CA2063030A1 - Substituted n-phenylpiperidines and drugs therefrom - Google Patents
Substituted n-phenylpiperidines and drugs therefromInfo
- Publication number
- CA2063030A1 CA2063030A1 CA002063030A CA2063030A CA2063030A1 CA 2063030 A1 CA2063030 A1 CA 2063030A1 CA 002063030 A CA002063030 A CA 002063030A CA 2063030 A CA2063030 A CA 2063030A CA 2063030 A1 CA2063030 A1 CA 2063030A1
- Authority
- CA
- Canada
- Prior art keywords
- see formula
- substituted
- radicals
- alkyl
- phenylpiperidines
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 239000003814 drug Substances 0.000 title abstract 2
- 229940079593 drug Drugs 0.000 title abstract 2
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 3
- 150000003254 radicals Chemical class 0.000 abstract 3
- -1 NH-CHO Chemical compound 0.000 abstract 2
- 229910052736 halogen Inorganic materials 0.000 abstract 2
- 150000002367 halogens Chemical class 0.000 abstract 2
- 230000003287 optical effect Effects 0.000 abstract 2
- JCXJVPUVTGWSNB-UHFFFAOYSA-N Nitrogen dioxide Chemical compound O=[N]=O JCXJVPUVTGWSNB-UHFFFAOYSA-N 0.000 abstract 1
- 239000002253 acid Substances 0.000 abstract 1
- 125000002485 formyl group Chemical group [H]C(*)=O 0.000 abstract 1
- CBOIHMRHGLHBPB-UHFFFAOYSA-N hydroxymethyl Chemical compound O[CH2] CBOIHMRHGLHBPB-UHFFFAOYSA-N 0.000 abstract 1
- 125000000896 monocarboxylic acid group Chemical group 0.000 abstract 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 abstract 1
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 abstract 1
Classifications
-
- 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
- C07D401/04—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 directly linked by a ring-member-to-ring-member bond
-
- 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
- A61P9/06—Antiarrhythmics
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D211/00—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
- C07D211/04—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D211/06—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
- C07D211/08—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms
- C07D211/18—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms with substituted hydrocarbon radicals attached to ring carbon atoms
- C07D211/26—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms with substituted hydrocarbon radicals attached to ring carbon atoms with hydrocarbon radicals, substituted by nitrogen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D211/00—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
- C07D211/04—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D211/06—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
- C07D211/36—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D211/56—Nitrogen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D211/00—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
- C07D211/04—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D211/06—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
- C07D211/36—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D211/56—Nitrogen atoms
- C07D211/58—Nitrogen atoms attached in position 4
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Life Sciences & Earth Sciences (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Pharmacology & Pharmacy (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Hydrogenated Pyridines (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
Abstract
Substituted N-phenylpiperid-ines I
(see formula I) (R1 = H, NO2, CN, halogen, C1-C4-alkyl, CF3, OCF3, OH, CH2OH, COOH, CHO, NH-CHO, NH2, CO-NH2, 5-tetrazinyl, R4-O-, R4-O-CH2-, R4-O-CO-, R4-CO-, R4-NH-CO, R4-CO-NH-, R4-SO2-NH-;
R2 = H, NO2, halogen, C1-C4-alkyl or R4-O-;
(see formula II) (see formula III) (see formula IV) (see formula V) (see formula VI) (see formula VII) (see formula VIII) R4 = C1-C4-alkyl or phenyl which can carry one of the R2 radicals;
R5, R6, H or one of the R4 radicals; R7 = one of the R1 radicals;
n = 0 or 1; m = 1 or 2;
with the proviso that R3 is (see formula IX) only when n is 1, and the optical isomers in the case of optical isomerism, and the physiologically tolerated acid addition salts, are suitable as drugs.
(see formula I) (R1 = H, NO2, CN, halogen, C1-C4-alkyl, CF3, OCF3, OH, CH2OH, COOH, CHO, NH-CHO, NH2, CO-NH2, 5-tetrazinyl, R4-O-, R4-O-CH2-, R4-O-CO-, R4-CO-, R4-NH-CO, R4-CO-NH-, R4-SO2-NH-;
R2 = H, NO2, halogen, C1-C4-alkyl or R4-O-;
(see formula II) (see formula III) (see formula IV) (see formula V) (see formula VI) (see formula VII) (see formula VIII) R4 = C1-C4-alkyl or phenyl which can carry one of the R2 radicals;
R5, R6, H or one of the R4 radicals; R7 = one of the R1 radicals;
n = 0 or 1; m = 1 or 2;
with the proviso that R3 is (see formula IX) only when n is 1, and the optical isomers in the case of optical isomerism, and the physiologically tolerated acid addition salts, are suitable as drugs.
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE4108184 | 1991-03-14 | ||
DEP4108184.6 | 1991-03-14 | ||
DE4117904A DE4117904A1 (en) | 1991-05-31 | 1991-05-31 | SUBSTITUTED N-PHENYLPIPERIDINES |
DEP4117904.8 | 1991-05-31 |
Publications (2)
Publication Number | Publication Date |
---|---|
CA2063030A1 true CA2063030A1 (en) | 1992-09-15 |
CA2063030C CA2063030C (en) | 2002-03-26 |
Family
ID=25901832
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CA002063030A Expired - Fee Related CA2063030C (en) | 1991-03-14 | 1992-03-13 | Substituted n-phenylpiperidines and drugs therefrom |
Country Status (5)
Country | Link |
---|---|
EP (1) | EP0503411B1 (en) |
JP (1) | JP3058746B2 (en) |
AT (1) | ATE130851T1 (en) |
CA (1) | CA2063030C (en) |
DE (1) | DE59204456D1 (en) |
Families Citing this family (15)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6184236B1 (en) | 1998-08-18 | 2001-02-06 | Hoffmann-La Roche Inc. | Method of treating a neurodegenerative disease by administering an aryl-cyclohexylamine derivative |
EP0982026B1 (en) * | 1998-08-18 | 2006-05-17 | F. Hoffmann-La Roche Ag | Use of aryl-cyclohexylamine derivatives in the manufacture of NMDA receptor blockers |
US7592450B2 (en) * | 2002-03-13 | 2009-09-22 | Janssen Pharmaceutica N.V. | Piperazinyl-, piperidinyl- and morpholinyl-derivatives as inhibitors of histone deacetylase |
JP4765627B2 (en) * | 2003-09-22 | 2011-09-07 | Msd株式会社 | Novel piperidine derivatives |
AR047759A1 (en) | 2003-09-26 | 2006-02-22 | Vertex Pharma | FENIL DERIVATIVES - PIPERAZINE AS MODULATORS OF MUSCARNIC RECEPTORS |
CA2625153A1 (en) | 2005-10-21 | 2007-04-26 | Braincells, Inc. | Modulation of neurogenesis by pde inhibition |
AU2006308889A1 (en) | 2005-10-31 | 2007-05-10 | Braincells, Inc. | GABA receptor mediated modulation of neurogenesis |
US20100216734A1 (en) | 2006-03-08 | 2010-08-26 | Braincells, Inc. | Modulation of neurogenesis by nootropic agents |
AU2007249435A1 (en) | 2006-05-09 | 2007-11-22 | Braincells, Inc. | 5 HT receptor mediated neurogenesis |
WO2007134136A2 (en) | 2006-05-09 | 2007-11-22 | Braincells, Inc. | Neurogenesis by modulating angiotensin |
US20100184806A1 (en) | 2006-09-19 | 2010-07-22 | Braincells, Inc. | Modulation of neurogenesis by ppar agents |
WO2010081851A1 (en) | 2009-01-14 | 2010-07-22 | Genoscience Pharma | Piperidin-4-ylpiperazine compounds for the treatment of hcv infection |
WO2010099217A1 (en) | 2009-02-25 | 2010-09-02 | Braincells, Inc. | Modulation of neurogenesis using d-cycloserine combinations |
JP5187534B2 (en) * | 2010-02-12 | 2013-04-24 | 有機合成薬品工業株式会社 | Process for producing N-tert-butoxycarbonyl-4-formylpiperidine |
WO2014140671A1 (en) * | 2013-03-15 | 2014-09-18 | Institut De Recherche Pour Le Developpement | New arylaminoalcohol derivatives with antiplasmodial activity |
Family Cites Families (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE749887C (en) * | 1941-10-02 | 1944-12-20 | Process for the preparation of substituted 4-aminopiperidines | |
DK78744C (en) * | 1949-07-20 | 1955-01-17 | Knoll Ag | Process for the preparation of 4- (N-phenyl-N-benzyl) -amino-1-alkylpiperidines or their derivatives substituted in the aromatic radicals. |
GB1077173A (en) * | 1965-03-19 | 1967-07-26 | American Cyanamid Co | Substituted alkylene piperidines and methods of preparation thereof |
NL6703315A (en) * | 1966-03-22 | 1967-09-25 | ||
EP0097000B1 (en) * | 1982-06-10 | 1987-09-09 | Beecham Wuelfing GmbH & Co KG | Amine derivatives |
US4902800A (en) * | 1988-08-17 | 1990-02-20 | American Home Products Corporation | 1-Substituted-4-pyrrolidinopiperidines as inhibitors of interleukin 1 |
DE4032766A1 (en) * | 1990-10-16 | 1992-04-30 | Basf Ag | PHENYLPIPERIDINOYLAMINE AND MEDICINAL PRODUCTS CONTAINING THEM |
-
1992
- 1992-02-29 AT AT92103514T patent/ATE130851T1/en not_active IP Right Cessation
- 1992-02-29 EP EP92103514A patent/EP0503411B1/en not_active Expired - Lifetime
- 1992-02-29 DE DE59204456T patent/DE59204456D1/en not_active Expired - Fee Related
- 1992-03-13 JP JP4055006A patent/JP3058746B2/en not_active Expired - Lifetime
- 1992-03-13 CA CA002063030A patent/CA2063030C/en not_active Expired - Fee Related
Also Published As
Publication number | Publication date |
---|---|
JPH0578316A (en) | 1993-03-30 |
ATE130851T1 (en) | 1995-12-15 |
JP3058746B2 (en) | 2000-07-04 |
EP0503411B1 (en) | 1995-11-29 |
CA2063030C (en) | 2002-03-26 |
EP0503411A1 (en) | 1992-09-16 |
DE59204456D1 (en) | 1996-01-11 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CA2063030A1 (en) | Substituted n-phenylpiperidines and drugs therefrom | |
TW568896B (en) | Calcium receptor-active compounds | |
FI914928A0 (en) | HYDROXIMETHYL (METHYLENCYCLOPENTYL) PURINER OCH -PYRIMIDINER. | |
FI931250A (en) | SULPHONAMIDO-OCH SULFONAMIDOCARBONYL-PYRIDIN-2-CARBOXYLSYRAMIDER OCH DERASE PYRIDINE-N-OXIDER, FOERFARANDE FOER DERAS FRAMSTAELLNING OCH DERAS ANVAENDNING SOM LAEKEMEDEL | |
HUP0301330A2 (en) | 2-aminocarbonyl-9h-purine derivatives | |
MX9201760A (en) | QUINOXALINS, PROCEDURE FOR ITS PREPARATION AND EMPLOYMENT. | |
DK0496222T3 (en) | indole derivatives | |
NO951529L (en) | 3 indolylpiperidiner | |
ATE129236T1 (en) | N-SULPHONYLINDOLINE DERIVATIVES, THEIR PRODUCTION AND MEDICINAL PRODUCTS CONTAINING THEM. | |
EP0481299A3 (en) | N-phenyl-piperidyl-4-amines and drugs containing them | |
FI924839A0 (en) | CYCLIC HYDROXAMSYROR OCH ANVAENDNING AV DEM | |
TR199501158A2 (en) | Quinoxaline derivatives that are particularly useful in the treatment of neurodegenerative disorders. | |
ID16479A (en) | COMPOUND TREATMENTS | |
ATE522501T1 (en) | PHENOLIC COMPOUNDS AND RECORDING MATERIALS CONTAINING THEM | |
DE69515402D1 (en) | Oxazoloquinolinone derivatives, their preparation and their use as medicines | |
IT1251202B (en) | 6-AMINOKINOLONES, SYNTHESIS AND USE AS ANTIBACTERIALS | |
ATE123025T1 (en) | 2-AMINO-N-(((4-(AMINOCARBONYL)PYRIMIDINE-2- YL>AMINO>ALKYL>-PYRIMIDINE-4- CARBOXYLIC AMIDE DERIVATIVES, THEIR PRODUCTION AND THEIR APPLICATION IN THERAPEUTICS. | |
AU4475993A (en) | Carbamic acid derivatives | |
ATE252558T1 (en) | 1-AZA-2-ALKYL-6-ARYL-CYCLOALKANES TO IMPROVE MEMORY | |
ES2093051T3 (en) | PURINIL- AND PIRIMIDIL-TETRAHIDROFURANOS. | |
NO922523D0 (en) | AMINOPYRIMIDINE CARBOXAMIDE DERIVATIVES WITH THERAPEUTIC EFFECT | |
SU1690339A1 (en) | N- (3-CHLORO-1,4-NAFTOKHINONIL-2) -2-D, L-ASPARAGIC ACID, DISPLAYING CARDIOSTIMULATING PROPERTIES | |
DK0483063T3 (en) | ergoline | |
TH13138EX (en) | Pipersinil and Piperidinyl cyclohexanol | |
TH8094S (en) | Washable faucet |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
EEER | Examination request | ||
MKLA | Lapsed |