NO851029L - ANALOGY PROCEDURE FOR THE PREPARATION OF THERAPEUTICALLY ACTIVE ISOCHROMAN AND OCSEPIN DERIVATIVES - Google Patents
ANALOGY PROCEDURE FOR THE PREPARATION OF THERAPEUTICALLY ACTIVE ISOCHROMAN AND OCSEPIN DERIVATIVESInfo
- Publication number
- NO851029L NO851029L NO851029A NO851029A NO851029L NO 851029 L NO851029 L NO 851029L NO 851029 A NO851029 A NO 851029A NO 851029 A NO851029 A NO 851029A NO 851029 L NO851029 L NO 851029L
- Authority
- NO
- Norway
- Prior art keywords
- group
- atoms
- hydrogen atom
- atom
- chlorine
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D311/00—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings
- C07D311/02—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings ortho- or peri-condensed with carbocyclic rings or ring systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/12—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/12—Drugs for disorders of the metabolism for electrolyte homeostasis
- A61P3/14—Drugs for disorders of the metabolism for electrolyte homeostasis for calcium homeostasis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/08—Vasodilators for multiple indications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/12—Antihypertensives
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D311/00—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings
- C07D311/02—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings ortho- or peri-condensed with carbocyclic rings or ring systems
- C07D311/76—Benzo[c]pyrans
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D313/00—Heterocyclic compounds containing rings of more than six members having one oxygen atom as the only ring hetero atom
- C07D313/02—Seven-membered rings
- C07D313/06—Seven-membered rings condensed with carbocyclic rings or ring systems
- C07D313/08—Seven-membered rings condensed with carbocyclic rings or ring systems condensed with one six-membered ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D407/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00
- C07D407/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00 containing two hetero rings
- C07D407/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Veterinary Medicine (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Obesity (AREA)
- Hematology (AREA)
- Diabetes (AREA)
- Urology & Nephrology (AREA)
- Vascular Medicine (AREA)
- Endocrinology (AREA)
- Rheumatology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Pyrane Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Plural Heterocyclic Compounds (AREA)
Description
Denne oppfinnelse angår en fremgangsmåte for fremstillingThis invention relates to a method for manufacturing
av nye substituerte isokromaner og oksepiner med den generelle formel (I) of new substituted isochromanes and oxepines of the general formula (I)
og syreaddisjonssalter derav med verdifulle terapeutiske egenskaper . and acid addition salts thereof with valuable therapeutic properties.
I formel (I) betyrIn formula (I) means
R"<*>" et hydrogenatom eller en lineær eller forgrenet alkylgruppeR"<*>" a hydrogen atom or a linear or branched alkyl group
med opp til 4 C-atomer,with up to 4 C atoms,
R 2 et hydrogenatom eller en lineær eller forgrenet alkylgruppeR 2 a hydrogen atom or a linear or branched alkyl group
med opp til 4 C-atomer, eller sammen med R en alkylen-with up to 4 C atoms, or together with R an alkylene
gruppe med 3 til 5 C-atomer,group with 3 to 5 C atoms,
R 3 et hydrogenatom eller en lineær eller forgrenet alkylgruppeR 3 a hydrogen atom or a linear or branched alkyl group
med opp til 4 C-atomer,with up to 4 C atoms,
R 4 et hydrogenatom eller en lineær eller forgrenet alkylgruppeR 4 a hydrogen atom or a linear or branched alkyl group
med opp til 4 C-atomer,with up to 4 C atoms,
R^ et hydrogenatom eller en lineær eller forgrenet alkylgruppeR^ a hydrogen atom or a linear or branched alkyl group
med 1 til 6 C-atomer eller en pyridinylgruppe,with 1 to 6 C atoms or a pyridinyl group,
R et hydrogenatom, et fluor-, klor- eller bromatom, en lineær eller forgrenet alkylgruppe med 1 til 6 C-atomer, en hydroksy- eller alkoksygruppe med 1 til 4 C-atomer eller en R a hydrogen atom, a fluorine, chlorine or bromine atom, a linear or branched alkyl group with 1 to 6 C atoms, a hydroxy or alkoxy group with 1 to 4 C atoms or a
trifluormetylgruppe,trifluoromethyl group,
R 7 et hydrogenatom, et fluor-, klor- eller bromatom, en lineær eller forgrenet alkylgruppe med 1 til 6 C-atomer, en hydroksy- eller alkoksygruppe med 1 til 4 C-atomer eller R 7 a hydrogen atom, a fluorine, chlorine or bromine atom, a linear or branched alkyl group with 1 to 6 C atoms, a hydroxy or alkoxy group with 1 to 4 C atoms or
sammen med R en metylendioksygruppe,together with R a methylenedioxy group,
R get hydrogenatom, et fluor-, klor- eller bromatom, en hydroksy-eller alkoksygruppe med 1 til 4 C-atomer, R is a hydrogen atom, a fluorine, chlorine or bromine atom, a hydroxy or alkoxy group with 1 to 4 C atoms,
m tallene 1 eller 2, ogm the numbers 1 or 2, and
n tallene 1, 2 eller 3.n the numbers 1, 2 or 3.
Det foretrekkes isokromaner og oksepiner med den generelle formel (Ia) Isochromanes and oxepines of the general formula (Ia) are preferred
12 3 12 3
hvor R , R og R som er like eller forskjellige, betyr et hydrogenatom eller en metylgruppe, where R , R , and R , which are the same or different, mean a hydrogen atom or a methyl group,
5 5
R betyr en isopropyl- eller pyridinylgruppe,R means an isopropyl or pyridinyl group,
R betyr et hydrogen-, fluor- eller kloratom, en trifluormetyl- eller metoksygruppe, R means a hydrogen, fluorine or chlorine atom, a trifluoromethyl or methoxy group,
R 7 betyr et hydrogen-, fluor- eller kloratom, en tertiær butylgruppe, en metoksygruppe eller sammen med R^ en R 7 means a hydrogen, fluorine or chlorine atom, a tertiary butyl group, a methoxy group or together with R^ a
metylendioksygruppe,methylenedioxy group,
R gbetyr et hydrogenatom eller en metoksygruppe,R g represents a hydrogen atom or a methoxy group,
m betyr tallene 1 eller 2, ogm means the numbers 1 or 2, and
n betyr tallene 1 eller 2, og syreaddisjonssalter derav. n means the numbers 1 or 2, and acid addition salts thereof.
Særlig foretrekkes forbindelser med den generelle formel Compounds of the general formula are particularly preferred
(Ib) (Ib)
hvor where
R betyr et hydrogen- eller kloratom eller en metoksygruppe, R "7 betyr et fluor- eller kloratom eller en metoksygruppe, og R g betyr et hydrogenatom eller en metoksygruppe, R means a hydrogen or chlorine atom or a methoxy group, R "7 means a fluorine or chlorine atom or a methoxy group, and R g means a hydrogen atom or a methoxy group,
og syreaddisjonssalter derav.and acid addition salts thereof.
I henhold til oppfinnelsen fremstilles de nye forbindelser ved at et isokroman- eller oksepin-derivat med den generelle formel (II) According to the invention, the new compounds are prepared by an isochroman or oxepine derivative with the general formula (II)
hvor where
12 3 12 3
R , R , R , m og n er som ovenfor angitt, og X betyr et klor-, brom- eller jodatom eller en alkylsulfonyloksy- eller arylsulfonyloksygruppe, omsettes med et fenyl-aminopropyl-acetonitril med den generelle formel (III) R , R , R , m and n are as indicated above, and X means a chlorine, bromine or iodine atom or an alkylsulfonyloxy or arylsulfonyloxy group, is reacted with a phenyl-aminopropyl-acetonitrile of the general formula (III)
hvor where
R<4>, R^, R<6>, R^ og R^ har den ovenfor angitte betydning, og eventuelt overføres den oppnådde forbindelse til et syreaddisjons-salt. R<4>, R^, R<6>, R^ and R^ have the meaning indicated above, and optionally the compound obtained is transferred to an acid addition salt.
Omsetningen utføres fortrinnsvis i et aprotisk oppløsnings-middel, for eksempel toluen, eller i et aprotisk, polart opp-løsningsmiddel, for eksempel dimetylformamid, under tilsetning av et syrebindende middel, for eksempel en uorganisk base såsom natriumkarbonat eller natronlut, eller en organisk base såsom trietylamin. Reaksjonstemperaturen kan velges fra romtempera-tur til 16 0°C. Fortrinnsvis foretas omsetningen mellom 60 og 120°C. The reaction is preferably carried out in an aprotic solvent, for example toluene, or in an aprotic, polar solvent, for example dimethylformamide, with the addition of an acid-binding agent, for example an inorganic base such as sodium carbonate or caustic soda, or an organic base such as triethylamine. The reaction temperature can be selected from room temperature to 16 0°C. The turnover is preferably carried out between 60 and 120°C.
Isokromanene og oksepinene med de generelle formler I, IaThe isochromans and oxpins with the general formulas I, Ia
og Ib inneholder et asymmetrisk karbonatom og kan på kjent måte separeres i sine antipoder. Antipodene oppnår man også når man går ut fra optisk aktive utgangsstoffer. and Ib contain an asymmetric carbon atom and can be separated into their antipodes in a known manner. The antipodes are also obtained when starting from optically active starting materials.
De nye isokromaner og oksepiner med den generelle formel I The new isochromanes and oxepines of the general formula I
kan på vanlig måte overføres til sine syreaddisjonssalter.can be transferred in the usual way to their acid addition salts.
Syrer som er egnet for saltdannelse, er for eksempel saltsyre, bromhydrogensyre, jodhydrogensyre, flussyre, svovelsyre, fosfor-syre, salpetersyre, eddiksyre, propionsyre, smørsyre, kapron-syre, valeriansyre, oksalsyre, malonsyre, ravsyre, maleinsyre, fumarsyre, melkesyre, vinsyre, sitronsyre, eplesyre, benzoe-syre, p-hydroksybenzoesyre, p-aminobenzoesyre, ftalsyre, kanelsyre, salicylsyre, askorbinsyre, metansulfonsyre, etan-fosfonsyre. Acids which are suitable for salt formation are, for example, hydrochloric acid, hydrobromic acid, hydroiodic acid, hydrofluoric acid, sulfuric acid, phosphoric acid, nitric acid, acetic acid, propionic acid, butyric acid, caproic acid, valerian acid, oxalic acid, malonic acid, succinic acid, maleic acid, fumaric acid, lactic acid, tartaric acid, citric acid, malic acid, benzoic acid, p-hydroxybenzoic acid, p-aminobenzoic acid, phthalic acid, cinnamic acid, salicylic acid, ascorbic acid, methanesulfonic acid, ethane-phosphonic acid.
Forbindelsene med den generelle formel I har i isolerte organer og ved dyreforsøk vist verdifulle terapeutiske, særlig kalsiumantagonistiske egenskaper, som ytrer seg ved en blodtrykk-senkning, bradykardi, negativ inotropi og utvidelse av coronare og perifere kar. The compounds of the general formula I have, in isolated organs and in animal experiments, shown valuable therapeutic, particularly calcium-antagonistic properties, which are manifested by a lowering of blood pressure, bradycardia, negative inotropy and dilation of coronary and peripheral vessels.
De nye forbindelser kan således for eksempel anvendes for behandling eller forebyggelse av coronare hjertelidelser og høyt blodtrykk. The new compounds can thus, for example, be used for the treatment or prevention of coronary heart disease and high blood pressure.
De forbindelser med den generelle formel I kan anvendesThe compounds of the general formula I can be used
alene eller i kombinasjon med andre virkestoffer. Egnede an-vendelsesformer er for eksempel tabletter, kapsler, stikkpiller, oppløsninger, safter, emulsjoner eller dispergerbare pulvere. Passende tabletter kan for eksempel fremstilles ved å blande virkestoffet eller virkestoffene med kjente hjelpestoffer, for eksempel inerte fortynningsmidler såsom kalsiumkarbonat, kalsiumfosfat eller melkesukker; sprengmidler såsom mais-stivelse, alginsyre; bindemidler såsom stivelse eller gelatin; smøremidler såsom magnesiumstearat eller talkum og/eller midler som medfører en depotvirkning såsom karboksypolymetylen, karboksymetylcellulose, celluloseacetatftalat eller polyvinyl-acetat. alone or in combination with other active substances. Suitable forms of use are, for example, tablets, capsules, suppositories, solutions, juices, emulsions or dispersible powders. Suitable tablets can, for example, be prepared by mixing the active substance or substances with known excipients, for example inert diluents such as calcium carbonate, calcium phosphate or milk sugar; explosives such as corn starch, alginic acid; binders such as starch or gelatin; lubricants such as magnesium stearate or talc and/or agents which cause a depot effect such as carboxypolymethylene, carboxymethyl cellulose, cellulose acetate phthalate or polyvinyl acetate.
De nye forbindelser med den generelle formel I kan anvendes enteralt eller parenteralt. Ved oral administrering har det vist seg hensiktsmessig med enkeltdoseringer på 5 til 20 mg, fortrinnsvis 10 til 15 mg. The new compounds of the general formula I can be used enterally or parenterally. For oral administration, single doses of 5 to 20 mg, preferably 10 to 15 mg, have proven appropriate.
I den følgende tabell I er de nye forbindelser med den generelle formel I sammenstilt med sine fysikalske karakteristiske data. In the following Table I, the new compounds of the general formula I are compared with their physical characteristic data.
Elueringsmiddelblandinger: Eluent mixtures:
a) CH2C12/CH30H 9:1; b) CH2C12/CH30H 95:5;c)CH2C12/C<H>30H 8:2; d). CH2C<1>2/<C>H3CN/C2H50H 7:2:1 a) CH2Cl2/CH3OH 9:1; b) CH 2 Cl 2 /CH 3 OH 95:5; c) CH 2 Cl 2 /C<H>3 OH 8:2; d). CH2C<1>2/<C>H3CN/C2H5OH 7:2:1
FremstillingseksemplerManufacturing examples
Eksempel 1 Example 1
6,7-dimetoksy-l-{1-[N-(4-cyano-5-metyl-4-(m^trifluormetyl-fenyl)-heksyl)-N-metyl-amino]^metyl}-isokroman 6,7-dimethoxy-1-{1-[N-(4-cyano-5-methyl-4-(m^trifluoromethyl-phenyl)-hexyl)-N-methyl-amino]^methyl}-isochromane
(Tabell 1, forbindelse nr. 31(Table 1, compound no. 31
2 g l-brommetyl-6,7-dimetoksy-isokroman og 2,1 g 2-isopropyl-21 -[3(N-metylaminol-propyl]-2"-(3-trifluormetylfenyl)-acetonitril oppløses i 30 ml absolutt dimetylformamid og omsettes i 15 timer ved 110°C efter tilsetning av 15 ml trietylamin. Efter avdestillering av oppløsningsmidlet utrøres residuet med 50 ml 2N saltsyre og utristes derefter fraksjonert med dietyleter ved stigende pH-verdi. Eterfraksjonene med pH 6 til pH 7,5 samles. Efter tørking med natriumsulfat fjernes oppløsningsmidlet, og råproduktet separeres over silikagel (Lichroprep Si 60, kornstørrelse 15 til 25 ym; Merck) med en middeltrykk-kromatografikolonne ifølge Helmchen (G. Helmchen et al.; Angew. Chem. 91, 64 (1979)) ved 3 til 5 bar. 2 g of 1-bromomethyl-6,7-dimethoxy-isochromane and 2.1 g of 2-isopropyl-21-[3(N-methylaminol-propyl]-2"-(3-trifluoromethylphenyl)-acetonitrile are dissolved in 30 ml of absolute dimethylformamide and reacted for 15 hours at 110°C after the addition of 15 ml of triethylamine. After distilling off the solvent, the residue is stirred with 50 ml of 2N hydrochloric acid and then fractionally extracted with diethyl ether at increasing pH values. The ether fractions with pH 6 to pH 7.5 are collected. After drying with sodium sulfate, the solvent is removed, and the crude product is separated over silica gel (Lichroprep Si 60, grain size 15 to 25 ym; Merck) with a medium pressure chromatography column according to Helmchen (G. Helmchen et al.; Angew. Chem. 91, 64 (1979) ) at 3 to 5 bar.
Man får 0,7 g av forbindelsen som en farveløs, viskøs olje. 0.7 g of the compound is obtained as a colorless, viscous oil.
Rf-verdi: 0,55; Elueringsmiddel: CH2C12/CH30H = 9:1 Rf value: 0.55; Eluent: CH2C12/CH3OH = 9:1
Eksempel 2 Example 2
7,8-dimetoksy-l-{1-[N-(4-cyano-4-(2-fluor-3,4-dimetoksyfenyl)-5-metylheksyl)-N-metylamino]-metyl}-l,3,4,5-tetrahydro-2-benzoksepin (Tabell 1, forbindelse nr. 6) 7,8-dimethoxy-1-{1-[N-(4-cyano-4-(2-fluoro-3,4-dimethoxyphenyl)-5-methylhexyl)-N-methylamino]-methyl}-1,3, 4,5-tetrahydro-2-benzoxepine (Table 1, compound no. 6)
2,1 g l-brommetyl-7,8-dimetoksy-l,3,4,5-tetrahydro-2-benzoksepin og 2,2 g 2-(3,4-dimetoksy-2-fluor-fenyl)-2<1->isopropyl-2"-[3-(N-metylamino)-propyl]-acetonitril oppløses i 30 ml absolutt dimetylformamid. Derefter tilsettes 3 g kaliumkarbonat, og det hele omrøres i 15 timer ved 110°C. Efter den i eksempel 1 beskrevne opparbeidelse foretaes kromatografisk separering. 2.1 g of 1-bromomethyl-7,8-dimethoxy-1,3,4,5-tetrahydro-2-benzoxepine and 2.2 g of 2-(3,4-dimethoxy-2-fluoro-phenyl)-2< 1->isopropyl-2"-[3-(N-methylamino)-propyl]-acetonitrile is dissolved in 30 ml of absolute dimethylformamide. Then 3 g of potassium carbonate are added, and the whole is stirred for 15 hours at 110°C. Following that in example 1 described preparation, chromatographic separation is carried out.
Man får 0,2 g av forbindelsen som en gulaktig, høyviskøs ol je. 0.2 g of the compound is obtained as a yellowish, highly viscous oil.
Eksempel 3 Example 3
6,7-dimetoksy-4,4<1->dimetyl-l-{2-[N-(4-cyano-4-(3-trifluormetyl-fenyl)-5-metylheksyl)-N-metylaminb]-etyl}-isokroman 6,7-dimethoxy-4,4<1->dimethyl-1-{2-[N-(4-cyano-4-(3-trifluoromethyl-phenyl)-5-methylhexyl)-N-methylamineb]-ethyl} -isochromic
(Tabell 1, forbindelse nr. 8)(Table 1, compound no. 8)
2 g 2-brometyl-6,7-dimetoksy-4,4<1->dimetylisokroman og2 g of 2-bromomethyl-6,7-dimethoxy-4,4<1->dimethylisochromane and
2,1 g 2-isopropyl-2 ' - [3- (N-metylamino) -propyl] -2"-.(3-trif luor-metylf enyl)-acetonitril oppløses i 30 ml absolutt dimetylformamid. Derefter tilsettes 3 g kaliumkarbonat, hvor det hele omrøres i 15 timer ved 110°C. Efter den i eksempel 1 beskrevne opparbeidelse foretas kromatografisk separering. 2.1 g of 2-isopropyl-2'-[3-(N-methylamino)-propyl]-2"-(3-trifluoromethylphenyl)-acetonitrile are dissolved in 30 ml of absolute dimethylformamide. Then 3 g of potassium carbonate are added , where the whole is stirred for 15 hours at 110° C. After the preparation described in example 1, chromatographic separation is carried out.
Man oppnår 1,15 g av forbindelsen som en farveløs, høy-viskøs olje. 1.15 g of the compound is obtained as a colorless, highly viscous oil.
Eksempel 4 6,7-dimetoksy-l-{2-[N-(4-cyano-4-(4-fluorfenyl)-5-metylheksyl)-N-metylamino]-etyl}-l-metyl-isokroman (Tabell 1, forbindelse nr. 10) 8 g 6,7 dimetoksy-l-metyl-1-[2-(p-tosyloksy)etyl-isokroman og 5 g 2-(4-fluorfenyl)-2'-isopropy1-2"-[3-(N-metylamino)-propyl]-acetonitril oppløses i 50 ml toluen og omrøres i 15 timer ved 115°C efter tilsetning av 3 ml trietylamin og 3 g kaliumkarbonat. Efter inndampningen opptaes residuet i 100 ml vann og ekstraheres med 100 ml dietyleter. Efter fraskillelse av vannfasen settes 50 ml 2N saltsyre til den organiske fase. Eterfasen fraskilles, og saltsyre-fasen utristes fraksjonert med dietyleter ved stigende pH-verdi. Mellom pH 6 og 7,5 samles de fraskilte organiske faser, tørkes med natriumsulfat og inndampes derefter. Example 4 6,7-dimethoxy-1-{2-[N-(4-cyano-4-(4-fluorophenyl)-5-methylhexyl)-N-methylamino]-ethyl}-1-methyl-isochromane (Table 1 , compound no. 10) 8 g of 6,7-dimethoxy-1-methyl-1-[2-(p-tosyloxy)ethyl-isochromane and 5 g of 2-(4-fluorophenyl)-2'-isopropyl-2"-[ 3-(N-methylamino)-propyl]-acetonitrile is dissolved in 50 ml of toluene and stirred for 15 hours at 115° C after the addition of 3 ml of triethylamine and 3 g of potassium carbonate. After evaporation, the residue is taken up in 100 ml of water and extracted with 100 ml diethyl ether. After separation of the water phase, 50 ml of 2N hydrochloric acid is added to the organic phase. The ether phase is separated, and the hydrochloric acid phase is fractionally extracted with diethyl ether at increasing pH values. Between pH 6 and 7.5, the separated organic phases are collected, dried with sodium sulfate and then evaporated.
Derefter foretaes separering over silikagel (Lichroprep Sl 60, kornstørrelse 15 til 25 ym; Merck) med en middeltrykk-kromatografikolonne ifølge Helmchen (G. Helmchen et al.; Angew. Chem. 91, 64 (1979)1 ved 3 til 5 bar. Separation is then carried out over silica gel (Lichroprep Sl 60, grain size 15 to 25 µm; Merck) with a medium pressure chromatography column according to Helmchen (G. Helmchen et al.; Angew. Chem. 91, 64 (1979)1 at 3 to 5 bar).
Efter kromatografisk opparbeidelse fikk man 3,8 g av forbindelsen som en seig, farveløs olje. After chromatographic work-up, 3.8 g of the compound was obtained as a tough, colorless oil.
Eksempel 5 6,7-dimetoksy-4,4-dimetyl-l-{2-[N-(4-cyano-4-(3,4-diklorfenyl)-5-metylheksyl)-N-metylamino]-etyl}isokroman (Tabell 1, forbindelse nr. 11) 2 g 1-(2-kloretyl)-6,7-dimetoksy-4,4'-dimetyl-isokroman omrøres sammen med 2,1 g 2-(3,4-diklorfenyl)-2'-isopropyl-2"-[3-(N-metylamino)-propyl]-acetonitril i 30 ml dimetylformamid med 3 g kaliumkarbonat i 6 timer ved 100°C. Derefter inndampes reaksjonsblandingen og utristes fraksjonert analogt med eksempel 4. Efter fjernelse av eteren separeres de ønskede fraksjoner over silikagel (Lichroprep SI 60, Merck) med en middeltrykk-kromatografikolonne ifølge Helmchen ved 3 til 5 bar. Man oppnår 1,1 g rent stoff som en svakt gulaktig, høyviskøs olje. Eksempel 6 6,7-dimetoksy-l-{1-[N-(4-cyano-4-(3,4-diklorfenyl)-5-metyl-heksyl) -N-metylamino]-metyl}-isokroman (Tabell 1, forbindelse nr. 14) 2 g l-brommetyl-6,7-dimetoksy-isokroman og 2,1 g 2-(3, 4-diklorfenyl)-2'-isopropyl-2"-[3-(N-metylamino)-propyl]-acetonitril oppløses i 30 ml absolutt dimetylformamid. Efter til setning av 3 g kaliumkarbonat omrøres i 15 timer ved 110°C. Reaksjonsproduktet opparbeides analogt med eksempel 4. Man kan isolere 0,6 g av forbindelsen som en seig, farveløs olje. Rf-verdi: 0,54; Elueringsmiddel: CH2C12/CH30H = 9:1 Example 5 6,7-dimethoxy-4,4-dimethyl-1-{2-[N-(4-cyano-4-(3,4-dichlorophenyl)-5-methylhexyl)-N-methylamino]-ethyl}isochromane (Table 1, compound no. 11) 2 g of 1-(2-chloroethyl)-6,7-dimethoxy-4,4'-dimethyl-isochromane are stirred together with 2.1 g of 2-(3,4-dichlorophenyl)- 2'-isopropyl-2"-[3-(N-methylamino)-propyl]-acetonitrile in 30 ml of dimethylformamide with 3 g of potassium carbonate for 6 hours at 100°C. The reaction mixture is then evaporated and fractionally decanted analogously to example 4. After removal of the ether, the desired fractions are separated over silica gel (Lichroprep SI 60, Merck) with a medium-pressure chromatography column according to Helmchen at 3 to 5 bar. 1.1 g of pure substance is obtained as a slightly yellowish, highly viscous oil. Example 6 6.7- Dimethoxy-1-{1-[N-(4-cyano-4-(3,4-dichlorophenyl)-5-methyl-hexyl)-N-methylamino]-methyl}-isochromane (Table 1, compound no. 14) 2 g of 1-bromomethyl-6,7-dimethoxy-isochromane and 2.1 g of 2-(3,4-dichlorophenyl)-2'-isopropyl-2"-[3-(N-methylamino)-propyl]-acetonitrile are dissolved in 30 ml of absolute dimethyl form middle After adding 3 g of potassium carbonate, stir for 15 hours at 110°C. The reaction product is worked up analogously to example 4. One can isolate 0.6 g of the compound as a tough, colorless oil. Rf value: 0.54; Eluent: CH2C12/CH3OH = 9:1
Eksempel 7 Example 7
7,8-dimetoksy-l-{1-[N-(4-(3,4-diklorfenyl)-4-cyano-5-metyl-heksyl)-N-metylamino]-metyl}-l,3,4,5-tetrahydro-2-benzoksepin 7,8-dimethoxy-1-{1-[N-(4-(3,4-dichlorophenyl)-4-cyano-5-methyl-hexyl)-N-methylamino]-methyl}-1,3,4, 5-tetrahydro-2-benzoxepine
(Tabell 1, forbindelse nr. 15)(Table 1, compound no. 15)
2,1 g l-brommetyl-7,8-dimetoksy-l,3,4,5-tetrahydro-2-benzoksepin og 2,1 g 2-(3,4-diklorfenyl)-2'-isopropyl-2"-[3-(N-metylamino)-propyl]-acetonitril oppløses i 30 ml dimetylformamid. Efter tilsetning av 3 g kaliumkarbonat omrøres i 15 timer ved 110°C. Reaksjonsblandingen opparbeides som beskrevet i eksempel 4. 2.1 g of 1-bromomethyl-7,8-dimethoxy-1,3,4,5-tetrahydro-2-benzoxepine and 2.1 g of 2-(3,4-dichlorophenyl)-2'-isopropyl-2"- [3-(N-methylamino)-propyl]-acetonitrile is dissolved in 30 ml of dimethylformamide. After adding 3 g of potassium carbonate, stir for 15 hours at 110° C. The reaction mixture is worked up as described in example 4.
Man får 0,3 g av forbindelsen som en gulaktig, høyviskøs olje. 0.3 g of the compound is obtained as a yellowish, highly viscous oil.
Rf-verdi: 0,55; Elueringsmiddel: CH2C12/CH30H = 9:1 Rf value: 0.55; Eluent: CH2C12/CH3OH = 9:1
Eksempel 8 6,7-dimetoksy-4,4-dimetyl-l-{2-[N-(4-cyano-4-(4-fluorfenyl)-5-metylheksyl)-N-metylamino]-etyl}-isokroman (Tabell 1, forbindelse nr. 19) 2 g 1-(2-kloretyl)-6,7-dimetoksy-4,4<1->dimetyl-isokroman oppløses sammen med 1,8 g 2- (4-fluorfenyl)-2'-isopropyl-2"-[3-(N-metylamino)-propyl]-acetonitril i 30 ml dimetylformamid. Derefter tilsettes 3 g kaliumkarbonat, og det hele omrøres 6 timer ved 100°C. Efter avkjøling opptaes reaksjonsproduktet i vann og 2N saltsyre. Ved stigende pH-verdi foretaes fraksjonert utristning med dietyleter. Deønskede fraksjoner opp- Example 8 6,7-dimethoxy-4,4-dimethyl-1-{2-[N-(4-cyano-4-(4-fluorophenyl)-5-methylhexyl)-N-methylamino]-ethyl}-isochroman ( Table 1, compound no. 19) 2 g of 1-(2-chloroethyl)-6,7-dimethoxy-4,4<1->dimethyl-isochromane are dissolved together with 1.8 g of 2-(4-fluorophenyl)-2 '-isopropyl-2"-[3-(N-methylamino)-propyl]-acetonitrile in 30 ml of dimethylformamide. Then 3 g of potassium carbonate are added, and the whole is stirred for 6 hours at 100°C. After cooling, the reaction product is taken up in water and 2N hydrochloric acid. If the pH value rises, fractional extraction is carried out with diethyl ether. The desired fractions up-
arbeides kromatografisk som beskrevet i eksempel 1.is worked on chromatographically as described in example 1.
Efter den kromatografiske separering kunne 0,8 g ren forbindelse isoleres som en farveløs olje. After the chromatographic separation, 0.8 g of pure compound could be isolated as a colorless oil.
Rf-verdi: 0,52; Elueringsmiddel: CH2C12/'CH30H = 8:2 Rf value: 0.52; Eluent: CH 2 Cl 2 /CH 3 OH = 8:2
Eksempel 9 Example 9
6,7-dimetoksy-l-{2-[N—(4-cyano-5-metyl-4-(3,4,5-trimetoksy-fenyl)heksyl)-N-metylamino]-etyl}-isokroman (Tabell 1, forbindelse nr. 26) 6,7-dimethoxy-1-{2-[N-(4-cyano-5-methyl-4-(3,4,5-trimethoxy-phenyl)hexyl)-N-methylamino]-ethyl}-isochromane (Table 1, connection no. 26)
1,8 g 1-(2-kloretyi)-6,7-dimetoksy-isokroman og 2,1 g 2-isopropyl-2<1->[3-(N-metylamino)-propyl]-2"-(3,4,5-trimetoksy-fenyl)-acetonitril oppløses i 30 ml absolutt dimetylformamid og omrøres natten over ved 100°C efter tilsetning av 10 ml trietylamin og 3 g kaliumkarbonat. Efter fjernelse av opp-løsningsmidlet i vakuum tilsettes 150 ml dietyleter og 100 ml vann og utristes. Den organiske fase utristes 3 ganger med 80 ml 2N saltsyre hver gang. De saltsure, vandige faser samles og nøytraliseres derefter med soda. Derefter ekstraheres med 100 ml dietyleter. Den organiske fase tørkes over natriumsulfat og inndampes deretter. Residuet separeres kromatografisk over en silikagel-kolonne (se eksempel 1). 1.8 g of 1-(2-chloroethyl)-6,7-dimethoxy-isochromane and 2.1 g of 2-isopropyl-2<1->[3-(N-methylamino)-propyl]-2"-(3 ,4,5-trimethoxy-phenyl)-acetonitrile is dissolved in 30 ml of absolute dimethylformamide and stirred overnight at 100° C. after adding 10 ml of triethylamine and 3 g of potassium carbonate. After removing the solvent in vacuo, 150 ml of diethyl ether and 100 ml of water and decanted. The organic phase is decanted 3 times with 80 ml of 2N hydrochloric acid each time. The hydrochloric acid, aqueous phases are collected and then neutralized with soda. Then extracted with 100 ml of diethyl ether. The organic phase is dried over sodium sulfate and then evaporated. The residue is separated chromatographically over a silica gel column (see example 1).
Man får 0,9 g av forbindelsen som en gulaktig, seig olje. 0.9 g of the compound is obtained as a yellowish, viscous oil.
Rf-verdi: 0,42; Elueringsmiddel: CH2Cl2/CH3CN/C2H5OH = Rf value: 0.42; Eluent: CH2Cl2/CH3CN/C2H5OH =
7:2:1 7:2:1
Eksempel 10 Example 10
6 , 7-dimetoksy-l-{ 2- [N- (4-cyano-5-metyl-4 (3 , 4-metylen-dioksyf enyl-)-heksyl)-N-metylamino]-etyl}-4-metyl-isokroman (Tabell 1, forbindelse nr. 28) 6,7-dimethoxy-1-{2-[N-(4-cyano-5-methyl-4(3,4-methylene-dioxyphenyl-)-hexyl)-N-methylamino]-ethyl}-4-methyl -isochrome (Table 1, compound no. 28)
1,9 g 1-(2-kloroetyll-6,7-dimetoksy-4-metyl-isokroman1.9 g 1-(2-chloroethyl-6,7-dimethoxy-4-methyl-isochromane)
og 1,9 g 2-isopropy1-2'-(3,4-metylendioksyfenyl)-2"-[3-(N-metylamino)-propyl]-acetonitril oppløses i 10 ml absolutt dimetylformamid og omrøres ved 100°C i 15 timer efter til- and 1.9 g of 2-isopropyl-2'-(3,4-methylenedioxyphenyl)-2"-[3-(N-methylamino)-propyl]-acetonitrile are dissolved in 10 ml of absolute dimethylformamide and stirred at 100°C for 15 hours after to-
setning av 20 ml trietylamin og 3 g kaliumkarbonat. Derefter opparbeides som beskrevet i eksempel 9. addition of 20 ml of triethylamine and 3 g of potassium carbonate. It is then processed as described in example 9.
Man får 250 mg av forbindelsen som en seig, farveløs olje. You get 250 mg of the compound as a tough, colorless oil.
Rf-verdi: 0,41; Elueringsmiddel: CH2C12/CH30H = 9:1 Rf value: 0.41; Eluent: CH2C12/CH3OH = 9:1
Eksempel 11 Example 11
6,7-dimetoksy-l-{2-[N-(4-cyano-5-metyl-4-(3,4,5-trimetoksy-fenyl)heksyl)-N-metylamino]-metyl}-l,4,4-trimetyl-isokroman 6,7-dimethoxy-1-{2-[N-(4-cyano-5-methyl-4-(3,4,5-trimethoxy-phenyl)hexyl)-N-methylamino]-methyl}-1,4 ,4-trimethylisochrome
(Tabell 1, forbindelse nr. 29)(Table 1, compound no. 29)
3,4 g 1-(2-brometyl)-6,7-dimetoksy-l,4,4'-trimetyl-isokroman og 3,1 g 2-isopropyl-2'-[3-(N-metylamino)-propyl]-2"-(3,4,5-trimetoksyfenyl)-acetonitril oppløses i 15 ml dimetylformamid og omrøres ved 120°C i 12 timer efter tilsetning av 30 ml trietylamin og 3 g kaliumkarbonat. Derefter utristes fraksjonert analogt med eksempel 1. De ønskede fraksjoner (pH 6 til pH 7,5) samles. Eterfasen tørkes og fjernes derefter. Råproduktet renses kromatografisk. 3.4 g of 1-(2-bromomethyl)-6,7-dimethoxy-1,4,4'-trimethyl-isochromane and 3.1 g of 2-isopropyl-2'-[3-(N-methylamino)-propyl ]-2"-(3,4,5-trimethoxyphenyl)-acetonitrile is dissolved in 15 ml of dimethylformamide and stirred at 120°C for 12 hours after the addition of 30 ml of triethylamine and 3 g of potassium carbonate. Then fractionally extracted analogously to example 1. The desired fractions (pH 6 to pH 7.5) are collected.The ether phase is dried and then removed.The crude product is purified chromatographically.
Efter kromatografisk opparbeidelse oppnåes 1,9 g av forbindelsen som en lyst gulaktig, seig olje. After chromatographic work-up, 1.9 g of the compound is obtained as a pale yellowish, viscous oil.
Rf-verdi: 0,34; Elueringsmiddel: CH2Cl2/CH3OH = 9:1 Rf value: 0.34; Eluent: CH2Cl2/CH3OH = 9:1
Eksempel 12 Example 12
6,7-dimetoksy-l-{2-[N-(4-cyano-4-(4-fluorfenyl)-5-metylheksyl)-N-metylamino]-etyl}-l,4,4-trimetyl-isokroman (Tabell 1, forbindelse nr. 31) 6,7-dimethoxy-1-{2-[N-(4-cyano-4-(4-fluorophenyl)-5-methylhexyl)-N-methylamino]-ethyl}-1,4,4-trimethyl-isochromane ( Table 1, compound no. 31)
3,4 g 1-(2-brometyl)-6,7-dimetoksy-l,4,4'-trimetyl)-isokroman, 2,5 g 2-(4-fluorfenyl)-2'-isopropyl-2"-[3-(N-metylamino) -propyl]-acetonitril, 20 ml trietylamin og 3 g kaliumkarbonat omsettes på samme måte i eksempel 1 og opparbeides. Efter den kromatografiske opparbeidelse kunne 1,8 g rent produkt oppnåes som en farveløs, høyviskøs olje. 3.4 g 1-(2-bromomethyl)-6,7-dimethoxy-1,4,4'-trimethyl)-isochromane, 2.5 g 2-(4-fluorophenyl)-2'-isopropyl-2"- [3-(N-methylamino)-propyl]-acetonitrile, 20 ml of triethylamine and 3 g of potassium carbonate are reacted and worked up in the same way as in Example 1. After the chromatographic work-up, 1.8 g of pure product could be obtained as a colorless, highly viscous oil.
Rf-verdi: 0,36; Elueringsmiddel: CH2C12/CH30H = 9:1 Rf value: 0.36; Eluent: CH2C12/CH3OH = 9:1
Eksempel 13 Example 13
6,7-dimetoksy-l-{2-[N-(4-cyano-5-metyl-4-(3-trifluormetylfenyl)-heksyl)-N-metylamino]-etyl}-isokroman (Tabell 1, forbindelse nr. 33) 6,7-dimethoxy-1-{2-[N-(4-cyano-5-methyl-4-(3-trifluoromethylphenyl)-hexyl)-N-methylamino]-ethyl}-isochromane (Table 1, compound no. 33)
1,8 g 1-(2-kloretyl)-6,7-dimetoksy-isokroman, 2,1 g 2-isopropyl-2 1 - [3- (N-metylamino )_-propyl] -2"- (3-trif luorf enyl) - acetonitril, 10 ml dimetylformamid, 20 ml trietylamin og 3 g kaliumkarbonat omsettes analogt med eksempel 1 og opparbeides. 1.8 g 1-(2-chloroethyl)-6,7-dimethoxy-isochromane, 2.1 g 2-isopropyl-2 1 -[3-(N-methylamino)_-propyl]-2"-(3- trifluorophenyl) - acetonitrile, 10 ml of dimethylformamide, 20 ml of triethylamine and 3 g of potassium carbonate are reacted analogously to example 1 and worked up.
Efter kromatografisk separering kunne 0,8 g rent produkt isoleres som en farveløs, seig olje. After chromatographic separation, 0.8 g of pure product could be isolated as a colorless, viscous oil.
Rf-verdi: 0,42; Elueringsmiddel: CH2<C1>2</>CH30H = 9:1Rf value: 0.42; Eluent: CH2<C1>2</>CH3OH = 9:1
Eksempel 14 6,7-dimetoksy-l-{2-[N-(4-cyano-4-(3,4-dimetoksyfenyl)-5-metyl-heksyl ) -N-metylamino] -etyl }-l-metyl-isokroman (Tabell 1, forbindelse nr. 35) 4 g 6,7-dimetoksy-l-metyl-l-[2-(p-tosyloksy)-etyl]-isokroman og 2,9 g 2-(3,4-dimetoksyfenyl)-2<1->isopropyl-2"-[3-(N-metylamino)-propyl]-acetonitril oppløses i 30 ml tørr toluen og 5 ml dimetylformamid og omrøres ved 100°C i 15 timer efter tilsetning av 5 ml trietylamin og 3 g kaliumkarbonat. Opp-arbeidelsen skjer analogt med eksempel 4. Efter den kromatografiske separering over silikagel får man 3,1 g av forbindelsen som en høyviskøs, farveløs olje. Example 14 6,7-dimethoxy-1-{2-[N-(4-cyano-4-(3,4-dimethoxyphenyl)-5-methyl-hexyl)-N-methylamino]-ethyl}-1-methyl- isochromane (Table 1, compound no. 35) 4 g of 6,7-dimethoxy-1-methyl-1-[2-(p-tosyloxy)-ethyl]-isochromane and 2.9 g of 2-(3,4-dimethoxyphenyl) )-2<1->isopropyl-2"-[3-(N-methylamino)-propyl]-acetonitrile is dissolved in 30 ml of dry toluene and 5 ml of dimethylformamide and stirred at 100°C for 15 hours after the addition of 5 ml of triethylamine and 3 g of potassium carbonate. The work-up takes place analogously to example 4. After the chromatographic separation over silica gel, 3.1 g of the compound is obtained as a highly viscous, colorless oil.
Rf-verdi: 0,21; Elueringsmiddel: CH2C<l>2OCH3OH = 9:1Rf value: 0.21; Eluent: CH2C<1>2OCH3OH = 9:1
Claims (3)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19843409612 DE3409612A1 (en) | 1984-03-16 | 1984-03-16 | NEW SUBSTITUTED ISOCHROMANS AND OXEPINES, THEIR ACID ADDITIONAL SALTS, THE MEDICINAL PRODUCTS CONTAINING THEM AND METHOD FOR THE PRODUCTION THEREOF |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| NO851029L true NO851029L (en) | 1985-09-17 |
Family
ID=6230653
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO851029A NO851029L (en) | 1984-03-16 | 1985-03-15 | ANALOGY PROCEDURE FOR THE PREPARATION OF THERAPEUTICALLY ACTIVE ISOCHROMAN AND OCSEPIN DERIVATIVES |
Country Status (18)
| Country | Link |
|---|---|
| EP (1) | EP0157206A3 (en) |
| JP (1) | JPS60209581A (en) |
| KR (1) | KR850006397A (en) |
| AU (1) | AU4001785A (en) |
| CS (1) | CS247196B2 (en) |
| DD (1) | DD234421A5 (en) |
| DE (1) | DE3409612A1 (en) |
| DK (1) | DK120185A (en) |
| ES (1) | ES8606324A1 (en) |
| FI (1) | FI851022L (en) |
| GR (1) | GR850658B (en) |
| HU (1) | HUT37419A (en) |
| IL (1) | IL74616A0 (en) |
| NO (1) | NO851029L (en) |
| PH (1) | PH20880A (en) |
| PL (1) | PL252375A1 (en) |
| PT (1) | PT80115B (en) |
| ZA (1) | ZA851948B (en) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3642331A1 (en) * | 1986-12-11 | 1988-06-23 | Basf Ag | BASICLY SUBSTITUTED PHENYL ACETONITRILES, THEIR PRODUCTION AND THE MEDICINAL PRODUCTS CONTAINING THEM |
| JPH03178952A (en) * | 1989-06-23 | 1991-08-02 | Kyowa Hakko Kogyo Co Ltd | Arylalkylamine derivative |
| EP0450689A1 (en) * | 1990-04-02 | 1991-10-09 | Akzo Nobel N.V. | New isochromane derivatives |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB1552004A (en) * | 1976-05-26 | 1979-09-05 | Takeda Chemical Industries Ltd | Isochroman derivatives |
-
1984
- 1984-03-16 DE DE19843409612 patent/DE3409612A1/en not_active Withdrawn
-
1985
- 1985-03-06 EP EP85102518A patent/EP0157206A3/en not_active Withdrawn
- 1985-03-14 DD DD85274121A patent/DD234421A5/en unknown
- 1985-03-14 CS CS851778A patent/CS247196B2/en unknown
- 1985-03-14 PL PL25237585A patent/PL252375A1/en unknown
- 1985-03-14 GR GR850658A patent/GR850658B/el unknown
- 1985-03-14 KR KR1019850001630A patent/KR850006397A/en not_active Withdrawn
- 1985-03-14 FI FI851022A patent/FI851022L/en not_active Application Discontinuation
- 1985-03-15 DK DK120185A patent/DK120185A/en unknown
- 1985-03-15 ES ES541295A patent/ES8606324A1/en not_active Expired
- 1985-03-15 HU HU85975A patent/HUT37419A/en unknown
- 1985-03-15 ZA ZA851948A patent/ZA851948B/en unknown
- 1985-03-15 JP JP60050718A patent/JPS60209581A/en active Pending
- 1985-03-15 NO NO851029A patent/NO851029L/en unknown
- 1985-03-15 IL IL74616A patent/IL74616A0/en unknown
- 1985-03-15 PT PT80115A patent/PT80115B/en unknown
- 1985-03-15 AU AU40017/85A patent/AU4001785A/en not_active Abandoned
- 1985-03-18 PH PH31999A patent/PH20880A/en unknown
Also Published As
| Publication number | Publication date |
|---|---|
| IL74616A0 (en) | 1985-06-30 |
| ES541295A0 (en) | 1986-04-01 |
| CS247196B2 (en) | 1986-12-18 |
| PL252375A1 (en) | 1985-10-22 |
| ES8606324A1 (en) | 1986-04-01 |
| FI851022A0 (en) | 1985-03-14 |
| JPS60209581A (en) | 1985-10-22 |
| EP0157206A2 (en) | 1985-10-09 |
| HUT37419A (en) | 1985-12-28 |
| PH20880A (en) | 1987-05-27 |
| DD234421A5 (en) | 1986-04-02 |
| AU4001785A (en) | 1985-09-19 |
| DK120185A (en) | 1985-09-17 |
| ZA851948B (en) | 1986-11-26 |
| PT80115B (en) | 1987-03-24 |
| PT80115A (en) | 1985-04-01 |
| EP0157206A3 (en) | 1986-06-11 |
| DK120185D0 (en) | 1985-03-15 |
| KR850006397A (en) | 1985-10-05 |
| FI851022A7 (en) | 1985-09-17 |
| GR850658B (en) | 1985-07-11 |
| FI851022L (en) | 1985-09-17 |
| DE3409612A1 (en) | 1985-09-19 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| RU2091379C1 (en) | Diphenylmethylpiperazine derivatives or their pharmaceutically acceptable salt | |
| NO155490B (en) | ANALOGUE PROCEDURE FOR THE PREPARATION OF THERAPEUTIC ACTIVITY 4-) 1 "-HYDROXY-2" - (N-IMIDAZOLYL) ETHYL) BIBENZYL. | |
| US4889858A (en) | Dibenz[b,e]oxepin derivatives and pharmaceutical composition containing the same | |
| US4935414A (en) | New indolylpropanols, processes for their preparation and their use, and preparations containing the compounds | |
| CA2214744C (en) | 3-(bis-substituted phenylmethylene)oxindole derivatives | |
| AU610294B2 (en) | Amino acid esters of 4-alkoxy-5-arylhydroxymethyl-2-(5h)- furanone | |
| NO149502B (en) | ANALOGUE PROCEDURE FOR THE PREPARATION OF PHYSIOLOGICALLY ACTIVE AMINOAL COCOXYPHENYL DERIVATIVES. | |
| JPH01106839A (en) | Alkadiene derivatives, manufacture and pharmacological composition | |
| CZ279282B6 (en) | Process for preparing 1-/(diarylmethoxy)-alkyl/pyrrolidines and piperidines | |
| US4140790A (en) | 3-(4-Substituted piperazino)-1-xanthene-9-carbonyloxy-propanes | |
| GB2171997A (en) | 4-Amino-6,7-dimethoxy-2-Piperazin-1-ylquinazoline derivatives | |
| DK167974B1 (en) | 1- (PHENYLALKYL) -3- (3-HYDROXYPHENYL) PIPERIDINE COMPOUNDS PROCEDURES FOR PREPARING THEREOF AND 3- (3-METHOXYPHENYLPYRIPERIDINE COMPOUNDS FOR THE USE OF INTERMEDIATE PRODUCTS | |
| US4191770A (en) | N1 -acyl-N2 -phenyldiaminopropanols and pharmaceutical compositions thereof | |
| NO820291L (en) | ANALOGY PROCEDURE FOR THE PREPARATION OF THERAPEUTICALLY ACTIVE ALKANOLAMINE DERIVATIVES | |
| SU893133A3 (en) | Method of preparing derivatives of 1-/3-(3,4,5-trimethoxyphenoxy)-2-propyl/-4-arylpiperazine | |
| EP0071175B1 (en) | Phenylalkyloxirane-carboxylic acids, process for their preparation, their use and medicines containing them | |
| KR910006987B1 (en) | Method for preparing aminoethyl imidazole | |
| Chapman et al. | Synthesis and 13C NMR spectra of cis‐and trans‐{2‐(haloaryl)‐2‐[(1H‐imidazol)‐1‐yl] methyl]}‐1, 3‐dioxolane‐4‐methanols | |
| Albrecht et al. | Enantio-and Diastereoselective Synthesis of β, γ, γ, δ-Tetrasubstituted α-Methylene-δ-lactones | |
| EP0481253B1 (en) | p-Oxybenzoic acid derivatives, process for preparing them, and their use as medicaments | |
| CS247196B2 (en) | Method of new substituted isochromates and oxopines production | |
| CA2117075A1 (en) | Quinazoline derivatives and their preparation | |
| RU2204556C2 (en) | Method of synthesis of 1-(para-chlorobenzhydryl)-4-(2-hydroxyethyl)-piperazine | |
| HU186488B (en) | Process for producing pyridine derivatives and pharmaceutival compositions containing them as active agents | |
| EP0529226B1 (en) | p-Oxybenzoic acid derivatives, process for preparing them and their use as medicaments |