycarbonyl, aryl, aryld- 6 alkyloxyCi-6alkyl, mono- or d -ealky aminoCi- ⁇ alkyl; or a radical of formula
- R 10 is hydrogen, C ⁇ - 6 alkyl, C ⁇ - 6 alkylcarbonyl, aryl, arylC,- 6 alkyl,
- R 11 is hydrogen, C ⁇ - 6 alkyl, aryl or arylC ⁇ alkyl
- R 12 is hydrogen, C,- 6 alkyl, aryl, hydroxy, amino, C ⁇ alkyloxy, aryld- e alkyl, C L ⁇ alkylcarbonylamino, mono- or di(C ⁇ - 6 alkyl)amino, C ⁇ - 6 alkylcarbonyl, aminocarbonyl, arylcarbonyl, haloC ⁇ - 6 alkylcarbonyl, arylC ⁇ - 6 alkylcarbonyl, C ⁇ alkyloxycarbonyl, C Ls alkyloxyC L ⁇ alkylcarbonyl, mono- or di(C 1 - 6 alkyl)aminocarbonyl wherein the alky
- Alk is C ⁇ - 6 alkanediyl
- R 13 is hydrogen, C ⁇ - 6 alkyl, C ⁇ - 6 alkylcarbonyl, hydroxyC 1 - 6 alkyl, aryl or arylC,- 6 alkyl;
- R 14 is hydrogen, C ⁇ - 6 alkyl, aryl or arylQ- e alkyl;
- R 15 is hydrogen, C]- 6 alkyl, d- 6 alkylcarbonyl, aryl or arylQ-galkyl;
- R 4 is a radical of formula
- R 16 is hydrogen, halo, aryl, C ⁇ - 6 alkyl, hydroxyC ⁇ - 6 alkyl, C ⁇ - 6 alkyloxyC ⁇ - 6 alkyl, C ⁇ _ 6 alkyloxy, C ⁇ - 6 alkylthio, amino, mono- or di(C ⁇ - 4 alkyl)amino, hydroxycarbonyl, C ⁇ - 6 alkyloxycarbonyl, C ⁇ .6alkylthioC ⁇ -6 alkyl, C,- 6 alkylS(O)C,- 6 alkyl or C,- 6 alkylS(O) 2 C,- 6 alkyl; R 16 may also be bound to one of the nitrogen atoms in the imidazole ring of formula (c-1) or (c-2), in which case the meaning of R 16 when bound to the nitrogen is limited to hydrogen, aryl, C ⁇ - 6 alkyl, hydroxyC ⁇ alkyl, C,- 6 alky
- R 5 is C 1-6 alkyl , C ⁇ - 6 alkyloxy or halo; aryl is phenyl, naphthalenyl or phenyl substituted with 1 or more substituents each independently selected from halo, C,- 6 alkyl, C,- 6 alkyloxy or trifluoromethyl .
- a special group of compounds contains those compounds of formula (I) wherein each R 1 and R 2 are independently hydroxy, halo, cyano, C ⁇ -6alkyl, trihalomethyl, trihalomethoxy, C 2 . 6 alkenyl, C ⁇ - 6 alkyloxy, hydroxyC ⁇ - 6 alkyloxy, d- 6 alkylthio, C 1 - 6 alkyloxyC ⁇ - 6 alkyloxy, d- ⁇ alkyloxycarbonyl, aminoC 1-6 alkyloxy, mono- or di(C ⁇ - 6 alkyl)amino, mono- or di(C ⁇ -6 alkyl)aminoC ⁇ - 6 alkyloxy, aryl, aryld- 6 alkyl, aryloxy or arylC,- 6 alkyloxy, hydroxycarbonyl, C,- 6 alkyloxycarbonyl; or two R 1 or R 2 substituents adjacent to one another on the phenyl ring
- R 16 is hydrogen, halo, aryl, d- 6 alkyl, hydroxyC ⁇ - 6 alkyl, C ⁇ - 6 alkyloxyd- 6 alkyl, d- 6 alkyloxy, C 1-6 alkylthio, amino, mono- or di(C ⁇ - 4 alkyl)amino, hydroxycarbonyl, C,- 5 alkyloxycarbonyl, d-6alkylthioC ⁇ - 6 alkyl, C ⁇ - 6 alkylS(O)C ⁇ - 6 alkyl or d- 6 alkylS(O) 2 d- 6 alkyl; R 16 may also be bound to one of the nitrogen atoms in the imidazole ring of formula (c-1), in which case the meaning of R 16 when bound to the nitrogen is limited to hydrogen, aryl, C 1-6 alkyl, hydroxyC 1-6 alkyl, C,- 6 alkyloxyC 1-6 alkyl, - C,- 6 al
- R 17 is hydrogen, d- 6 alkyl, trifluoromethyl or di(C ⁇ - 4 alkyl)aminosulfonyl.
- halo is generic to fluoro, chloro, bromo and iodo
- Ci ⁇ alkyl defines straight and branched chain saturated hydrocarbon radicals having from 1 to 4 carbon atoms such as, e.g.
- C ⁇ _6alkyl includes C ⁇ _ 4 alkyl and the higher homologues thereof having 5 to 6 carbon atoms such as, for example, pentyl, 2-methyl- butyl, hexyl, 2-methylpentyl and the like;
- Ci.galkanediyl defines bivalent straight and branched chained saturated hydrocarbon radicals having from 1 to 6 carbon atoms, such as, for example, methylene, 1,2-ethanediyl, 1,3-propanediyl, 1,4-butanediyl, 1,5-pentanediyl, 1,6-hexanediyl and the branched isomers thereof;
- C 2 -6 lkenyl defines straight and branched chain hydrocarbon radicals containing one double bond and having from 2 to 6 carbon atoms such as, for example, ethenyl, 2-
- the pharmaceutically acceptable acid addition salts as mentioned hereinabove are meant to comprise the therapeutically active non-toxic acid addition salt forms which the compounds of formula (I) are able to form.
- the compounds of formula (I) which have basic properties can be converted in their pharmaceutically acceptable acid addition salts by treating said base form with an appropriate acid.
- Appropriate acids comprise, for example, inorganic acids such as hydrohalic acids, e.g. hydrochloric or hydrobromic acid; sulfuric; nitric; phosphoric and the like acids; or organic acids such as, for example, acetic, propanoic, hydroxyacetic, lactic, pyruvic, oxalic, malonic, succinic (i.e.
- butanedioic acid maleic, fumaric, malic, tartaric, citric, methanesulfonic, ethanesulfonic, benzenesulfonic, p-toluenesulfonic, cyclamic, salicylic, p-amino- salicylic, pamoic and the like acids.
- acid addition salts also comprises the hydrates and the solvent addition forms which the compounds of formula (I) are able to form. Examples of such forms are e.g. hydrates, alcoholates and the like.
- stereochemically isomeric forms of compounds of formula (I), as used hereinbefore, defines all possible compounds made up of the same atoms bonded by the same sequence of bonds but having different three-dimensional structures which are not interchangeable, which the compounds of formula (I) may possess.
- chemical designation of a compound encompasses the mixture of all possible stereochemically isomeric forms which said compound may possess. Said mixture may contain all diastereomers and/or enantiomers of the basic molecular structure of said compound.
- All stereochemically isomeric forms of the compounds of formula (I) both in pure form or in admixture with each other are intended to be embraced within the scope of the present invention.
- X'-X 2 -X 3 is a trivalent radical of formula (x-1), (x-2), (x-3), (x-4) or (x-9) wherein each R 6 independently is hydrogen, d -4 alkyl, C ⁇ -4 alkyloxycarbonyl, amino or aryl and R 7 is hydrogen;
- R 1 is halo, C]. 6 alkyl or two R 1 substituents ortho to one another on the phenyl ring may independently form together a bivalent radical of formula (a-1);
- R 3 is halo or a radical of formula (b-1) or (b-3) wherein R 10 is hydrogen or a radical of formula -Alk-OR 13 .
- R 11 is hydrogen
- R 12 is hydrogen, d- 6 alkyl, d- 6 arkylcarbonyl, hydroxy, C ⁇ - 6 alkyloxy or mono- or di (C L ⁇ alky aminoC , - 6 alkylcarbonyl ;
- Alk is C ⁇ - 6 alkanediyl and
- R 13 is hydrogen; •
- R 4 is a radical of formula (c-1) or (c-2) wherein
- R 16 is hydrogen, halo or mono- or di(C 1 . alkyl)amino;
- R 17 is hydrogen or C t - 6 alkyl;
- aryl is phenyl
- R is C ⁇ - 4 alkyl, preferably 3-methyl, R is halo, preferably chloro, and most preferably 4-chloro, R 3 is a radical of formula (b-1) or (b-3), R 4 is a radical of formula (c-2), R 6 is C ⁇ - alkyl, R 9 is hydrogen, R 10 and R 11 are hydrogen and R 12 is hydrogen or hydroxy;
- the most preferred compounds of formula (I) are 7-[(4-fluorophenyl)(lH-imidazol-l-yl)methyl]-5-phenylimidazo[l,2-a]quinoline; ⁇ -(4-chlorophenyl)- ⁇ -(l-methyl-lH-imidazol-5-yl)-5-phenylimidazo[l,2-a]quinoline- 7-methanol; 5-(3-chlorophenyl)- ⁇ -(4-chlorophenyl)- ⁇ -( 1 -methyl- lH-imidazol-5-yl)- imidazo[l,2-a]quinoline-7-methanol; 5-(3-chlorophenyl)- ⁇ -(4-chlorophenyl)- -(l- methyl-lH-imidazol-5-yl)imidazo[l,2-a]quinoline-7-methanamine;5-(3-chlorophenyl)- -(4-
- the reaction may conveniently be carried out at elevated temperatures ranging from 80°C to reflux temperature.
- compounds of formula (1-2) can be prepared by reacting a compound of formula (VIII) with an intermediate of formula (VII). Said reaction can be performed in an appropriate solvent such as n-butanol at a temperature ranging between room temperature and reflux temperature.
- the intermediates of formula (VII) can be prepared by reacting an intermediate of formula (II) with N 2 H 4 . Said reaction can be JO-
- reaction may conveniently be carried out at a temperature ranging between room temperature and 100°C.
- Compounds of formula (1-2) wherein R is an amine, represented by compounds of formula (I-2-a) can be prepared by reacting an intermediate of formula (VII) with BrCN in a reaction-inert solvent such as methanol. The reaction may conveniently be carried out at a temperature ranging between 0°C and 100°C.
- the compounds of formula (1-3) can be prepared by reacting a compound of formula (X) with an intermediate of formula (II). Said reaction can be performed in an appropriate solvent such as 1-butanol at an elevated temperature ranging from 80°C to reflux temperature.
- the compounds of formula (1-4) can also be prepared by reacting an intermediate of formula (XVIII) with NaNO 2 in an acidic aqueous medium such as, for example HCl in water.
- the intermediates of formula (XI) can be prepared by reacting an intermediate of formula (XIII) with SeO 2 in a reaction-inert solvent such as dioxane. The reaction may conveniently be carried out at an elevated temperature ranging between room temperature and reflux temperature.
- Intermediates of formula (XIII) can generally be prepared by reacting an intermediate of formula (XIV) with 2-propanone in an acid solution such as a mixture of acetic acid and H 2 SO 4 . The reaction may conveniently be carried out at an elevated temperature ranging between room temperature and reflux temperature.
- compounds of formula (1-7) can be converted to the corresponding compounds of formula (1-6) by art-known oxidation procedures such as oxidation with MnO 2 in a reaction-inert solvent such as dichloromethane.
- compounds of formula (1-7) can be converted to compounds of formula (I-7-a) wherein >Y'-Y 2 is a trivalent radical of formula (y-3) or (y-1) and R 9 is other than hydrogen, by reacting these compounds of formula (1-7) with a reagent of formula R 9 -W 2 , wherein W 2 is an appropriate leaving group such as iodo, in a reaction-inert solvent such as dimethylformamide and in the presence of NaH.
- the reaction may conveniently be carried out at a temperature ranging between 0°C and room temperature.
- compounds of formula (1-8) can be converted to compounds of formula (I-8-b) wherein R 4 is halo, by reacting the compounds of formula (1-8) with a suitable halogenating agent such as thionyl chloride or phosphorus tribromide. Successively, the compounds of formula (I-8-b) can be treated with a reagent of formula H-NR n R 12 in a reaction-inert solvent, thereby yielding compounds of formula (I-8-c).
- the intermediates of formula (II) can be prepared by reacting an intermediate of formula (XV) with a suitable halogenating reagent such as POCl 3 .
- the intermediates of formula (XV) wherein >Y'-Y 2 is of formula (y-1) or (y-4) and R is of formula (c-2), can be prepared as described in WO 97/21701 from page 7 line 28 to page 16 line 3.
- the intermediates of formula (XV) wherein >Y'-Y 2 is of formula (y-2) or (y-3) and R 4 is of formula (c-1) or (c-2), can be prepared as described in WO 98/49157 from page 6 line 27 to page 13 line 14.
- intermediates of formula (II) wherein W 1 is chloro and R 3 is hydroxy represented by intermediates of formula (Il-a) can be prepared by reacting an intermediate of formula (XVI), wherein W 3 is a suitable leaving group such as Br, with an intermediate ketone of formula (XVII).
- This reaction is performed by converting the intermediate of formula (XVI) into an organometallic compound, by stirring it with a strong base such as butyl lithium and subsequently adding the intermediate ketone of formula (XVII).
- the hydroxy derivative can subsequently be converted into other intermediates wherein R 4 has another definition by performing art-known functional group transformations.
- Intermediates of formula (IV) can be prepared by reacting an intermediate of formula (XIV) with CH 3 CN in the presence of NaH and a suitable base such as pyridine.
- the reaction may conveniently be carried out at an elevated temperature ranging between 50°C and 100°C.
- the compounds of formula (I) and some of the intermediates have at least one stereogenic center in their structure.
- This stereogenic center may be present in a R or a S configuration.
- the compounds of formula (I) as prepared in the hereinabove described processes are generally racemic mixtures of enantiomers which can be separated from one another following art-known resolution procedures.
- the racemic compounds of formula (I) may be converted into the corresponding diastereomeric salt forms by reaction with a suitable chiral acid. Said diastereomeric salt forms are subsequently separated, for example, by selective or fractional crystallization and the enantiomers are liberated therefrom by alkali.
- An alternative manner of separating the enantiomeric forms of the compounds of formula (I) involves liquid chromatography using a chiral stationary phase.
- Said pure stereochemically isomeric forms may also be derived from the corresponding pure stereochemically isomeric forms of the appropriate starting materials, provided that the reaction occurs stereospecifically.
- said compound will be synthesized by stereospecific methods of preparation. These methods will advantageously employ enantiomerically pure starting materials.
- the compounds of formula (I), the pharmaceutically acceptable acid addition salts and stereoisomeric forms thereof have valuable pharmacological properties in that they surprisingly have both farnesyl protein transferase (FPTase) and geranylgeranyl transferase (GGTase) inhibitory effects.
- FPTase farnesyl protein transferase
- GTTase geranylgeranyl transferase
- This invention provides a method for inhibiting the abnormal growth of cells, including transformed cells, by administering an effective amount of a compound of the invention.
- Abnormal growth of cells refers to cell growth independent of normal regulatory mechanisms (e.g. loss of contact inhibition). This includes the abnormal growth of : (1) tumor cells (tumors) expressing an activated ras oncogene; (2) tumor cells in which the ras protein is activated as a result of oncogenic mutation of another gene; (3) benign and malignant cells of other proliferative diseases in which aberrant ras activation occurs.
- tumor cells tumor cells expressing an activated ras oncogene
- tumor cells in which the ras protein is activated as a result of oncogenic mutation of another gene
- benign and malignant cells of other proliferative diseases in which aberrant ras activation occurs.
- ras oncogenes not only contribute to the growth of tumors in vivo by a direct effect on tumor cell growth but also indirectly, i
- This invention also provides a method for inhibiting tumor growth by administering an effective amount of a compound of the present invention, to a subject, e.g. a mammal (and more particularly a human) in need of such treatment.
- this invention provides a method for inhibiting the growth of tumors expressing an activated ras oncogene by the administration of an effective amount of the compounds of the present invention.
- tumors which may be inhibited, but are not limited to, lung cancer (e.g. adenocarcinoma), pancreatic cancers (e.g. pancreatic carcinoma such as, for example exocrine pancreatic carcinoma), colon cancers (e.g.
- colorectal carcinomas such as, for example, colon adenocarcinoma and colon adenoma
- hematopoietic tumors of lymphoid lineage e.g. acute lymphocytic leukemia, B-cell lymphoma, Burkitt's lymphoma
- myeloid leukemias for example, acute myelogenous leukemia (AMIJ), thyroid follicular cancer, myelodysplastic syndrome (MDS), tumors of mesenchymal origin (e.g. fibrosarcomas and rhabdomyosarcomas), melanomas, teratocarcinomas, neuroblastomas, gliomas, benign tumor of the skin (e.g. keratoacanthomas), breast carcinoma, kidney carcinoma, ovary carcinoma, bladder carcinoma and epidermal carcinoma.
- lymphoid lineage e.g. acute lymphocytic leukemia, B-cell lymphoma, Burkitt's
- This invention may also provide a method for inhibiting proliferative diseases, both benign and malignant, wherein ras proteins are aberrantly activated as a result of oncogenic mutation in genes. With said inhibition being accomplished by the administration of an effective amount of the compounds described herein, to a subject in need of such a treatment.
- the benign proliferative disorder neuro- fibromatosis, or tumors in which ras is activated due to mutation or overexpression of tyrosine kinase oncogenes may be inhibited by the compounds of this invention.
- the compounds of present invention are particularly useful for the treatment of proliferative diseases, both benign and malignant, wherein the K-ras B isoform is activated as a result of oncogenic mutation.
- the present invention discloses the compounds of formula (I) for use as a medicine as well as the use of these compounds of formula (I) for the manufacture of a medicament for treating one or more of the above mentioned conditions.
- the subject compounds may be formulated into various pharmaceutical forms for administration purposes.
- compositions of this invention an effective amount of a particular compound, in base or acid addition salt form, as the active ingredient is combined in intimate admixture with a pharmaceutically acceptable carrier, which carrier may take a wide variety of forms depending on the form of preparation desired for administration.
- a pharmaceutically acceptable carrier which carrier may take a wide variety of forms depending on the form of preparation desired for administration.
- These pharmaceutical compositions are desirably in unitary dosage form suitable, preferably, for administration orally, rectally, percutaneously, or by parenteral injection.
- any of the usual pharmaceutical media may be employed, such as, for example, water, glycols, oils, alcohols and the like in the case of oral liquid preparations such as suspensions, syrups, elixirs and solutions; or solid carriers such as starches, sugars, kaolin, lubricants, binders, disintegrating agents and the like in the case of powders, pills, capsules and tablets. Because of their ease in administration, tablets and capsules represent the most advantageous oral dosage unit form, in which case solid pharmaceutical carriers are obviously employed.
- the carrier will usually comprise sterile water, at least in large part, though other ingredients, to aid solubility for example, may be included.
- Injectable solutions may be prepared in which the carrier comprises saline solution, glucose solution or a mixture of saline and glucose solution. Injectable suspensions may also be prepared in which case appropriate liquid carriers, suspending agents and the like may be employed.
- the carrier optionally comprises a penetration enhancing agent and/or a suitable wetting agent, optionally combined with suitable additives of any nature in minor proportions, which additives do not cause a significant deleterious effect to the skin. Said additives may facilitate the administration to the skin and/or may be helpful for preparing the desired compositions.
- These compositions may be administered in various ways, e.g., as a transdermal patch, as a spot-on, as an ointment.
- Dosage unit form as used in the specification and claims herein refers to physically discrete units suitable as unitary dosages, each unit containing a predetermined quantity of active ingredient calculated to produce the desired therapeutic effect in association with the required pharmaceutical carrier.
- dosage unit forms are tablets (including scored or coated tablets), capsules, pills, powder packets, wafers, injectable solutions or suspensions, teaspoonfuls, tablespoonfuls and the like, and segregated multiples thereof.
- an effective amount would be from 0.01 mg/kg to 100 mg/kg body weight, and in particular from 0.05 mg/kg to 10 mg/kg body weight. It may be appropriate to administer the required dose as two, three, four or more sub-doses at appropriate intervals throughout the day. Said sub-doses may be formulated as unit dosage forms, for example, containing 0.5 to 500 mg, and in particular 1 mg to 200 mg of active ingredient per unit dosage form.
- THF tetrahydrofuran
- DIPE diisopropylether
- DME 1,2- dimethoxyethane
- EtOAc ethylacetate
- Example Al Preparation of the intermediates Example Al a) A mixture of ( ⁇ )-6-[(4-fluorophenyl)(lH-imidazol-l-yl)methyl]-4-phenyl- 2(lH)-quinolinone (0.0253 mol) in phosphoryl chloride (30 ml) was refluxed for 1 hour. The mixture was evaporated till dryness and the product was used without further purification, yielding 10.4g (99%) of ( ⁇ )-2-chloro-6-[(4-fluorophenyl)(lH- imidazol-l-yl)methyl]-4-phenyl-quinoline (interm. 1).
- intermediate (27) intermediate (28) a) A mixture of (4-chlorophenyl)(4-nitrophenyl)-methanone (0.0382 mol), 1,2- ethanediol (0.0764 mol) and p-toluenesulfonic acid (0J9 mol) in toluene (150ml) was stirred and refluxed in a Dean Stark apparatus for 24h. The mixture was washed with K 2 CO 3 10% and then with water. The organic layer was dried, filtered off and evaporated, yielding (98%) of intermediate 19.
- 1,1 '-carbon ylbis-lH-imidazole (0.0055 mol) was added at room temperature to a solution of intermediate (7) (0.00367 mol) in T ⁇ F (30 ml) and the mixture was stirred at room temperature for 30 min. Ice and then water were added, and the mixture was extracted twice with EtOAc. The combined organic layer was separated, dried, filtered and the solvent was evaporated. The residue was taken up in C ⁇ 2CI2. The precipitate was filtered off and dried. The residue was crystallized from THF/di ethyl ether. The precipitate was filtered off and dried, yielding 0.85g (45%) of compound (22).
- Example B 15 n-Butyllithium (0.0129 mol) was added slowly at -70°C under N 2 flow to a solution of 1- methylimidazole (0.0129 mol) in T ⁇ F (25ml). The mixture was stirred for 30 min.
- Example B20 4-(3-chlorophenyl)- ⁇ 0 -(4-chlorophenyl)-2-hydrazino- ⁇ 6 -(l-methyl-lH-imidazol-5-yl)- 3,6-quinolinedimethanol (0.00371 mol) was added to ⁇ C1 IN (25 ml) and stirred at room temperature. A solution of NaNO 2 (0.00408 mol) in ⁇ 2 O (5 ml) was added dropwise and the resulting reaction mixture was stirred and refluxed for one hour.
- Fraction 2 was purified by column chromatography over silica gel (eluent: CH 2 Cl 2 /CH 3 OH7 NH-tOH 95/5/0.5; 20-45 ⁇ m). The pure fractions were collected and the solvent was evaporated. The residue was crystallized from CH 3 CN. The precipitate was filtered off and dried, yielding 0J7g of compound 80 (6%); mp. >250°C.
- Example C.2 "Ras-Transformed Cell Phenotype Reversion Assay”.
- the r ⁇ s-transformed cell phenotype reversion assay was performed essentially as described in WO 98/40383 , pages 34-36.
- Example C.3 "Farnesyl Protein Transferase Inhibitor Secondary Tumor Model”.
- the farnesyl protein transferase inhibitor secondary tumor model was used as described in WO 98/40383 , page 37.
- Example CJ " Geranylgeranyltransferase Type I Assay".
- GGTase I catalyzes the covalent attachment of a C-20 geranylgeranyl moiety derived from geranylgeranyl pyrophosphate to the K-ras oncogene product p21 ⁇ "ra ' s .
- the geranylgeranylation proceeds via formation of a thioether linkage to a single, specific cysteine residue contained in a cys-A-A-X motif wherein A represents neutral amino acids and X represents a C-terminal leucine or methionine.
- GGTase I Farnesylation of H,N, and K-ras isoforms by farnesyl protein transferase is required for activation and attachment of p21 ra5 to plasma membranes.
- the K-ras isoform which is the dominant isoform of ras in human tumors, is also isoprenylated by GGTase I. Therefore, inhibitors of GGTase I may inhibit the aberrant growth of K-ras transformed human tumors which are resistant to protein farnesyl transferase inhibitors.
- Kirsten virus transformed human osteosarcoma (KHOS) cells.
- the assay measures the covalent attachment of radioactivity from [-1H]-geranylgeranyl pyrophosphate to the K- ras peptide substrate biotinKKKKKKSKTLCVIM or biotinYRASNRSCAIL substrate.
- Control enzyme activity [CPM - ⁇ -geranylgeranyl peptide product in the presence of vehicle solvent]
- Test compound concentration 10 ⁇ M.
- Test compound % control activity (CPM - ⁇ - geranylgeranyl peptide product in the presence of test compound /control enzyme activity) X 100%)
- Standard Conditions Compounds were dissolved in DMSO at a concentration of 20 mM. Further dilutions were prepared in DMSO. The final concentration of DMSO in the assay medium was 10%. The compound concentration tested for screening was 10 ⁇ M.
- composition example Film-coated tablets Pr- v P-aratio ⁇ . pf tablet core
- the wet powder mixture is sieved, dried and sieved again.
- 100 g microcrystalline cellulose and 15 g hydrogenated vegetable oil The whole is mixed well and compressed into tablets, giving 10.000 tablets, each comprising 10 mg of a compound of formula (I).
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Abstract
This invention concerns compounds of formula (I), the pharmaceutically acceptable acid addition salts and the stereochemically isomeric forms thereof, wherein =X1-X2-X3- is a trivalent radical; ⊃Y1-Y2- is a trivalent radical; r and s are each independently 0, 1, 2, 3, 4 or 5; t is 0, 1, 2 or 3; each R?1 and R2¿ are independently hydroxy, halo, cyano, C¿1-6?alkyl, trihalomethyl, trihalomethoxy, C2-6alkenyl, C1-6alkyloxy, hydroxyC1-6alkyloxy, C1-6alkylthio, C1-6alkyloxyC1-6alkyloxy, C1-6alkyloxycarbonyl, aminoC1-6alkyloxy, mono- or di(C1-6alkyl)amino, mono- or di(C1-6alkyl)aminoC1-6alkyloxy, aryl, arylC1-6alkyl, aryloxy or arylC1-6alkyloxy, hydroxycarbonyl, C1-6alkyloxycarbonyl; or two R?1 or R2¿ on adjacent positions form together a bivalent radical; R3 is hydrogen, halo, C¿1-6?alkyl, cyano, haloC1-6alkyl, hydroxyC1-6alkyl, cyanoC1-6alkyl, aminoC1-6alkyl, C1-6alkyloxyC1-6alkyl, C1-6alkylthio-C1-6alkyl, aminocarbonylC1-6alkyl, hydroxycarbonyl, hydroxycarbonylC1-6alkyl, C1-6alkyloxycarbonylC1-6alkyl, C1-6alkylcarbonylC1-6alkyl, C1-6alkyloxycarbonyl, aryl, arylC1-6alkyloxyC1-6alkyl, mono- or di(C1-6alkyl)aminoC1-6alkyl, or a radical of formula -O-R?10, -S-R10 or -NR11R12; R4¿ is an optionally substituted imidazolyl; aryl is an optionally substituted phenyl or naphthalenyl; having farnesyl transferase and geranylgeranyl transferase inhibiting activity; their preparation, compositions containing them and their use as a medicine.
Description
1,2-ANNELATED QUINOLINE DERIVATIVES
The present invention is concerned with novel 1,2-annelated quinoline derivatives, the preparation thereof, pharmaceutical compositions comprising said novel compounds and the use of these compounds as a medicine as well as methods of treatment by administering said compounds.
Oncogenes frequently encode protein components of signal transduction pathways which lead to stimulation of cell growth and mitogenesis. Oncogene expression in cultured cells leads to cellular transformation, characterized by the ability of cells to grow in soft agar and the growth of cells as dense foci lacking the contact inhibition exhibited by non-transformed cells. Mutation and/or overexpression of certain oncogenes is frequently associated with human cancer. A particular group of oncogenes is known as ras which have been identified in mammals, birds, insects, mollusks, plants, fungi and yeasts. The family of mammalian ras oncogenes consists of three major members ("isoforms") : H-r s, K-ras and N-ras oncogenes. These ras oncogenes code for highly related proteins genetically known as p21 α5. Once attached to plasma membranes, the mutant or oncogenic forms of p21ra,y will provide a signal for the transformation and uncontrolled growth of malignant tumor cells. To acquire this transforming potential, the precursor of the p21 xs' oncoprotein must undergo an enzymatically catalyzed farnesylation of the cysteine residue located in a carboxyl-terminal tetrapeptide. Therefore, inhibitors of the enzymes that catalyzes this modification, i.e. farnesyl transferase, will prevent the membrane attachment of p21ra,s and block the aberrant growth of rα-j-transformed tumors. Hence, it is generally accepted in the art that farnesyl transferase inhibitors can be very useful as anticancer agents for tumors in which ras contributes to transformation.
The K-ras B isoform has been observed to be the dominant isoform which is mutated in human cancers, particular in colon (50% incidence) and pancreatic (90% incidence) cancers. However, it was also found that ras protein activation in the K-ras B isoform transformed cancers is resistant to inhibition of farnesyl transferase. The isoform confers resistance to farnesyl transferase inhibitors, but makes this isoform also substrate for geranylgeranyl transferase I. Therefore, inhibitors of geranylgeranyl transferase may inhibit the aberrant growth of K-ras transformed tumors which are resistant to farnesyl transferase inhibitors.
Since mutated oncogenic forms of ras are frequently found in many human cancers, most notably in more than 50 % of colon and pancreatic carcinomas (Kohl et al., Science, vol 260, 1834 - 1837, 1993), it has been suggested that farnesyl tranferase inhibitors can be very useful against these types of cancer.
In EP-0,371,564 there are described (lH-azol-1-ylmethyl) substituted quinoline and quinolinone derivatives which suppress the plasma elimination of retinoic acids. Some of these compounds also have the ability to inhibit the formation of androgens from progestines and or inhibit the action of the aromatase enzyme complex.
In WO 97/16443, WO 97/21701, WO 98/40383 and WO 98/49157, there are described 2-quinolone derivatives which exhibit farnesyl transferase inhibiting activity.
Unexpectedly, it has been found that the present novel 1,2-annelated quinoline compounds, bearing a nitrogen- or carbon-linked imidazole, show farnesyl protein transferase and geranylgeranyl transferase inhibiting activity.
The present invention concerns compounds of formula
=N-CR6=CR7- (x-1), =CR6-CR7=CR8- (x-6),
=N-N=CR6- (x-2), =CR6-N=CR7- (x-7),
=N-NΗ-C(=O)- (x-3), =CR6-NH-C(=O)- (x-8), or
=N-N=N- (x-4), =CR6-N=N- (x-9);
=N-CR6=N- (x-5), wherein each R6, R7 and R8 are independently hydrogen, C]- alkyl, hydroxy, Cι- alkyloxy, aryloxy, Cι-4alkyloxycarbonyl, hydroxyCι- alkyl, Cι-4alkyloxyCι- alkyl, mono- or di(Cι-4alkyl)aminoCι- alkyl, cyano, amino, thio, Cι- alkylthio, arylthio or aryl;
>Y'-Y2- is a trivalent radical of formula >CH-CHR9- (y-1),
>C=N- (y-2),
>CH-NR9- (y-3),or >C=CR9- (y-4); wherein each R9 independently is hydrogen, halo, halocarbonyl, aminocarbonyl, hydroxyCι-4alkyl, cyano, carboxyl,
Cι-4alkyloxy, Cι-4alkyloxyC1-4alkyl, Cι- alkyloxycarbonyl, mono- or di(Cι-4alkyl)amino, mono- or di(C1- 4alkyl)aminoCι-4alkyl, aryl; r and s are each independently 0, 1, 2, 3, 4 or 5; t is O, 1, 2 or 3; each R1 and R2 are independently hydroxy, halo, cyano, Cι_6alkyl, trihalomethyl, trihalomethoxy, C2-6alkenyl, C^alkyloxy, hydroxyCι-6alkyloxy, Cι-6alkylthio, C!-6alkyloxyC1-6alkyloxy, C^alkyloxycarbonyl, amino -ealkyloxy, mono- or di(Cι-6alkyl)amino, mono- or
aryl, aryl -ealkyl, aryloxy or arylCι-6alkyloxy, hydroxycarbonyl, Cι-6alkyloxycarbonyl, aminocarbonyl, amino -oalkyl, mono- or cti -δalky aminocarbonyl, mono- or di(C1-6alkyl)aminoCι-6alkyl; or two R1 or R2 substituents adjacent to one another on the phenyl ring may independently form together a bivalent radical of formula
-O-CH2-O- (a-1)-
-O-CH2-CH2-O- (a-2),
-O=CH=CH- (a-3),
-O-CH2-CH2- (a-4), -O-CH2-CH2- CH2- (a-5), or
-CH=CH-CH=CH- (a-6); R3 is hydrogen, halo, C,-6alkyl, cyano, halo -βalkyl, hydroxyC1-6alkyl, cyanoC,-6alkyl, aminoCι-6alkyl, C,-6alkyloxyC,-6alkyl, C1-6alkylthioC1-6alkyl, aminocarbonylCj-salkyl, hydroxycarbonyl, hydroxycarbonylCι-6alkyl, C1-6alkyloxycarbonylCι-6alkyl, d-ealkylcarbonylC^alkyl, Cι-6alkyloxycarbonyl, aryl, aryld-6alkyloxyCi-6alkyl, mono- or d -ealky aminoCi-βalkyl; or a radical of formula
-O-R10 (b-1),
-S-R10 ( -2), -NR"R12 (b-3)'
wherein R10 is hydrogen, Cι-6alkyl, Cι-6alkylcarbonyl, aryl, arylC,-6alkyl,
Cι-6alkyloxycarbonylC,-6alkyl, or a radical of formula -Alk-OR13 or -Alk-NR14R15; R11 is hydrogen, Cι-6alkyl, aryl or arylC^alkyl; R12 is hydrogen, C,-6alkyl, aryl, hydroxy, amino, C^alkyloxy,
aryld-ealkyl, CLβalkylcarbonylamino, mono- or di(Cι-6alkyl)amino, Cι-6alkylcarbonyl, aminocarbonyl, arylcarbonyl, haloCι-6alkylcarbonyl, arylCι-6alkylcarbonyl, C^alkyloxycarbonyl, CLsalkyloxyCLβalkylcarbonyl, mono- or di(C1-6alkyl)aminocarbonyl wherein the alkyl moiety may optionally be substituted by one or more substituents independently selected from aryl or Cι-3alkyloxycarbonyl, aminocarbonylcarbonyl, mono- or di(C1-6alkyl)aminoC1.6alkylcarbonyl, or a radical or formula -Alk-OR13 or -Alk-NR14R15; wherein Alk is Cι-6alkanediyl; R13 is hydrogen, Cι-6alkyl, Cι-6alkylcarbonyl, hydroxyC1-6alkyl, aryl or arylC,-6alkyl;
R14 is hydrogen, Cι-6alkyl, aryl or arylQ-ealkyl; R15 is hydrogen, C]-6alkyl, d-6alkylcarbonyl, aryl or arylQ-galkyl; R4 is a radical of formula
O-CH2-O- (a-1),
O-CH2-CH2-O- (a-2),
O=CH=CH- (a-3),
O-CH2-CH2- (a-4),
O-CH2-CH2- CH2- (a-5), or
CH=CH-CH=CH- (a-6);
R16 is hydrogen, halo, aryl, d-6alkyl, hydroxyCι-6alkyl, Cι-6alkyloxyd-6alkyl, d-6alkyloxy, C1-6alkylthio, amino, mono- or di(Cι-4alkyl)amino, hydroxycarbonyl, C,-5alkyloxycarbonyl, d-6alkylthioCι-6alkyl, Cι-6alkylS(O)Cι-6alkyl or d-6alkylS(O)2d-6alkyl; R16 may also be bound to one of the nitrogen atoms in the imidazole ring of formula (c-1), in which case the meaning of R16 when bound to the nitrogen is limited to hydrogen, aryl, C1-6alkyl, hydroxyC1-6alkyl, C,-6alkyloxyC1-6alkyl, - C,-6alkyloxycarbonyl, C,-6alkylS(O)C1-6alkyl or d-6alkylS(O)2d-6alkyl;
R17 is hydrogen, d-6alkyl, trifluoromethyl or di(Cι-4alkyl)aminosulfonyl.
As used in the foregoing definitions and hereinafter, halo is generic to fluoro, chloro, bromo and iodo; Ci^alkyl defines straight and branched chain saturated hydrocarbon radicals having from 1 to 4 carbon atoms such as, e.g. methyl, ethyl, propyl, butyl, 1-methylethyl, 2-methylpropyl and the like; Cι_6alkyl includes Cι_4alkyl and the higher homologues thereof having 5 to 6 carbon atoms such as, for example, pentyl, 2-methyl- butyl, hexyl, 2-methylpentyl and the like; Ci.galkanediyl defines bivalent straight and branched chained saturated hydrocarbon radicals having from 1 to 6 carbon atoms, such as, for example, methylene, 1,2-ethanediyl, 1,3-propanediyl, 1,4-butanediyl, 1,5-pentanediyl, 1,6-hexanediyl and the branched isomers thereof; C2-6 lkenyl defines straight and branched chain hydrocarbon radicals containing one double bond and having from 2 to 6 carbon atoms such as, for example, ethenyl, 2-propenyl, 3-butenyl,
2-pentenyl, 3-pentenyl, 3-methyl-2-butenyl, and the like. The term "S(O)" refers to a sulfoxide and "S(O)2" to a sulfon.
The pharmaceutically acceptable acid addition salts as mentioned hereinabove are meant to comprise the therapeutically active non-toxic acid addition salt forms which the compounds of formula (I) are able to form. The compounds of formula (I) which have basic properties can be converted in their pharmaceutically acceptable acid addition salts by treating said base form with an appropriate acid. Appropriate acids comprise, for example, inorganic acids such as hydrohalic acids, e.g. hydrochloric or hydrobromic acid; sulfuric; nitric; phosphoric and the like acids; or organic acids such as, for example, acetic, propanoic, hydroxyacetic, lactic, pyruvic, oxalic, malonic, succinic (i.e. butanedioic acid), maleic, fumaric, malic, tartaric, citric, methanesulfonic, ethanesulfonic, benzenesulfonic, p-toluenesulfonic, cyclamic, salicylic, p-amino- salicylic, pamoic and the like acids.
The term acid addition salts also comprises the hydrates and the solvent addition forms which the compounds of formula (I) are able to form. Examples of such forms are e.g. hydrates, alcoholates and the like.
The term stereochemically isomeric forms of compounds of formula (I), as used hereinbefore, defines all possible compounds made up of the same atoms bonded by the same sequence of bonds but having different three-dimensional structures which are not interchangeable, which the compounds of formula (I) may possess. Unless otherwise mentioned or indicated, the chemical designation of a compound encompasses the mixture of all possible stereochemically isomeric forms which said compound may possess. Said mixture may contain all diastereomers and/or enantiomers of the basic molecular structure of said compound. All stereochemically isomeric forms of the compounds of formula (I) both in pure form or in admixture with each other are intended to be embraced within the scope of the present invention.
Some of the compounds of formula (I) may also exist in their tautomeric forms. Such forms although not explicitly indicated in the above formula are intended to be included within the scope of the present invention.
Whenever used hereinafter, the term "compounds of formula (I)" is meant to include also the pharmaceutically acceptable acid addition salts and all stereoisomeric forms.
A group of interesting compounds consists of those compounds of formula (I) wherein one or more of the following restrictions apply :
• =X'-X2-X3 is a trivalent radical of formula (x-1), (x-2), (x-3), (x-4) or (x-9) wherein each R6 independently is hydrogen, d-4alkyl, Cι-4alkyloxycarbonyl, amino or aryl and R7 is hydrogen;
• >Y*-Y2- is a trivalent radical of formula (y-1), (y-2), (y-3), or (y-4) wherein each R9 independently is hydrogen, halo, carboxyl, C^alkyl or Cϊ^alkyloxycarbonyl;
• r is 0, 1 or 2;
• s is 0 or 1; • t is O;
• R1 is halo, C].6alkyl or two R1 substituents ortho to one another on the phenyl ring may independently form together a bivalent radical of formula (a-1);
• R2 is halo;
• R3 is halo or a radical of formula (b-1) or (b-3) wherein R10 is hydrogen or a radical of formula -Alk-OR13.
R11 is hydrogen;
R12 is hydrogen, d-6alkyl, d-6arkylcarbonyl, hydroxy, Cι-6alkyloxy or mono- or di (C Lβalky aminoC , -6alkylcarbonyl ; Alk is Cι-6alkanediyl and R13 is hydrogen; • R4 is a radical of formula (c-1) or (c-2) wherein
R16 is hydrogen, halo or mono- or di(C1. alkyl)amino; R17 is hydrogen or Ct-6alkyl;
• aryl is phenyl.
A particular group of compounds consists of those compounds of formula (I) wherein =X!-X2-X3 is a trivalent radical of formula (x-1), (x-2), (x-3) or (x-9), >Y1-Y2 is a trivalent radical of formula (y-2), (y-3) or (y-4), r is 0 or 1, s is 1, t is 0, R1 is halo, C(ι- )alkyl or forms a bivalent radical of formula (a-1), R is halo or Cι-4alkyl, R is hydrogen or a radical of formula (b-1) or (b-3), R4 is a radical of formula (c-1) or (c-2), R is hydrogen, C1-4alkyl or phenyl, R7 is hydrogen, R9 is hydrogen or Cι- alkyl, R is hydrogen or -Alk-OR13, R11 is hydrogen and R12 is hydrogen or C,.6alkylcarbonyl and R is hydrogen;
Preferred compounds are those compounds of formula (I) wherein =X1-X2-X3 is a trivalent radical of formula (x-1), >Y1-Y2 is a trivalent radical of formula (y-4), r is 0 or 1, s is 1, t is 0, R1 is halo, preferably chloro and most preferably 3-chloro, R2 is halo,
preferably 4-chloro or 4-fluoro, R3 is hydrogen or a radical of formula (b-1) or (b-3), R4 is a radical of formula (c-1) or (c-2), R6 is hydrogen, R7 is hydrogen, R9 is hydrogen, R10 is hydrogen, Rπ is hydrogen and R12 is hydrogen;
Other preferred compounds are those compounds of formula (I) wherein =X1-X2-X3 is a trivalent radical of formula (x-2) or (x-3), >Y1-Y2 is a trivalent radical of formula (y- 2), (y-3) or (y-4), r and s are 1, t is 0, R1 is halo, preferably chloro, and most preferably ι
3-chloro or R is Cι-4alkyl, preferably 3-methyl, R is halo, preferably chloro, and most preferably 4-chloro, R3 is a radical of formula (b-1) or (b-3), R4 is a radical of formula (c-2), R6 is Cι- alkyl, R9 is hydrogen, R10 and R11 are hydrogen and R12 is hydrogen or hydroxy;
The most preferred compounds of formula (I) are 7-[(4-fluorophenyl)(lH-imidazol-l-yl)methyl]-5-phenylimidazo[l,2-a]quinoline; α-(4-chlorophenyl)-α-(l-methyl-lH-imidazol-5-yl)-5-phenylimidazo[l,2-a]quinoline- 7-methanol; 5-(3-chlorophenyl)-α-(4-chlorophenyl)-α-( 1 -methyl- lH-imidazol-5-yl)- imidazo[l,2-a]quinoline-7-methanol; 5-(3-chlorophenyl)-α-(4-chlorophenyl)- -(l- methyl-lH-imidazol-5-yl)imidazo[l,2-a]quinoline-7-methanamine;5-(3-chlorophenyl)- -(4-chlorophenyl)-α-(l-methyl-lH-imidazol-5-yl)tetrazolo[l,5-a]quinoline-7- methanamine; 5-(3-chlorophenyl)-α-(4-chlorophenyl)- 1 -methyl-α-( 1 -methyl- 1H- imidazol-5-yl)-l,2,4-triazolo[4,3-a]quinoline-7-methanol; 5-(3-chlorophenyl)- -(4- chlorophenyl)- -(l-methyl-lH-imidazol-5-yl)tetrazolo[l,5-a]quinoline-7- methanamine; 5-(3-chlorophenyl)-α-(4-chlorophenyl)-α-(l -methyl- lH-imidazol-5- yl)tetrazolo[l,5-a]quinazoline-7-methanol; 5-(3-chlorophenyl)-α-(4-chlorophenyl)- 4,5-dihydro-α-(l-methyl-lH-imidazol-5-yl)tetrazolo[l,5-a]quinazoline-7-methanol; 5- (3-chlorophenyl)-α-(4-chlorophenyl)-α-(l-methyl-lH-imidazol-5-yl)tetrazolo[l,5- a]quinazoline-7-methanamine; 5-(3-chlorophenyl)-α-(4-chlorophenyl)-N-hydroxy- - (l-methyl-lH-imidazol-5-yl)tetrahydro[l,5-a]quinoline-7-methanamine; α-(4- chlorophenyl)-α-(l-methyl-lH-imidazol-5-yl)-5-(3-methylphenyl)tetrazolo[l,5- a]quinoline-7-methanamine; the pharmaceutically acceptable acid addition salts and the stereochemically isomeric forms thereof.
The compounds of formula (I) wherein =X!-X2-X3 is a trivalent radical of formula (x- 1) and R6 and R7 are hydrogen, represented by compounds of formula (1-1), can generally be prepared by reacting an intermediate of formula (II) with a reagent of formula (III) or a functional derivative thereof, wherein W1 is an appropriate leaving
group such as chloro, followed by an intramolecular cyclization which can be performed in a reaction-inert solvent such as xylene and in the presence of a suitable acid, for example acetic acid. The reaction may conveniently be carried out at elevated temperatures ranging from 80°C to reflux temperature.
Alternatively, compounds of formula (I) wherein =X'-X2-X3 is a trivalent radical of formula (x-1), >Y'-Y2 is a trivalent radical of formula (y-4), R9 is hydrogen and R6 and/or R7 are not hydrogen, represented by formula (I-l-a) can be prepared by reacting a compound of formula (IV) with a reagent of formula (V) followed by an intramolecular cyclization which can be performed in a reaction-inert solvent such as ethanol. The reaction may conveniently be carried out at temperatures ranging from room temperature to 80°C.
The compounds of formula (I) wherein =X!-X2-X3 is a trivalent radical of formula (x- 2), represented by compounds of formula (1-2), can generally be prepared by reacting a compound of formula (II) with an intermediate of formula (VI). Said reaction can be performed in an appropriate solvent such as 1-butanol at elevated temperatures ranging from 80°C to reflux temperature.
Alternatively, compounds of formula (1-2) can be prepared by reacting a compound of formula (VIII) with an intermediate of formula (VII). Said reaction can be performed in an appropriate solvent such as n-butanol at a temperature ranging between room temperature and reflux temperature. The intermediates of formula (VII) can be prepared by reacting an intermediate of formula (II) with N2H4. Said reaction can be
JO-
performed in a reaction-inert solvent such as dioxane. The reaction may conveniently be carried out at a temperature ranging between room temperature and 100°C.
Compounds of formula (1-2) wherein R is an amine, represented by compounds of formula (I-2-a) can be prepared by reacting an intermediate of formula (VII) with BrCN in a reaction-inert solvent such as methanol. The reaction may conveniently be carried out at a temperature ranging between 0°C and 100°C.
The compounds of formula (I) wherein =X'-X2-X3 is a trivalent radical of formula (x- 3), represented by compounds of formula (1-3), can generally be prepared by reacting an intermediate of formula (VII) with a compound of formula (IX) in a reaction-inert solvent such as tetrahydrofuran. The reaction may conveniently be carried out at a temperature ranging between 0°C and 50°C.
Alternatively, the compounds of formula (1-3) can be prepared by reacting a compound of formula (X) with an intermediate of formula (II). Said reaction can be performed in
an appropriate solvent such as 1-butanol at an elevated temperature ranging from 80°C to reflux temperature.
The compounds of formula (I) wherein =X]-X2-X3 is a trivalent radical of formula (x- 4), represented by compounds of formula (1-4), can generally be prepared by reacting an intermediate of formula (II) with NaN3 in a reaction-inert solvent such as N,N- dimethylformamide. The reaction may conveniently be carried out at an elevated temperature ranging between 60°C and 150°C.
Conversely, compounds of formula (1-7) can be converted to the corresponding compounds of formula (1-6) by art-known oxidation procedures such as oxidation with MnO2 in a reaction-inert solvent such as dichloromethane.
Also, compounds of formula (1-7) can be converted to compounds of formula (I-7-a) wherein >Y'-Y2 is a trivalent radical of formula (y-3) or (y-1) and R9 is other than hydrogen, by reacting these compounds of formula (1-7) with a reagent of formula R9-W2, wherein W2 is an appropriate leaving group such as iodo, in a reaction-inert solvent such as dimethylformamide and in the presence of NaH. The reaction may conveniently be carried out at a temperature ranging between 0°C and room temperature.
The compounds of formula (I) wherein R3 is a radical of formula (c-2) and R4 is hydroxy, represented by compounds of formula (1-8) can be converted to compounds of formula (I-8-a) wherein R4 is hydrogen, by submitting the compounds of formula (1-8) to appropriate reducing conditions such as stirring in acetic acid in the presence of formamide.
Further, compounds of formula (1-8) can be converted to compounds of formula (I-8-b) wherein R4 is halo, by reacting the compounds of formula (1-8) with a suitable halogenating agent such as thionyl chloride or phosphorus tribromide. Successively, the compounds of formula (I-8-b) can be treated with a reagent of formula H-NRnR12 in a reaction-inert solvent, thereby yielding compounds of formula (I-8-c).
The intermediates of formula (II) can be prepared by reacting an intermediate of formula (XV) with a suitable halogenating reagent such as POCl3.
The intermediates of formula (XV) wherein >Y*-Y2 is of formula (y-1) or (y-4) and R is of formula (c-1), can be prepared as described in WO 97/16443 from page 6 line 16 to page 16 line 3.
The intermediates of formula (XV) wherein >Y'-Y2 is of formula (y-1) or (y-4) and R is of formula (c-2), can be prepared as described in WO 97/21701 from page 7 line 28 to page 16 line 3.
The intermediates of formula (XV) wherein >Y'-Y2 is of formula (y-2) or (y-3) and R4 is of formula (c-1) or (c-2), can be prepared as described in WO 98/49157 from page 6 line 27 to page 13 line 14.
Alternatively, intermediates of formula (II) wherein W1 is chloro and R3 is hydroxy, represented by intermediates of formula (Il-a) can be prepared by reacting an intermediate of formula (XVI), wherein W3 is a suitable leaving group such as Br, with an intermediate ketone of formula (XVII). This reaction is performed by converting the intermediate of formula (XVI) into an organometallic compound, by stirring it with a strong base such as butyl lithium and subsequently adding the intermediate ketone of formula (XVII). The hydroxy derivative can subsequently be converted into other intermediates wherein R4 has another definition by performing art-known functional group transformations.
(XVI) (XVII)
Intermediates of formula (IV) can be prepared by reacting an intermediate of formula (XIV) with CH3CN in the presence of NaH and a suitable base such as pyridine. The reaction may conveniently be carried out at an elevated temperature ranging between 50°C and 100°C.
Intermediates of formula (XIV) can be prepared according to methods as described in WO 97/16443 and WO 97/21701.
The compounds of formula (I) and some of the intermediates have at least one stereogenic center in their structure. This stereogenic center may be present in a R or a S configuration.
The compounds of formula (I) as prepared in the hereinabove described processes are generally racemic mixtures of enantiomers which can be separated from one another following art-known resolution procedures. The racemic compounds of formula (I) may be converted into the corresponding diastereomeric salt forms by reaction with a suitable chiral acid. Said diastereomeric salt forms are subsequently separated, for
example, by selective or fractional crystallization and the enantiomers are liberated therefrom by alkali. An alternative manner of separating the enantiomeric forms of the compounds of formula (I) involves liquid chromatography using a chiral stationary phase. Said pure stereochemically isomeric forms may also be derived from the corresponding pure stereochemically isomeric forms of the appropriate starting materials, provided that the reaction occurs stereospecifically. Preferably if a specific stereoisomer is desired, said compound will be synthesized by stereospecific methods of preparation. These methods will advantageously employ enantiomerically pure starting materials.
The compounds of formula (I), the pharmaceutically acceptable acid addition salts and stereoisomeric forms thereof have valuable pharmacological properties in that they surprisingly have both farnesyl protein transferase (FPTase) and geranylgeranyl transferase (GGTase) inhibitory effects.
Furthermore, the compounds of formula (I), in particular those compounds of formula
( (II)) wwhheerreeiinn =X1-X2-X3 is a trivalent radical of formula (x-4), display potent GGTase inhibition.
Other compounds of formula (I) are found to be particularly usefull for the inhibition of FPTase activity.
This invention provides a method for inhibiting the abnormal growth of cells, including transformed cells, by administering an effective amount of a compound of the invention. Abnormal growth of cells refers to cell growth independent of normal regulatory mechanisms (e.g. loss of contact inhibition). This includes the abnormal growth of : (1) tumor cells (tumors) expressing an activated ras oncogene; (2) tumor cells in which the ras protein is activated as a result of oncogenic mutation of another gene; (3) benign and malignant cells of other proliferative diseases in which aberrant ras activation occurs. Furthermore, it has been suggested in literature that ras oncogenes not only contribute to the growth of tumors in vivo by a direct effect on tumor cell growth but also indirectly, i.e. by facilitating tumor-induced angiogenesis (Rak. J. et al, Cancer Research, 55, 4575-4580, 1995). Hence, pharmacologically targeting mutant ras oncogenes could conceivably suppress solid tumor growth in vivo, in part, by inhibiting tumor-induced angiogenesis.
This invention also provides a method for inhibiting tumor growth by administering an
effective amount of a compound of the present invention, to a subject, e.g. a mammal (and more particularly a human) in need of such treatment. In particular, this invention provides a method for inhibiting the growth of tumors expressing an activated ras oncogene by the administration of an effective amount of the compounds of the present invention. Examples of tumors which may be inhibited, but are not limited to, lung cancer (e.g. adenocarcinoma), pancreatic cancers (e.g. pancreatic carcinoma such as, for example exocrine pancreatic carcinoma), colon cancers (e.g. colorectal carcinomas, such as, for example, colon adenocarcinoma and colon adenoma), hematopoietic tumors of lymphoid lineage (e.g. acute lymphocytic leukemia, B-cell lymphoma, Burkitt's lymphoma), myeloid leukemias (for example, acute myelogenous leukemia (AMIJ), thyroid follicular cancer, myelodysplastic syndrome (MDS), tumors of mesenchymal origin (e.g. fibrosarcomas and rhabdomyosarcomas), melanomas, teratocarcinomas, neuroblastomas, gliomas, benign tumor of the skin (e.g. keratoacanthomas), breast carcinoma, kidney carcinoma, ovary carcinoma, bladder carcinoma and epidermal carcinoma.
This invention may also provide a method for inhibiting proliferative diseases, both benign and malignant, wherein ras proteins are aberrantly activated as a result of oncogenic mutation in genes. With said inhibition being accomplished by the administration of an effective amount of the compounds described herein, to a subject in need of such a treatment. For example, the benign proliferative disorder neuro- fibromatosis, or tumors in which ras is activated due to mutation or overexpression of tyrosine kinase oncogenes, may be inhibited by the compounds of this invention.
The compounds of present invention are particularly useful for the treatment of proliferative diseases, both benign and malignant, wherein the K-ras B isoform is activated as a result of oncogenic mutation.
Hence, the present invention discloses the compounds of formula (I) for use as a medicine as well as the use of these compounds of formula (I) for the manufacture of a medicament for treating one or more of the above mentioned conditions.
In view of their useful pharmacological properties, the subject compounds may be formulated into various pharmaceutical forms for administration purposes.
To prepare the pharmaceutical compositions of this invention, an effective amount of a particular compound, in base or acid addition salt form, as the active ingredient is
combined in intimate admixture with a pharmaceutically acceptable carrier, which carrier may take a wide variety of forms depending on the form of preparation desired for administration. These pharmaceutical compositions are desirably in unitary dosage form suitable, preferably, for administration orally, rectally, percutaneously, or by parenteral injection. For example, in preparing the compositions in oral dosage form, any of the usual pharmaceutical media may be employed, such as, for example, water, glycols, oils, alcohols and the like in the case of oral liquid preparations such as suspensions, syrups, elixirs and solutions; or solid carriers such as starches, sugars, kaolin, lubricants, binders, disintegrating agents and the like in the case of powders, pills, capsules and tablets. Because of their ease in administration, tablets and capsules represent the most advantageous oral dosage unit form, in which case solid pharmaceutical carriers are obviously employed. For parenteral compositions, the carrier will usually comprise sterile water, at least in large part, though other ingredients, to aid solubility for example, may be included. Injectable solutions, for example, may be prepared in which the carrier comprises saline solution, glucose solution or a mixture of saline and glucose solution. Injectable suspensions may also be prepared in which case appropriate liquid carriers, suspending agents and the like may be employed. In the compositions suitable for percutaneous administration, the carrier optionally comprises a penetration enhancing agent and/or a suitable wetting agent, optionally combined with suitable additives of any nature in minor proportions, which additives do not cause a significant deleterious effect to the skin. Said additives may facilitate the administration to the skin and/or may be helpful for preparing the desired compositions. These compositions may be administered in various ways, e.g., as a transdermal patch, as a spot-on, as an ointment. It is especially advantageous to formulate the aforementioned pharmaceutical compositions in dosage unit form for ease of administration and uniformity of dosage. Dosage unit form as used in the specification and claims herein refers to physically discrete units suitable as unitary dosages, each unit containing a predetermined quantity of active ingredient calculated to produce the desired therapeutic effect in association with the required pharmaceutical carrier. Examples of such dosage unit forms are tablets (including scored or coated tablets), capsules, pills, powder packets, wafers, injectable solutions or suspensions, teaspoonfuls, tablespoonfuls and the like, and segregated multiples thereof.
Those skilled in the art could easily determine the effective amount from the test results presented hereinafter. In general it is contemplated that an effective amount would be from 0.01 mg/kg to 100 mg/kg body weight, and in particular from 0.05
mg/kg to 10 mg/kg body weight. It may be appropriate to administer the required dose as two, three, four or more sub-doses at appropriate intervals throughout the day. Said sub-doses may be formulated as unit dosage forms, for example, containing 0.5 to 500 mg, and in particular 1 mg to 200 mg of active ingredient per unit dosage form.
The following examples are provided for purposes of illustration.
Experimental part
Hereinafter "THF" means tetrahydrofuran, "DIPE" means diisopropylether, "DME" means 1,2- dimethoxyethane and "EtOAc" means ethylacetate.
A. Preparation of the intermediates Example Al a) A mixture of (±)-6-[(4-fluorophenyl)(lH-imidazol-l-yl)methyl]-4-phenyl- 2(lH)-quinolinone (0.0253 mol) in phosphoryl chloride (30 ml) was refluxed for 1 hour. The mixture was evaporated till dryness and the product was used without further purification, yielding 10.4g (99%) of (±)-2-chloro-6-[(4-fluorophenyl)(lH- imidazol-l-yl)methyl]-4-phenyl-quinoline (interm. 1). b) A mixture of intermediate (1) (0.0251 mol) in 2,2-dimethoxyethylamine (20 ml) was stirred at 120°C for 12 hours. The mixture was poured into ice water and extracted with CΗ2CI2. The organic layer was dried (MgSO4) and evaporated till dryness. The oily residue (21g) was purified by column chromatography over silica gel. The pure fractions were collected and evaporated, yielding lOg (83%) of (±)-N-(2,2- dimethoxyethyl)-6-[(4-fluorophenyl)(lH-imidazol-l-yl)methyl]-4-phenyl-2- quinolinamine (interm. 2).
Example A2
a) Preparation of intermediate (3)
Sodium hydride (0.0384 mol) was added portionwise to a mixture of ( ±)-[2-amino-5- [(4-chlorophenyl)hydroxy(l-methyl-lH-imidazol-5-yl)methyl]phenyl](3-chloro- phenyl)methanone (0.00961 mol) and acetonitrile (0.058 mol) in pyridine (30ml). The mixture was stirred at 90°C for 6 hours and then cooled. Η2O was added. The solvent was evaporated. The residue was taken up in CH2CI2. The organic solution was
washed with H2O, dried (MgSO4), filtered and the solvent was evaporated. The residue (6Jg) was purified by column chromatography over silica gel. The pure fractions were collected and the solvent was evaporated, yielding 2.9g (63%) of intermediate 3.
b) Preparation of intermediate (4)
Ethyl bromopyruvate (0.0023 mol) was added to a mixture of intermediate (3) (0.0019 mol) in DME (5 ml). The mixture was stirred at room temperature for 19 hours. A gum was filtered off, washed with diethyl ether and used without further purification, yielding intermediate (4).
Example A3
A mixture of (±)-6-[(4-chlorophenyl)-lH-imidazol-l-ylmethyl]-4-phenyl-2(lH)-quino- linone (0.022 mol) in phosphoryl chloride (100ml) was stirred and refluxed for 2 hours. The mixture was evaporated in vacuo, the residue was taken up in CΗ2CI2 and basified with K2CO3 (10%). The organic layer was dried (MgSO4), filtered off and evaporated. The product was used without further purification, yielding 8 g (85%) of (±)-2-chloro-6- [(4-chlorophenyl)-lH-imidazol-l-ylmethyl]-4-phenylquinoline (interm. 5).
Example A4
A mixture of intermediate (6) (0.0242 mol) in hydrazine hydrate (120 ml) and dioxane (240 ml) was stirred at 70°C overnight and then brought to room temperature. Η2O was added and the mixture was extracted with CH2CI2. The organic layer was separated, washed with a saturated NaCl solution, dried (MgSO4), filtered and the solvent was evaporated, yielding 11.8g of intermediate 7.
Example A5
intermediate 8 intermediate 9
A solution of butyllithium in hexane (1.6 M) (74.4 ml) was added dropwise at -70°C under N2 flow to a mixture of 1-methylimidazole (0J 19 mol) in THF (200 ml). The mixture was stirred at -70°C for 30 minutes. Chlorotriethylsilane (0J19 mol) was added. The mixture was brought slowly to 10°C and cooled again to -70°C. A solution of butyllithium in hexane (1.6 M) (74.4ml) was added dropwise. The mixture was stirred at -70°C for 1 hour, brought to -15°C and cooled again to -70°C. A mixture of intermediate (8) (0.052 mol) in THF (200 ml) was added dropwise. The mixture was stirred at -70°C for 30 min, hydrolized, extracted with EtOAc and decanted. The organic layer was dried (MgSO4), filtered and the solvent was evaporated. The residue was purified by column chromatography over silica gel. The pure fractions were collected and the solvent was evaporated, yielding 12g (46.5%) of intermediate (9).
Example A6
a) Preparation of intermediate (10)
A mixture of (±)-[2-amino-5-[(4-chlorophenyl)hydroxy(l-methyl-lH-imidazol-5- yl)methyl]phenyl](3-chlorophenyl)methanone (0.0415 mol) and 2-propanone (0J24 mol) in sulfuric acid (0.6 ml) and acetic acid (55 ml) was stirred and refluxed overnight, brought to room temperature, poured out on ice, basified with NΗ4OΗ and extracted with CH2CI2. The organic layer was separated, dried (MgSO4), filtered and the solvent was evaporated. The residue (30 g) was purified by column chromatography over silica gel. The pure fractions were collected and the solvent was evaporated, yielding 12g (60%) of product. Part of this fraction (2g) was crystallized from CH3CN. The precipitate was filtered off and dried, yielding 1.25g (37.5%) of intermediate (10).
b) Preparation of intermediate (11)
A mixture of intermediate (10) (0.0116 mol) and selenium dioxide (0.0116 mol) in dioxane (55 ml) and water (5.5 ml) was stirred and refluxed for 3 hours. The mixture was cooled, filtered over celite, washed with CH2CI2, dried (MgSO4), filtered and the solvent was evaporated, yielding 5.66g of intermediate (11).
Example A7
Butyllithium in hexane (1.6 M) (5.3 ml) was added dropwise at -70°C to a mixture of intermediate (12) (0.0071 mol) in tetrahydrofuran (25 ml). The mixture was stirred at -70°C for 30 minutes. A solution of intermediate (13) (0.0078 mol) in THF (10ml) was added dropwise. The mixture was stirred for 1 hour, hydrolized and extracted with EtOAc. The organic layer was separated, dried (MgSO4), filtered and the solvent was evaporated till dryness. The residue (3.9g) was purified by column chromatography over silica gel. Two pure fractions were collected and their solvents were evaporated, yielding 1.3g (65%; starting material (intermediate 13) and 0.71g (19%) of intermediate (14). Example A8
Preparation of intermediate (15)
A mixture of (4-chlorophenyl)[2-chloro-4-(3-chlorophenyl)-6-quinolinyl]methanone (0.016 mol) and NaN3 (0.024 mol) in DMF (50ml) was stirred at 100°C for 8 hours, brought to room temperature and poured out on ice. The precipitate was filtered off, washed with H2O and taken up in CH2C1 . The organic layer was separated, dried,
filtered and the solvent was evaporated. The residue was taken up in CH3CN. The precipitate was filtered off and dried, yielding 5Jg of intermediate (15) (76%).
Example A9
Preparation of intermediate (16)
A mixture of (4-chlorophenyl)[2-chloro-4-(3-chlorophenyl)-6-quinolinyl]methanone monohydrochloride (0.0349 mol) and hydrazinecarboxaldehyde (0.0524 mol) in 1-butanol (180ml) was stirred and refluxed for the weekend. The solvent was evaporated. THF (100ml) and HCl 3N (200ml) were added. The mixture was stirred and refluxed for 3 hours. The mixture was cooled, poured out on ice, basified with NH4OH, filtered over celite, washed with EtOAc and decanted. The organic layer was dried (MgSO4), filtered and the solvent was evaporated. The residue (11.8g) was purified by column chromatography over silica gel (eluent: CH2Cl2/CH3OH/NH4OH 97/3/OJ; 20-45 μm). The pure fractions were collected and the solvent was evaporated. Yielding: 5g of intermediate 16 (34%).
Example A10
a) Preparation of intermediate (17)
A mixture of 6-bromo-2-chloro-4-(3-chlorophenyl)quinoline (0.0276 mol) in THF (30ml) was cooled to -70°C under N2 flow. BuLi 1.6N in hexane (0.033 mol) was added dropwise at -70°C. The mixture was stirred at -70°C for 1 hour. A solution of 2,4-difluorobenzaldehyde (0.0276 mol) in THF (100ml) was added dropwise at -70°C. The mixture was stirred at -70°C for 1 hour, hydrolized cold and extracted with EtOAc. The organic layer was separated, washed with H2O, dried (MgSO ), filtered and the solvent was evaporated. The residue was purified by column chromatography over silica gel (eluent: CH2Cl2/CH3OH 99.5/0.5; 20-45 μm). The pure fractions were collected and the solvent was evaporated. Yielding: 5.2g of intermediate (17) (46%).
b) Preparation of intermediate (18)
Mnθ2 (0.0374 mol) was added to a mixture of intermediate (17) (0.0125 mol) in dioxane (50ml). The mixture was stirred at 80°C overnight, brought to room temperature, filtered over celite and washed with CH2C12. The filtrate was evaporated. Yielding: 5g of intermediate (18) (96%).
Example Al l
Example A12
Intermediate 30 Intermediate 32 Intermediate 33 a) A mixture of intermediate 29, prepared analogous to example Al (0.0727 mol), in acetic acid (90ml) and xylene (300ml) was stirred and for 72h. The solvent was evaporated. The residue was taken in CH2C12, K2CO3 10% was added and filtered over celite. The organic layer was decanted, dried, filtered and the solvent was evaporated. The residue was purified by column chromatography over silica gel (eluent: CH2Ci2/CH OH 99/1). The pure fractions were collected and the solvent was evaporated. The residue was recrystallized from CH3CN. The precipitate was filtered off and dried, yielding 6.7g (56%) intermediate 30. b) NaBHi (0.0086 mol) was added portionwise at 10°C to a solution of intermediate 30 (0.00719 mol) in methanol (30ml) and THF (20ml). The mixture was stirred at °C for 15 min. Water was added and the mixture was concentrated. The concentrate was taken up in CH2C12. The organic layer was separated, washed with water, dried, filtered and the solvent was evaporated. The residue was crystallized from 2-propanone. The precipitate was filtered off and dried, yielding 1.45g (48%) of intermediate 31. c) A mixture of intermediate 30 (0.0096 mol) in formamide (19ml) and acetic acid (20ml) was stirred at 160°C for 48 hours. The mixture was cooled. Ice was added. The mixture was extracted with CH2C12 and decanted. The organic layer was dried, filtered and the solvent was evaporated, yielding 4.2g of intermediate 32.
d) A mixture of intermediate 32 (0.0096 mol) in HCl 3N (60ml) and 2-propanol (60ml) was stirred at 80°C for 2.5 hours. The mixture was poured out on ice, basified with NFLjOH and extracted with CH2CI2. The organic layer was separated, dried, filtered and the solvent was evaporated. The residue was purified by column chromatography over silica gel (eluent: CH2Cl2/CH3OH/NH4OH 98/2/0J). The pure fractions were collected and the solvent was evaporated. The residue was crystallized from CH3CN and DIPE. The precipitate was filtered off and dried, yielding 1.15g (29%) of intermediate 33.
Example A13
B. Preparation of the final compounds.
Example B 1
A mixture of intermediate (2) (0.0207 mol) in acetic acid (10 ml) and mixed xylenes
(100 ml) was stirred and refluxed for 12 hours and cooled. The mixture was evaporated and the residue was taken up in water, basified with NaOH (2N) and extracted with
CH2CI2. The residue was purified by column chromatography over silica gel. The pure fractions were collected and evaporated. The residue was converted into the ethanedioic acid salt (2:3) in C2H5OH/CH3OH/2-propanone, yielding 3.5g (30%) of (±)-7-[(4-fluorophenyl)(lH-imidazol-l-yl)methyl]-5-phenylimidazo[l,2-a]quinoline ethanedioate(2:3).hemihydrate; mp. 204.3°C (comp. 3).
Example B2
Preparation of compound (95)
Example B3
A mixture of intermediate (5) (0.029 mol) and formylhydrazine (0.043 mol) in 1-butanol (150 ml) was stirred and refluxed for 48 hours. The mixture was evaporated, the residue was taken up in CH2CI2 and washed with water. The organic layer was dried, filtered off and evaporated. The residue was purified by column chromatography over silica gel. The pure fractions were collected and evaporated. The residue was dissolved in 2-propanone and converted into the ethanedioic acid salt (2:3) yielding 4.4g (26J%>) of (±)-7-[(4-chlorophenyl)-lHJmidazol-l-ylmethyl]-5-phenyl[l,2,4]- triazolo[4,3-a]quinoline ethanedioate(2:3).hemihydrate (comp. 5).
Example B4
A mixture of intermediate (7) (0.0071 mol) and triethyl orthoacetate (0.0086 mol) in n-butanol (35ml) was stirred at 100°C overnight. The solvent was evaporated. The residue was taken up in CΗ2CI2, washed with H2O and with a saturated NaCl solution, dried, filtered and the solvent was evaporated. The residue was purified by column chromatography over silica gel. The pure fractions were collected and the solvent was evaporated. The residue was crystallized from 2-propanone. The precipitate was filtered off and dried yielding 1.95g (53%) of (±)-5-(3-chlorophenyl)-α-(4- chlorophenyl)-l-methyl- -(l-methyl-lH-imidazol-5-yl)-l,2J-triazolo[4,3-a]quinoline- 7-methanol (comp. 19).
Example B5
Preparation of compound (20)
Example B6
Preparation of compound (22)
Example B7
A mixture of intermediate (5) (0.029 mol) and ethyl carbazate (0.0436 mol) in
1-butanol (150 ml) was stirred and refluxed for one night. The mixture was evaporated in vacuo, the residue was taken up in CH2Cl2 and washed with water. The organic layer was dried, filtered off and evaporated. The residue was purified by column chromatography over silica gel. The pure fractions were collected and evaporated. The residue was dissolved in 2-propanone and converted into the ethanedioic acid salt (1:1) yielding lg (6.3%) of (±)-7-[(4-chlorophenyl)-lHJmidazol-l-ylmethyl]-5- ρhenyl[l,2,4]triazolo[4,3-a]quinolin-l(2H)-one ethanedioate(l:l).hemihydrate; mp. 198.3°C (comp. 7).
Example B8
A mixture of intermediate (9) (0.006 mol) and sodium azide (0.018 mol) in DMF (20 ml) was stirred at 140°C for 4 hours. The mixture was cooled to room temperature and
poured out into ice water. The precipitate was filtered off, washed with H2O and taken up in CH2CI2. The organic solution was dried, filtered and the solvent was evaporated. The residue was crystallized from CH3CN and 2-propanone. The precipitate was filtered off and dried yielding 1.2g (38.2%)) of (±)-5-(3-chlorophenyl)-α-(4- chlorophenyl)-α-(l-methyl-lH-imidazol-5-yl)tetrazolo[l,5-a]quinazoline-7-methanol; mp. 139°C (comp. 29).
Example B9
A mixture of intermediate (11) (0.0116 mol) and p-toluenesulfonhydrazide
(0.0128 mol) in CΗ3OΗ (60 ml) was stirred at 60°C for 2 hours and then brought to room temperature. H2O was added. The mixture was extracted with CH2CI2. The organic layer was separated, dried, filtered and the solvent was evaporated. The residue was purified by column chromatography over silica gel. Two pure fractions were collected and their solvents were evaporated. The desired fraction was crystallized from 2-propanone and CH3CN. The precipitate was filtered off and dried yielding 1.25 g (21%) of (±)-5-(3-chlorophenyl)-α-(4-chlorophenyl)- -(l -methyl- lH-imidazol-5-yl)- [l,2,3]triazolo[l,5-a]quinoline-7-methanol; mp. 222°C (comp. 26).
Example B10
A mixture of compound (29) (0.008 mol) in methanol (60ml) was cooled to 5°C. Sodium tetrahydroborate (0.008 mol) was added portionwise. The mixture was stirred at 5°C for 1 hour, hydrolized, extracted with CΗ2C12 and decanted. The organic layer was dried, filtered and the solvent was evaporated. The residue was crystallized from 2- propanone. The precipitate was filtered off and dried yielding 1.8g (44.6%) of (±)-5-(3- chlorophenyl)-α-(4-chlorophenyl)-4,5-dihydro-α-(l -methyl- lH-imidazol-5- yl)tetrazolo[l,5-a]quinazoline-7-methanol; mp. 212°C (comp. 30). Example Bl l
A dispersion of sodium hydride (80%) in a mineral oil (0.0083 mol) was added at 5°C under N2 flow to a mixture of intermediate (10) (0.007 mol) in DMF (33 ml). The mixture was stirred at 5°C for 30 min. Iodomethane (0.008 mol) was added. The mixture was stirred at 5°C for 30 minutes and then hydrolized. The precipitate was filtered off, washed with Η2O and taken up in CH2CI2. The organic solution was dried, filtered and the solvent was evaporated. The residue was purified by column chromatography over silica gel. The pure fractions were collected and the solvent was evaporated. The residue was crystallized from CH3CN and DIPE. The precipitate was filtered off and dried, yielding 0.8g (22%) of (±)-5-(3-chlorophenyl)- -(4-
chlorophenyl)-4,5-dihydro-4-methyl- -(l-methyl-lH-imidazol-5-yl)tettazolo[l,5- a]quinazoline-7-methanol; mp. 235°C (comp. 33).
Example B 12
Preparation of compound (94)
A mixture of (±)-5-(3-chlorophenyl)-α-(4-chlorophenyl)- -(l-methyl-lH-imidazol-5- yl)tetrazolo[l,5-a]quinoline-7-methanol (0.005 mol) in formamide (10 ml) and acetic acid (20 ml) was stirred at 160°C for 5 hours, poured out on ice, basified with NΗ4OΗ and extracted with CH2θ2. The organic layer was separated, dried, filtered and the solvent was evaporated. The residue was purified by column chromatography over silica gel. The pure fractions were collected and the solvent was evaporated. The residue was crystallized from CH3CN and diethyl ether. The precipitate was filtered off and dried yielding 0.84g (35%) of compound (94); mp. 166°C
Example B 13
Preparation of compound (31)
Compound (29) (0.006 mol) was added at a low temperature to thionyl chloride (30 ml). The mixture was stirred at 40°C for 2 hours. The solvent was evaporated, yielding compound (31).
Example B 14
A mixture of 2-propanol and NH3 (35 ml) was added dropwise quickly at 0°C to a mixture of compound (31) (0.006 mol) in THF (35 ml). The mixture was stirred at 5°C for 30 min and then brought to room temperature. The solvent was evaporated. The residue was taken up in CH2C12 and H2O and the mixture was decanted. The organic layer was dried, filtered and the solvent was evaporated. The residue was purified by column chromatography over silica gel. The pure fractions were collected and the solvent was evaporated. The residue was crystallized from CH2CI2 and DIPE. The precipitate was filtered off and dried yielding 0.6g (20%) of (±)-5-(3-chlorophenyl)-α-
(4-chlorophenyl)-α-(l-methyl-lH-imidazol-5-yl)tetrazolo[l,5-a]quinazoline-7- methanamine; mp. 159°C (comp. 32).
Example B 15 n-Butyllithium (0.0129 mol) was added slowly at -70°C under N2 flow to a solution of 1- methylimidazole (0.0129 mol) in TΗF (25ml). The mixture was stirred for 30 min.
Chlorotriethylsilane (0.0129 mol) was added. The mixture was allowed to warm to room temperature and then cooled to -70°C. n-Butyllithium (0.0129 mol) was added. The mixture was stirred at -70°C for 1 hour, then allowed to warm to -15°C and cooled to - 70°C. A solution of (±)-α-(4-chlorophenyl)-5-phenylimidazo[l,2-a]quinoline-7- methanone (0.0107 mol) in TΗF (12 ml) was added. The mixture was stirred at -70°C for 1 hour. Water was added. The mixture was extracted with EtOAc. The organic layer was separated, dried, filtered and the solvent was evaporated. The residue was purified by column chromatography over silica gel. The pure fractions were collected and the solvent was evaporated. The residue was crystallized from 2-propanone. The precipitate was filtered off and dried, yielding 0.9g (18%) of (±)-α-(4-chlorophenyl)-α-(l -methyl- 1H- imidazol-5-yl)-5-phenylimidazo[l,2-a]quinoline-7-methanol (compound 11).
Example B 16
Preparation of compound (25)
A mixture of intermediate 28 (0.00286 mol) and lHJmidazole (0.017 mol) in CΗ3CN (20ml) was stirred and refluxed for 48 hours and then brought to room temperature. H2O was added. The mixture was extracted with CH2CI2. The organic layer was separated, dried, filtered and the solvent was evaporated. The residue was purified by column over silica gel (eluent: CH^yCHsOH/NKUOH 98/2/0.1). The pure fractions were collected and the solvent was . The residue was crystallized from CH3CN and DIPE. The precipitate was filtered off and dried, yielding 0.55g compound 25 (40%). Example B 17
Preparation of compound (144)
A mixture of compound 53 (0.00464 mol) in SOCl2 (30ml) was stirred at 60°C for 6 hours. The solvent was evaporated, yielding compound 76.
Example B 19
A mixture of compound 16 (0.0022 mol) in 1,2-ethanediol (15ml) and H2SO4 (cone.) (5 drops) was stirred and refluxed at 125°C for 6 hours. K-2CO3 10% was added and the mixture was extracted with CH2C12. The organic layer was separated, dried, filtered, and the solvent was evaporated. The residue was purified by column chromatography over silica gel (eluent: toluene/2-propanol/NH4OH 88/12/0.8). The pure fractions were collected and the solvent was evaporated. The residue was converted into the ethanedioic acid salt (1: 1) in 2-propanone and crystallized from CH3CN/2-propanone. The precipitate was filtered off, washed with diethyl ether and dried, yielding 0.5 g of compound 41 (35%); mp. 150°C.
Example B20 4-(3-chlorophenyl)-α0-(4-chlorophenyl)-2-hydrazino-α6-(l-methyl-lH-imidazol-5-yl)- 3,6-quinolinedimethanol (0.00371 mol) was added to ΗC1 IN (25 ml) and stirred at room temperature. A solution of NaNO2 (0.00408 mol) in Η2O (5 ml) was added dropwise and the resulting reaction mixture was stirred and refluxed for one hour. The mixture was allowed to cool to room temperature, then poured out into ice-water and the precipitate was filtered off, washed with water, washed with diethyl ether and dried, yielding 1.95 g of compound 82 (92%; mp: > 280 °C).
Example B21
HCl 3N (20ml) was added dropwise to a solution of compound 51 (0.0123 mol) in H2O (80ml) (until pH=2). The mixture was stirred for 1 hour. The precipitate was filtered off and dried, yielding 5g of compound 53 (70%); mp. >260°C.
Example B22
NH2CH3 (2.5ml) was added dropwise at room temperature to a mixture of compound 25 and compound 47 (0.0086 mol) in THF (45ml). The mixture was stirred at 40°C for 30 min, hydrolized and extracted with CH2C12. The organic layer was separated, dried, filtered and the solvent was evaporated. The residue was purified by column chromatography over silica gel (eluent: toluene/2-propanol/Nt-UOH 85/15/1). Three fractions were collected and their solvents were evaporated. Fraction 1 was crystallized from CH3CN and DIPE. The precipitate was filtered off and dried, yielding 0.4g of compound 48 (9%); mp. 167°C. Fraction 2 was crystallized from CH3CN and diethyl ether. The precipitate was filtered off and dried, yielding 0.6g of compound 49 (13%); mp. 206°C.
Example B23
(R)-l-(l-isocyanatoethyl)naphthalene (0.0039 mol) was added to a mixture of compound 18 (0.00196 mol) in THF (10ml). The mixture was stirred and refluxed for 18 hours, hydrolized and extracted with CH C12. The organic layer was separated, dried, filtered and the solvent was evaporated. The residue was purified by column chromatography over silica gel (eluent: cyclohexane/2-propanol/NH4OH 70/30/1). The pure fractions were collected and the solvent was evaporated. The residue was crystallized from CH3CN and DIPE. The precipitate was filtered off and dried, yielding 0.55g of compound 135 (40%). Example B24
Compound 18 (0.008 mol) was purified and separated into its enantiomers by chiral column chromatography over Chiralcel OD (eluent: ethanol 100%). Two pure fractions were collected and their solvents were evaporated. Fraction 1 was converted into the ethanedioic acid salt (1:1). The precipitate was filtered off and dried, yielding 1.59g of compound 28 (34%); mp. 180°C. Fraction 2 was converted into the ethanedioic acid salt (1:1) and crystallized from ethanol. The precipitate was filtered off and dried, yielding 1.85g of compound 27 (39%); mp. 172°C.
Example B25
K2CO3 (0.096 mol) was added at 5°C to a mixture of hydjoxylamine hydrochloride (0.09 mol) in H2O (10ml). The mixture was stirred for 15 min. A solution of compound 69 (0.003 mol) in THF (15ml) was added dropwise. The mixture was stirred at 5°C for 30 min. Ice water was added and the mixture was extracted with CH2CI2. The organic layer was separated, dried, filtered and the solvent was evaporated. The residue was purified by column chromatography over silica gel (eluent: CH2CI2 CH3OH/NH4OH 95/5/0.3). The pure fractions were collected and the
solvent was evaporated. The residue was crystallized from EtOAc. The precipitate was filtered off and dried, yielding 0J7g of compound 98 (11%); mp. 191°C.
Example B26
NFLtOH cone. (10ml) was added dropwise at 5°C to a mixture of compound 76 (0.00464 mol) in THF (20ml). The mixture was stirred at room temperature for 2 hours, poured out on ice and extracted with CH2CI2. The organic layer was separated, dried, filtered and the solvent was evaporated. The residue was purified by column chromatography over silica gel (eluent: CH^ /CHsOH/NHtOH 95/5/0J). Two pure fractions were collected and their solvents were evaporated. Fraction 1 was crystallized from CH3CN and DIPE. The precipitate was filtered off and dried, yielding 0.55g of compound 77 (21%); mp. >250°C. Fraction 2 was purified by column chromatography over silica gel (eluent: CH2Cl2/CH3OH7 NH-tOH 95/5/0.5; 20-45 μm). The pure fractions were collected and the solvent was evaporated. The residue was crystallized from CH3CN. The precipitate was filtered off and dried, yielding 0J7g of compound 80 (6%); mp. >250°C.
Example B27
Methanamine (30ml; 40% in H2O) was added to a mixture of compound 119 (0.004 mol) in THF (20ml). The mixture was stirred for 1 hour. K2CO3 10% was added and the mixture was extracted with CH2CI2. The organic layer was separated, dried, filtered and the solvent was evaporated. The residue was purified by column chromatography over silica gel (eluent: CH2CI2/CH3OH/NH OH 90/10/0.1 and 80/20/0.1). The pure fractions were collected and the solvent was evaporated. The residue was crystallized from THF and diethyl ether. The precipitate was filtered off and dried, yielding l.lg of compound 121 (48%); mp. 224°C. Example B28
LiAlH. (0.00663 mol) was added at 5°C under N2 flow to THF (30ml). Then compound 52 (0.00331 mol) was added portionwise. The mixture was stirred at room temperature for 1 hour. EtOAc was added. The mixture was hydrolized cold, filtered over celite and washed with EtOAc. The filtrate was extracted with EtOAc. The organic layer was separated, washed with H2O, dried, filtered and the solvent was evaporated. The residue was purified by column chromatography over silica gel (eluent: cyclohexane/2-propanol/NHtOH 80/20/1). The pure fractions were collected and the solvent was evaporated. This fraction was crystallized from 2-propanone and diethyl ether. The precipitate was filtered off and dried, yielding 0.98g of compound 75 (51%)).
The following compounds were prepared analogous to the one of the above examples (the example number analogous to which they were prepared is indicated between square brackets after the compound number).
C. Pharmacological example- Example CJ : "In Vitro Assay for Inhibition of Farnesyl Protein Transferase" : An in vitro assay for inhibition of farnesyl transferase was performed essentially as described in WO 98/40383 , pages 33-34.
Example C.2 : "Ras-Transformed Cell Phenotype Reversion Assay".
The rαs-transformed cell phenotype reversion assay was performed essentially as described in WO 98/40383 , pages 34-36.
Example C.3 : "Farnesyl Protein Transferase Inhibitor Secondary Tumor Model". The farnesyl protein transferase inhibitor secondary tumor model was used as described in WO 98/40383 , page 37.
Example CJ : " Geranylgeranyltransferase Type I Assay ".
Background: The enzyme GGTase I catalyzes the covalent attachment of a C-20 geranylgeranyl moiety derived from geranylgeranyl pyrophosphate to the K-ras oncogene product p21^"ra's. The geranylgeranylation proceeds via formation of a thioether linkage to a single, specific cysteine residue contained in a cys-A-A-X motif wherein A represents neutral amino acids and X represents a C-terminal leucine or methionine. Farnesylation of H,N, and K-ras isoforms by farnesyl protein transferase is required for activation and attachment of p21ra5 to plasma membranes. However, the K-ras isoform, which is the dominant isoform of ras in human tumors, is also isoprenylated by GGTase I. Therefore, inhibitors of GGTase I may inhibit the aberrant
growth of K-ras transformed human tumors which are resistant to protein farnesyl transferase inhibitors.
Methods: Compounds were screened in vitro using GGTase I enzyme prepared from
Kirsten virus transformed human osteosarcoma (KHOS) cells. The assay measures the covalent attachment of radioactivity from [-1H]-geranylgeranyl pyrophosphate to the K- ras peptide substrate biotinKKKKKKSKTLCVIM or biotinYRASNRSCAIL substrate.
Measurements: Percent control GGTase I activity.
Derived Variables: Control enzyme activity = [CPM -Η-geranylgeranyl peptide product in the presence of vehicle solvent]
Test compound concentration = 10 μM. Test compound % control activity = (CPM -Η- geranylgeranyl peptide product in the presence of test compound /control enzyme activity) X 100%)
Standard Conditions: Compounds were dissolved in DMSO at a concentration of 20 mM. Further dilutions were prepared in DMSO. The final concentration of DMSO in the assay medium was 10%. The compound concentration tested for screening was 10 μM.
D. Composition example : Film-coated tablets Pr-vP-aratioπ.pf tablet core A mixture of 100 g of a compound of formula (I), 570 g lactose and 200 g starch is mixed well and thereafter humidified with a solution of 5 g sodium dodecyl sulfate and 10 g polyvinyl-pyrrolidone in about 200 ml of water. The wet powder mixture is sieved, dried and sieved again. Then there are added 100 g microcrystalline cellulose and 15 g hydrogenated vegetable oil. The whole is mixed well and compressed into tablets, giving 10.000 tablets, each comprising 10 mg of a compound of formula (I). Coating
To a solution of 10 g methyl cellulose in 75 ml of denaturated ethanol there is added a solution of 5 g of ethyl cellulose in 150 ml of dichloromethane. Then there are added 75 ml of dichloromethane and 2.5 ml 1,2,3-propanetriol. 10 g of polyethylene glycol is molten and dissolved in 75 ml of dichloromethane. The latter solution is added to the former and then there are added 2.5 g of magnesium octadecanoate, 5 g of polyvinyl- pyrrolidone and 30 ml of concentrated colour suspension and the whole is homogenated. The tablet cores are coated with the thus obtained mixture in a coating apparatus.
Claims
1. A compound of formula (I)
=N-CR6=CR7- (x-1), =CR6-CR7=CR8- (x-6),
=N-N=CR6- (x-2), =CR6-N=CR7- (x-7),
=N-NH-C(=O)- (x-3), =CR6-NH-C(=O)- (x-8), or
=N-N=N- (x-4), =CR6-N=N- (x-9);
=N-CR6=N- (x-5), wherein each R6, R7 and R8 are independently hydrogen, C1-4alkyl, hydroxy, C1-4alkyloxy, aryloxy, C1-4alkyloxycarbonyl, hydroxyC1-4alkyl, Cι-4alkyloxyC1- 4alkyl, mono- or di(Cι-4alkyl)aminoCι-4alkyl, cyano, amino, thio, C1-4alkylthio, arylthio or aryl; >γi_γ2_ s a trjvajent rac|icaι 0f formula
>CH-CHR (y-i),
>C=N- (y-2), >CH-NR9- (y-3),or >C=CR > 9y- (y-4); wherein each R9 independently is hydrogen, halo, halocarbonyl, aminocarbonyl, hydroxyCι- alkyl, cyano, carboxyl, C].4alkyl,
C1-4alkyloxyC1-4alkyl, C1-4alkyloxycarbonyl, mono- or di(C1.4alkyl)amino, mono- or d Q. 4alkyl)aminoC1-4alkyl, aryl; r and s are each independently 0, 1, 2, 3, 4 or 5; t is O, 1, 2 or 3; each R1 and R2 are independently hydroxy, halo, cyano, Cι_6alkyl, trihalomethyl, trihalomethoxy, d-ealkenyl, C,-6alkyloxy, hydroxyC1-6alkyloxy, d-6alkylthio, Cι-6alkyloxyC,-6alkyloxy, Ct-6alkyloxycarbonyl, aminoCι-6alkyloxy, mono- or
di(C,-6alkyl)amino, mono- or di(Cι-6alkyl)aminoCι-6alkyloxy, aryl, aryld-6alkyl, aryloxy or arylC1-6alkyloxy, hydroxycarbonyl, CI-6alkyloxycarbonyl, aminocarbonyl, aminod-ealkyl, mono- or di(C1-6alkyl)aminocarbonyl, mono- or dKCi-όalky aminoCi-ealkyl; or two R1 or R2 substituents adjacent to one another on the phenyl ring may independently form together a bivalent radical of formula
-O-CH2-O- (a-1)-
-O-CH2-CH2-O- (a-2),
-O=CH=CH- (a-3), -O-CH2-CH2- (a-4),
-O-CH2-CH2- CH2- (a-5), or
-CH=CH-CH=CH- (a-6);
R3 is hydrogen, halo, d-6alkyl, cyano, halod-6alkyl, hydroxyCι-6alkyl, cyanod-6alkyl, aminoCι-6alkyl, Cι-6alkyloxyC1-6alkyl, Cι.6alkylthioCι-6alkyl, aminocarbonyld-βalkyl, hydroxycarbonyl, hydroxycarbonylCι-6alkyl, d-6alkyloxycarbonylCι-6alkyl, Ci-βalkylcarbonyld-βalkyi, d-6alkyloxycarbonyl, aryl, arylC,-6alkyloxyCι-.6alkyl, mono- or di(d-6alkyl)aminoCi-6alkyl; or a radical of formula
-O-R10 Φ-1)' -S-R10 (b-2).
-NRnR12 (b-3), wherein R10 is hydrogen, Cι-6alkyl, d-6alkylcarbonyl, aryl, arylCι-6alkyl, d-6alkyloxycarbonyld-6alkyl, or a radical of formula -Alk-OR13 or -Alk-NR14R15;
R" is hydrogen, Cι-6alkyl, aryl or aryld-6alkyl; R12 is hydrogen, Cι-6alkyl, aryl, hydroxy, amino, d-6alkyloxy,
Cι-6alkylcarbonyld-6alkyl, arylCι-6alkyl, Ci-6alkylcarbonylamino, mono- or di(Cι-6alkyl)amino, d-6alkylcarbonyl, aminocarbonyl, arylcarbonyl, haloCj-
6alkylcarbonyl, arylCi-ealkylcarbonyl, Cι-6alkyloxycarbonyl,
C,-6alkyloxyCι-6alkylcarbonyl, mono- or di(Cι-6alkyl)aminocarbonyl wherein the alkyl moiety may optionally be substituted by one or more substituents independently selected from aryl or d-3alkyloxycarbonyl, aminocarbonylcarbonyl, mono- or di(C1-6alkyl)aminoC1.6alkylcarbonyl, or a radical or formula -Alk-OR13 or
-Alk-NR14R15; wherein Alk is Cι-6alkanediyl; R13 is hydrogen, Cι-6alkyl, Cι-6alkylcarbonyl, hydroxyCι-6alkyl, aryl or aryld-6alkyl;
R14 is hydrogen, Cι-6alkyl, aryl or arylCι-6alkyl;
R15 is hydrogen, Cι-6alkyl, C,-6alkylcarbonyl, aryl or arylCι-6alkyl;
R4 is a radical of formula
2. A compound according to claim 1 wherein each R1 and R2 are independently hydroxy, halo, cyano, Ci-βalkyl, trihalomethyl, trihalomethoxy, C2-6alkenyl, d-6alkyloxy, hydroxyC,-6alkyloxy, C,-6alkylthio, d-ealkyloxyd-ealkyloxy, C,-6alkyloxycarbonyl, aminod-6alkyloxy, mono- or di(Cι-6alkyl)amino, mono- or d Ci-ealky aminod-ealkyloxy, aryl, aryld-6alkyl, aryloxy or arylC1-6alkyloxy, hydroxycarbonyl, C1-6alkyloxycarbonyl; or
1 two R or R substituents adjacent to one another on the phenyl ring may independently form together a bivalent radical of formula
-O-CH2-O- (a-1),
-O-CH2-CH2-O- (a-2),
-0=CH=CH- (a-3), -O-CH2-CH2- (a-4),
-O-CH2-CH2- CH2- (a-5), or
-CH=CH-CH=CH- (a-6);
R16 is hydrogen, halo, aryl, C,.6alkyl, hydroxyd-6alkyl, Cι-6alkyloxyd-6alkyl, d-6alkyloxy, Cι-6alkylthio, amino, mono- or di(C1- alkyl)amino, hydroxycarbonyl, C,-6alkyloxycarbonyl, Cι-6alkylthiod-6alkyl, C1-6alkylS(O)Cι-6alkyl or C1-6alkylS(O)2C1-6alkyl;
R16 may also be bound to one of the nitrogen atoms in the imidazole ring of formula (c-1), in which case the meaning of R16 when bound to the nitrogen is limited to hydrogen, aryl, Cι-6alkyl, hydroxyC,.6alkyl, C1-6alkyloxyC1-6alkyl, C1-6alkyloxycarbonyl, C,-6alkylS(O)d-6alkyl or d-6alkylS(O)2d-6alkyl;
R17 is hydrogen, d-6alkyl, trifluoromethyl or di(Cι-4alkyl)aminosulfonyl.
3. A compound according to any of claims 1 to 2 wherein =X*-X2-X3 is a trivalent radical of formula (x-1), (x-2), (x-3), (x-4) or (x-9) wherein each R6 independently is hydrogen, C!-4alkyl, C1-4alkyloxycarbonyl, amino or aryl and R7 is hydrogen; >γi_γ2_ ■ s a trivalent radical of formula (y-1), (y-2), (y-3), or (y-4) wherein each R9 independently is hydrogen, halo, carboxyl, C1-4alkyl or C1-4alkyloxycarbonyl; r is 0, 1 or 2; s is 0 or 1; t is 0; R1 is halo, d-6alkyl or two R1 substituents ortho to one another on the phenyl ring may independently form together a bivalent radical of formula (a-1); R2 is halo; R3 is halo or a radical of formula (b-1) or (b-3) wherein R10 is hydrogen or a radical of formula -Alk-OR13, R11 is hydrogen, R12 is hydrogen, Cι-6alkyl, Cι-6alkylcarbonyl, hydroxy, C,-6alkyloxy or mono- or di(C1-6alkyl)aminoC,-6alkylcarbonyl, Alk is Cι-6alkanediyl and R13 is hydrogen; R4 is a radical of formula (c-1) or (c-2) wherein R16 is hydrogen, halo or mono- or di(Cι-4alkyl)amino; R17 is hydrogen or d-6alkyl; aryl is phenyl.
4. A compound according to any of claims 1 to 3 wherein =X1-X2-X3 is a trivalent radical of formula (x-1), >Y!-Y2 is a trivalent radical of formula (y-4), r is 0 or 1, s is 1, t is 0, R is 3-chloro, R is 4-chloro or 4-fluoro, R is hydrogen or a radical of formula (b-1) or (b-3), R4 is a radical of formula (c-1) or (c-2), R6 is hydrogen, R7 is hydrogen, R9 is hydrogen, R10 is hydrogen, Rn is hydrogen and R12 is hydrogen.
5. A compound according to any one of claims 1 to 4 wherein =X1-X2-X3 is a trivalent radical of formula (x-2) or (x-3), >Y'-Y2 is a trivalent radical of formula (y-2), (y-3) or (y-4), r and s are 1, t is 0, R1 is 3-chloro or 3-methyl, R2 is 4-chloro, R3 is a radical of formula (b-1) or (b-3), R4 is a radical of formula (c-2), R6 is - 4alkyl, R is hydrogen, R10 and R11 are hydrogen and R12 is hydrogen or hydroxy.
6. A compound according to claim 1 or 2 selected from :
7-[(4-fluorophenyl)(lH-imidazol-l-yl)methyl]-5-phenylimidazo[l,2-a]quinoline; α-(4-chlorophenyl)-α-(l-methyl-lH-imidazol-5-yl)-5-phenylimidazo[l,2- a]quinoline-7 -methanol; 5-(3-chlorophenyl)-α-(4-chlorophenyl)-α-(l -methyl- 1H- imidazol-5-yl)-imidazo[l,2-a]quinoline-7-methanol; 5-(3-chlorophenyl)-α-(4- chlorophenyl)-α-(l-methyl-lH-imidazol-5-yl)imidazo[l,2-a]quinoline-7- methanamine; 5-(3-chlorophenyl)-α-(4-chlorophenyl)-α-(l-methyl-lH- imidazol-5-yl)tetrazolo[ 1 ,5-a]quinoline-7-methanamine; 5-(3-chlorophenyl)-α-(4- chlorophenyl)-l-methyl-α-(l-methyl-lH-imidazol-5-yl)-l,2,4-triazolo[4,3- a]quinoline-7 -methanol; 5-(3-chlorophenyl)-α-(4-chlorophenyl)-α-(l-methyl-lH- imidazol-5-yl)tetrazolo[ 1 ,5-a]quinoline-7-methanamine; 5-(3-chlorophenyl)-α-(4- chlorophenyl)-α-(l-methyl-lH-imidazol-5-yl)teμ-azolo[l,5-a]quinazoline-7- methanol; 5-(3-chlorophenyl)- -(4-chlorophenyl)-4,5-dihydro-α-(l -methyl- 1H- imidazol-5-yl)tetrazolo[l,5-a]quinazoline-7 -methanol; 5-(3-chlorophenyl)-α-(4- chlorophenyl)- -( 1 -methyl- lH-imidazol-5-yl)tetrazolo[ 1 ,5-a]quinazoline-7- methanamine; 5-(3-chlorophenyl)-α-(4-chlorophenyl)-N-hydroxy-α-(l-methyl-lH- imidazol-5-yl)tetrahydro[ 1 ,5-a]quinoline-7-methanamine; α-(4-chlorophenyl)-α- (l-methyl-lH-imidazol-5-yl)-5-(3-methylphenyl)tetrazolo[l,5-a]quinoline-7- methanamine; pharmaceutically acceptable acid addition salt or a stereochemically isomeric form thereof.
7. A pharmaceutical composition comprising a pharmaceutically acceptable carrier, and as active ingredient a therapeutically effective amount of a compound as described in any one of claims 1 to 6.
8. A process for preparing a pharmaceutical composition as claimed in claim 7 wherein a therapeutically effective amount of a compound as claimed in any one of claims 1 to 6 is intimately mixed with a pharmaceutically acceptable carrier.
9. A compound of formula (II)
10. A compound according to any one of claims 1 to 6 for use as a medicine.
11. A process for preparing a compound as claimed in claim 1, wherein a) =X'-X2-X3 is a trivalent radical of formula (x-1) and R6 and R7 are hydrogen, represented by compounds of formula (I-l), by reacting an intermediate of formula (II) with a reagent of formula (III) or a functional derivative thereof, wherein W1 is a leaving group, followed by an intramolecular cyclization;
1.) or, compounds of formula (I) are converted into each other following art-known transformation reactions; or if desired; a compound of formula (I) is converted into a pharmaceutically acceptable acid addition salt, or conversely, an acid addition salt of a compound of formula (I) is converted into a free base form with alkali; and, if desired, preparing stereochemically isomeric forms thereof.
12. A process for preparing an intermediate of formula (II) as claimed in claim 9 wherein an intermediate of formula (XV) is reacted with a halogenating reagent;
Priority Applications (21)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| HR20010454A HRP20010454B1 (en) | 1998-12-23 | 1999-12-17 | 1,2-annelated quinoline derivatives |
| UA2001064401A UA71592C2 (en) | 1998-12-23 | 1999-12-17 | Annelated 1,2-quinoline derivatives, a method for the preparation thereof (variants), a pharmaceutical composition containing them, an intermediary compound and a method for the preparation thereof |
| AT99969220T ATE240327T1 (en) | 1998-12-23 | 1999-12-17 | 1,2-ANNELATED QUINOLINE DERIVATIVES |
| HK02100160.2A HK1038746B (en) | 1998-12-23 | 1999-12-17 | 1,2-annelated quinoline derivatives |
| HU0104582A HU229404B1 (en) | 1998-12-23 | 1999-12-17 | 1,2-annelated quinoline derivatives |
| IL14385999A IL143859A0 (en) | 1998-12-23 | 1999-12-17 | 1,2-annelated quinoline derivatives |
| US09/868,992 US6458800B1 (en) | 1998-12-23 | 1999-12-17 | 1,2-annelated quinoline derivatives |
| EA200100708A EA004542B1 (en) | 1998-12-23 | 1999-12-17 | 1,2-annelated quinoline derivatives |
| BR9916827-8A BR9916827A (en) | 1998-12-23 | 1999-12-17 | 1,2-ringed quinoline derivatives |
| DE69907964T DE69907964T2 (en) | 1998-12-23 | 1999-12-17 | 1,2-FELLENED CHINOLINE DERIVATIVES |
| PL349504A PL199080B1 (en) | 1998-12-23 | 1999-12-17 | 1,2-annelated quinoline derivatives and method of obtaining same |
| DK99969220T DK1140935T3 (en) | 1998-12-23 | 1999-12-17 | 1,2-celled quinoline derivatives |
| SK873-2001A SK286072B6 (en) | 1998-12-23 | 1999-12-17 | 1,2-Annelated quinoline derivatives, method for their preparation, intermediates, pharmaceutical composition and their use |
| EEP200100318A EE04962B1 (en) | 1998-12-23 | 1999-12-17 | The quinoline compound, the pharmaceutical composition containing it, the use of the compound as a medicament, and the process for the preparation of the compound and the composition |
| AU27953/00A AU765437B2 (en) | 1998-12-23 | 1999-12-17 | 1,2-annelated quinoline derivatives |
| SI9930350T SI1140935T1 (en) | 1998-12-23 | 1999-12-17 | 1,2-annelated quinoline derivatives |
| JP2000590995A JP4725940B2 (en) | 1998-12-23 | 1999-12-17 | 1,2-Cyclic quinoline derivatives |
| EP99969220A EP1140935B1 (en) | 1998-12-23 | 1999-12-17 | 1,2-annelated quinoline derivatives |
| CA2355717A CA2355717C (en) | 1998-12-23 | 1999-12-17 | 1,2-annelated quinoline derivatives |
| IL143859A IL143859A (en) | 1998-12-23 | 2001-06-20 | 7-(??-imidazolyl benzyl)-5-phenyl-1,2-annelated quinoline derivatives, pharmaceutical compositions containing them, the corresponding substituted quinoline intermediates thereof and their preparation |
| NO20013088A NO318922B1 (en) | 1998-12-23 | 2001-06-21 | 1,2-annealed quinoline derivatives |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP98204444.8 | 1998-12-23 | ||
| EP98204444 | 1998-12-23 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| WO2000039082A2 true WO2000039082A2 (en) | 2000-07-06 |
| WO2000039082A3 WO2000039082A3 (en) | 2000-10-26 |
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ID=8234557
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PCT/EP1999/010214 Ceased WO2000039082A2 (en) | 1998-12-23 | 1999-12-17 | 1,2-annelated quinoline derivatives |
Country Status (32)
| Country | Link |
|---|---|
| US (2) | US6458800B1 (en) |
| EP (1) | EP1140935B1 (en) |
| JP (1) | JP4725940B2 (en) |
| KR (2) | KR100712226B1 (en) |
| CN (1) | CN1178938C (en) |
| AR (1) | AR021995A1 (en) |
| AT (1) | ATE240327T1 (en) |
| AU (1) | AU765437B2 (en) |
| BG (1) | BG65124B1 (en) |
| BR (1) | BR9916827A (en) |
| CA (1) | CA2355717C (en) |
| CZ (1) | CZ302374B6 (en) |
| DE (1) | DE69907964T2 (en) |
| DK (1) | DK1140935T3 (en) |
| EA (1) | EA004542B1 (en) |
| EE (1) | EE04962B1 (en) |
| ES (1) | ES2200591T3 (en) |
| HK (1) | HK1038746B (en) |
| HR (1) | HRP20010454B1 (en) |
| HU (1) | HU229404B1 (en) |
| ID (1) | ID29241A (en) |
| IL (2) | IL143859A0 (en) |
| NO (1) | NO318922B1 (en) |
| PL (1) | PL199080B1 (en) |
| PT (1) | PT1140935E (en) |
| SI (1) | SI1140935T1 (en) |
| SK (1) | SK286072B6 (en) |
| TR (1) | TR200101961T2 (en) |
| TW (1) | TW531533B (en) |
| UA (1) | UA71592C2 (en) |
| WO (1) | WO2000039082A2 (en) |
| ZA (1) | ZA200105136B (en) |
Cited By (54)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
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Families Citing this family (13)
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Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA2002864C (en) | 1988-11-29 | 1999-11-16 | Eddy J. E. Freyne | (1h-azol-1-ylmethyl) substituted quinoline, quinazoline or quinoxaline derivatives |
| TW349948B (en) * | 1995-10-31 | 1999-01-11 | Janssen Pharmaceutica Nv | Farnesyl transferase inhibiting 2-quinolone derivatives |
| SK283335B6 (en) * | 1995-12-08 | 2003-06-03 | Janssen Pharmaceutica N. V. | (Imidazol-5-yl)methyl-2-quinolinone derivatives, method and intermediates for their production, their use and pharmaceutical compositions based on them |
| TW591030B (en) * | 1997-03-10 | 2004-06-11 | Janssen Pharmaceutica Nv | Farnesyl transferase inhibiting 1,8-annelated quinolinone derivatives substituted with N- or C-linked imidazoles |
| RU2205831C2 (en) * | 1997-04-25 | 2003-06-10 | Янссен Фармацевтика Н.В. | Quinazolinones inhibiting farnesyltransferase activity |
| AU740603B2 (en) * | 1997-06-02 | 2001-11-08 | Janssen Pharmaceutica N.V. | (imidazol-5-yl)methyl-2-quinolinone derivatives as inhibitors of smooth muscle cell proliferation |
-
1999
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| US8697716B2 (en) | 2006-04-20 | 2014-04-15 | Janssen Pharmaceutica Nv | Method of inhibiting C-KIT kinase |
| US9266866B2 (en) | 2006-04-20 | 2016-02-23 | Janssen Pharmaceutica Nv | Inhibitors of C-FMS kinase |
| US8481564B2 (en) | 2006-04-20 | 2013-07-09 | Janssen Pharmaceutica, N.V. | Inhibitors of c-fms kinase |
| US8759347B2 (en) | 2006-04-20 | 2014-06-24 | Janssen Pharmaceutica Nv | Inhibitors of C-FMS kinase |
| US8859602B2 (en) | 2006-04-20 | 2014-10-14 | Janssen Pharmaceutica Nv | Inhibitors of c-fms kinase |
| US8895584B2 (en) | 2006-04-20 | 2014-11-25 | Janssen Pharmaceutica Nv | Inhibitors of c-fms kinase |
| US8933091B2 (en) | 2006-04-20 | 2015-01-13 | Janssen Pharmaceutica Nv | Method of inhibiting C-KIT kinase |
| US9296726B2 (en) | 2006-04-20 | 2016-03-29 | Janssen Pharmaceutica Nv | Inhibitors of c-fms kinase |
| US9394289B2 (en) | 2006-04-20 | 2016-07-19 | Janssen Pharmaceutica Nv | Inhibitors of c-fms kinase |
| US9526731B2 (en) | 2006-04-20 | 2016-12-27 | Janssen Pharmaceutica Nv | Method of inhibiting C-KIT kinase |
| US9403804B2 (en) | 2006-04-20 | 2016-08-02 | Janssen Pharmaceutica Nv | Inhibitors of c-fms kinase |
| US8497376B2 (en) | 2007-10-17 | 2013-07-30 | Janssen Pharmaceutica N.V. | Inhibitors of c-fms kinase |
| US9145354B2 (en) | 2011-11-01 | 2015-09-29 | Astex Therapeutics Limited | Pharmaceutical compounds |
| US9029352B2 (en) | 2012-08-07 | 2015-05-12 | Janssen Pharmaceutica Nv | Process for the preparation of C-FMS kinase inhibitors |
| US9303046B2 (en) | 2012-08-07 | 2016-04-05 | Janssen Pharmaceutica Nv | Process for the preparation of heterocyclic ester derivatives |
| US9309222B2 (en) | 2012-10-16 | 2016-04-12 | Janssen Pharmaceutica Nv | Phenyl linked quinolinyl modulators of RORγt |
| US9290476B2 (en) | 2012-10-16 | 2016-03-22 | Janssen Pharmaceutica Nv | Methylene linked quinolinyl modulators of RORγt |
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| US9284308B2 (en) | 2013-10-15 | 2016-03-15 | Janssen Pharmaceutica Nv | Methylene linked quinolinyl modulators of RORγt |
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| US9403816B2 (en) | 2013-10-15 | 2016-08-02 | Janssen Pharmaceutica Nv | Phenyl linked quinolinyl modulators of RORγt |
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| US9624225B2 (en) | 2013-10-15 | 2017-04-18 | Janssen Pharmaceutica Nv | Quinolinyl modulators of RORγt |
| US10369146B2 (en) | 2013-10-15 | 2019-08-06 | Janssen Pharmaceutica Nv | Phenyl linked quinolinyl modulators of RORγt |
| US9346782B2 (en) | 2013-10-15 | 2016-05-24 | Janssen Pharmaceutica Nv | Alkyl linked quinolinyl modulators of RORγt |
| US10201546B2 (en) | 2013-10-15 | 2019-02-12 | Janssen Pharmaceutica Nv | Quinolinyl modulators of RORγt |
| US11793793B2 (en) | 2014-05-01 | 2023-10-24 | Eiger Biopharmaceuticals, Inc. | Treatment of hepatitis delta virus infection |
| US12290509B2 (en) | 2014-05-01 | 2025-05-06 | Eit Pharma, Inc. | Treatment of hepatitis delta virus infection |
| US11311519B2 (en) | 2014-05-01 | 2022-04-26 | Eiger Biopharmaceuticals, Inc. | Treatment of hepatitis delta virus infection |
| US10828283B2 (en) | 2014-05-01 | 2020-11-10 | Eiger Biopharmaceuticals, Inc. | Treatment of hepatitis delta virus infection |
| US12029819B2 (en) | 2015-04-21 | 2024-07-09 | Eiger Biopharmaceuticals, Inc. | Pharmaceutical compositions comprising lonafarnib and ritonavir |
| US11517532B2 (en) | 2015-04-21 | 2022-12-06 | Eiger Biopharmaceuticals, Inc. | Methods of treating hepatitis delta virus infection |
| US10835496B2 (en) | 2015-04-21 | 2020-11-17 | Eiger Biopharmaceuticals, Inc. | Pharmaceutical compositions comprising lonafarnib and ritonavir |
| US10335404B2 (en) | 2015-08-17 | 2019-07-02 | Kura Oncology, Inc. | Methods of treating cancer patients with farnesyltransferase inhibitors |
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| US10022364B2 (en) | 2015-08-17 | 2018-07-17 | Kura Oncology, Inc. | Methods of treating cancer patients with farnesyltransferase inhibitors |
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| US11124839B2 (en) | 2016-11-03 | 2021-09-21 | Kura Oncology, Inc. | Methods of treating cancer patients with farnesyltransferase inhibitors |
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