WO1993014084A3 - Piperidine derivatives - Google Patents
Piperidine derivatives Download PDFInfo
- Publication number
- WO1993014084A3 WO1993014084A3 PCT/EP1993/000101 EP9300101W WO9314084A3 WO 1993014084 A3 WO1993014084 A3 WO 1993014084A3 EP 9300101 W EP9300101 W EP 9300101W WO 9314084 A3 WO9314084 A3 WO 9314084A3
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- alkyl
- represents hydrogen
- 4alkoxy
- piperidine derivatives
- relates
- Prior art date
Links
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
- C07D401/06—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
Abstract
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB9201179.0 | 1992-01-21 | ||
GB929201179A GB9201179D0 (en) | 1992-01-21 | 1992-01-21 | Chemical compounds |
Publications (2)
Publication Number | Publication Date |
---|---|
WO1993014084A2 WO1993014084A2 (en) | 1993-07-22 |
WO1993014084A3 true WO1993014084A3 (en) | 1993-10-14 |
Family
ID=10708912
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/EP1993/000101 WO1993014084A2 (en) | 1992-01-21 | 1993-01-15 | Piperidine derivatives |
Country Status (4)
Country | Link |
---|---|
AU (1) | AU3351393A (en) |
GB (1) | GB9201179D0 (en) |
IL (1) | IL104445A0 (en) |
WO (1) | WO1993014084A2 (en) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US9034899B2 (en) | 2009-05-12 | 2015-05-19 | Albany Molecular Research, Inc. | Aryl, heteroaryl, and heterocycle substituted tetrahydroisoquinolines and use thereof |
US9156812B2 (en) | 2008-06-04 | 2015-10-13 | Bristol-Myers Squibb Company | Crystalline form of 6-[(4S)-2-methyl-4-(2-naphthyl)-1,2,3,4-tetrahydroisoquinolin-7-yl]pyridazin-3-amine |
US9173879B2 (en) | 2009-05-12 | 2015-11-03 | Bristol-Myers Squibb Company | Crystalline forms of (S)-7-([1,2,4]triazolo[1,5-a ]pyridin-6-yl)-4-(3,4-dichlorophenyl)-1,2,3,4-tetrahydroisoquinoline and use thereof |
US9499531B2 (en) | 2004-07-15 | 2016-11-22 | Albany Molecular Research, Inc. | Aryl- and heteroaryl-substituted tetrahydroisoquinolines and use thereof to block reuptake of norepinephrine, dopamine, and serotonin |
Families Citing this family (58)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2700472B1 (en) | 1993-01-19 | 1995-02-17 | Rhone Poulenc Rorer Sa | Synergizing association having an antagonistic effect on the NK1 and NK2 receptors. |
EP0653208A3 (en) * | 1993-11-17 | 1995-10-11 | Pfizer | Pharmaceutical agents for treatment or prevention of sunburn. |
US5610165A (en) * | 1994-02-17 | 1997-03-11 | Merck & Co., Inc. | N-acylpiperidine tachykinin antagonists |
FR2719476B1 (en) * | 1994-05-05 | 1997-05-23 | Oreal | Use of a substance P antagonist in a cosmetic composition and composition obtained. |
US6203803B1 (en) | 1994-12-14 | 2001-03-20 | Societe L'oreal S.A. | Use of a substance P antagonist in a cosmetic composition, and the composition thus obtained |
FR2719474B1 (en) * | 1994-05-05 | 1996-05-31 | Oreal | Use of a substance P antagonist in a cosmetic composition and composition obtained. |
US5554644A (en) * | 1994-06-08 | 1996-09-10 | Warner-Lambert Company | Tachykinin (NK2) antagonists |
GB9415997D0 (en) * | 1994-08-08 | 1994-09-28 | Merck Sharp & Dohme | Therapeutic agents |
FR2728265A1 (en) * | 1994-12-19 | 1996-06-21 | Oreal | USE OF A SUBSTANCE P ANTAGONIST IN A PHARMACEUTICAL COMPOSITION |
FR2728165A1 (en) † | 1994-12-19 | 1996-06-21 | Oreal | USE OF AN ANTAGONIST OF SUBSTANCE P FOR THE TREATMENT OF SKIN REDNESS OF NEUROGENIC ORIGIN |
FR2732598B1 (en) | 1995-04-10 | 1997-05-09 | Oreal | USE OF ALKALINE EARTH METAL SALT FOR THE TREATMENT OF PRURITUS AND EYE OR PALPEBRAL DYSESTHESIA |
EP0737471A3 (en) * | 1995-04-10 | 2000-12-06 | L'oreal | Use of alkaline earth metal salts as TNF-alpha inhibitor in a topical composition and composition obtained therefrom |
FR2737408B1 (en) * | 1995-07-31 | 1997-09-05 | Oreal | USE OF A BRADYKININE ANTAGONIST IN A COSMETIC, PHARMACEUTICAL OR DERMATOLOGICAL COMPOSITION AND COMPOSITION OBTAINED |
FR2738741B1 (en) * | 1995-09-19 | 1997-12-05 | Oreal | COMPOSITION FOR DYEING KERATINIC FIBERS, CONTAINING AN ANTAGONIST OF SUBSTANCE P |
TW458774B (en) | 1995-10-20 | 2001-10-11 | Pfizer | Antiemetic pharmaceutical compositions |
FR2740341B1 (en) * | 1995-10-26 | 1997-12-19 | Oreal | USE OF LANTHANIDE SALT, TIN, ZINC, MANGANESE, YTTRIUM, COBALT, BARIUM, STRONTIUM IN A SKIN COMPOSITION |
FR2740335B1 (en) * | 1995-10-26 | 1997-12-19 | Oreal | USE OF LANTHANIDE, LITHIUM, TIN, ZINC, MANGANESE OR YTTRIUM SALT AS A SUBSTANCE P ANTAGONIST |
AU2898297A (en) * | 1996-05-24 | 1998-01-05 | Novartis Ag | Use of substance p antagonists for treating social phobia |
AU729708B2 (en) * | 1996-12-02 | 2001-02-08 | Merck Sharp & Dohme Limited | Use of NK-1 receptor antagonists for treating severe anxiety disorders |
GB9716463D0 (en) * | 1997-08-04 | 1997-10-08 | Merck Sharp & Dohme | Therapeutic agents |
JP2000103782A (en) * | 1998-07-31 | 2000-04-11 | Kyorin Pharmaceut Co Ltd | Cyclic amine derivative and its production |
CA2369695A1 (en) * | 1999-04-09 | 2000-10-19 | Manabu Itoh | Agent for treating neuropathic pain |
US7163949B1 (en) | 1999-11-03 | 2007-01-16 | Amr Technology, Inc. | 4-phenyl substituted tetrahydroisoquinolines and use thereof |
EP1246806B1 (en) | 1999-11-03 | 2008-02-27 | AMR Technology, Inc. | Arly- and heteroaryl-substituted tetrahydroisoquinolines and use thereof to block reuptake of norepinephrine, dopamine and serotonin |
AU7334901A (en) | 2000-07-11 | 2002-01-21 | Du Pont Pharm Co | Novel 4-phenyl substituted tetrahydroisoquinolines and therapeutic use thereof |
ES2382814T3 (en) | 2005-05-17 | 2012-06-13 | Merck Sharp & Dohme Ltd. | Cis-4 - [(4-chlorophenyl) sulfonyl] -4- (2,5-difluorophenyl) cyclohexanopropanoic acid for cancer treatment |
US7956050B2 (en) | 2005-07-15 | 2011-06-07 | Albany Molecular Research, Inc. | Aryl- and heteroaryl-substituted tetrahydrobenzazepines and use thereof to block reuptake of norepinephrine, dopamine, and serotonin |
JP4879988B2 (en) | 2005-09-29 | 2012-02-22 | メルク・シャープ・エンド・ドーム・コーポレイション | Acylated spiropiperidine derivatives as melanocortin-4 receptor modulators |
GB0603041D0 (en) | 2006-02-15 | 2006-03-29 | Angeletti P Ist Richerche Bio | Therapeutic compounds |
CA2770486C (en) | 2006-09-22 | 2014-07-15 | Merck Sharp & Dohme Corp. | Use of platencin and platensimycin as fatty acid synthesis inhibitors to treat obesity, diabetes and cancer |
US20110218176A1 (en) | 2006-11-01 | 2011-09-08 | Barbara Brooke Jennings-Spring | Compounds, methods, and treatments for abnormal signaling pathways for prenatal and postnatal development |
PL2109608T3 (en) | 2007-01-10 | 2011-08-31 | Msd Italia Srl | Amide substituted indazoles as poly(adp-ribose)polymerase (parp) inhibitors |
AU2008233662B2 (en) | 2007-04-02 | 2012-08-23 | Msd K.K. | Indoledione derivative |
JP5501227B2 (en) | 2007-06-27 | 2014-05-21 | メルク・シャープ・アンド・ドーム・コーポレーション | 4-Carboxybenzylamino derivatives as histone deacetylase inhibitors |
JP2011515343A (en) | 2008-03-03 | 2011-05-19 | タイガー ファーマテック | Tyrosine kinase inhibitor |
UA105182C2 (en) | 2008-07-03 | 2014-04-25 | Ньюрексон, Інк. | Benzoxazines, benzothiazines, and related compounds having nos inhibitory activity |
WO2010114780A1 (en) | 2009-04-01 | 2010-10-07 | Merck Sharp & Dohme Corp. | Inhibitors of akt activity |
DK2429296T3 (en) | 2009-05-12 | 2018-03-12 | Albany Molecular Res Inc | 7 - ([1,2,4,] TRIAZOLO [1,5, -A] PYRIDIN-6-YL) -4- (3,4-DICHLORPHENYL) -1,2,3,4- TETRAHYDROISOQUINOLINE AND USE thereof |
US8859776B2 (en) | 2009-10-14 | 2014-10-14 | Merck Sharp & Dohme Corp. | Substituted piperidines that increase p53 activity and the uses thereof |
EP2584903B1 (en) | 2010-06-24 | 2018-10-24 | Merck Sharp & Dohme Corp. | Novel heterocyclic compounds as erk inhibitors |
JP6043285B2 (en) | 2010-08-02 | 2016-12-14 | サーナ・セラピューティクス・インコーポレイテッドSirna Therapeutics,Inc. | RNA interference-mediated inhibition of catenin (cadherin-binding protein) β1 (CTNNB1) gene expression using small interfering nucleic acids (siNA) |
RU2624045C2 (en) | 2010-08-17 | 2017-06-30 | Сирна Терапьютикс,Инк | RNA INTERFERENCE MEDIATED INHIBITION OF HEPATITIS B VIRUS (HBV) GENE EXPRESSION USING SHORT INTERFERING NUCLEIC ACID (siNA) |
US8883801B2 (en) | 2010-08-23 | 2014-11-11 | Merck Sharp & Dohme Corp. | Substituted pyrazolo[1,5-a]pyrimidines as mTOR inhibitors |
EP2613782B1 (en) | 2010-09-01 | 2016-11-02 | Merck Sharp & Dohme Corp. | Indazole derivatives useful as erk inhibitors |
US9242981B2 (en) | 2010-09-16 | 2016-01-26 | Merck Sharp & Dohme Corp. | Fused pyrazole derivatives as novel ERK inhibitors |
EP2632472B1 (en) | 2010-10-29 | 2017-12-13 | Sirna Therapeutics, Inc. | Rna interference mediated inhibition of gene expression using short interfering nucleic acids (sina) |
WO2012087772A1 (en) | 2010-12-21 | 2012-06-28 | Schering Corporation | Indazole derivatives useful as erk inhibitors |
CN103732592A (en) | 2011-04-21 | 2014-04-16 | 默沙东公司 | Insulin-like growth factor-1 receptor inhibitors |
US9023865B2 (en) | 2011-10-27 | 2015-05-05 | Merck Sharp & Dohme Corp. | Compounds that are ERK inhibitors |
US20150299696A1 (en) | 2012-05-02 | 2015-10-22 | Sirna Therapeutics, Inc. | SHORT INTERFERING NUCLEIC ACID (siNA) COMPOSITIONS |
CA2882950A1 (en) | 2012-09-28 | 2014-04-03 | Merck Sharp & Dohme Corp. | Novel compounds that are erk inhibitors |
RU2660349C2 (en) | 2012-11-28 | 2018-07-05 | Мерк Шарп И Доум Корп. | Compositions and methods for treatment of malignant tumour |
WO2014100065A1 (en) | 2012-12-20 | 2014-06-26 | Merck Sharp & Dohme Corp. | Substituted imidazopyridines as hdm2 inhibitors |
WO2014120748A1 (en) | 2013-01-30 | 2014-08-07 | Merck Sharp & Dohme Corp. | 2,6,7,8 substituted purines as hdm2 inhibitors |
EP3041938A1 (en) | 2013-09-03 | 2016-07-13 | Moderna Therapeutics, Inc. | Circular polynucleotides |
EP3706742B1 (en) | 2017-11-08 | 2023-03-15 | Merck Sharp & Dohme LLC | Prmt5 inhibitors |
US20210309688A1 (en) | 2018-08-07 | 2021-10-07 | Merck Sharp & Dohme Corp. | Prmt5 inhibitors |
WO2020033282A1 (en) | 2018-08-07 | 2020-02-13 | Merck Sharp & Dohme Corp. | Prmt5 inhibitors |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0007258A1 (en) * | 1978-06-29 | 1980-01-23 | Pharmuka Laboratoires | Indole derivatives and their use as anxiolytics |
EP0428434A2 (en) * | 1989-11-06 | 1991-05-22 | Sanofi | Compounds of aromatic amines and their enantiomers, process for their preparation and pharmaceutical compositions containing them |
EP0436334A2 (en) * | 1990-01-04 | 1991-07-10 | Pfizer Inc. | 3-Aminopiperidine derivatives and related nitrogen containing heterocycles |
EP0474561A1 (en) * | 1990-09-05 | 1992-03-11 | Sanofi | Arylalkylamines, process for their preparation and pharmaceutical compositions containing them |
EP0512901A1 (en) * | 1991-05-03 | 1992-11-11 | Sanofi | Aminated polycyclic compounds and their enantiomers, process for their preparation and pharmaceutical compositions containing them |
-
1992
- 1992-01-21 GB GB929201179A patent/GB9201179D0/en active Pending
-
1993
- 1993-01-15 AU AU33513/93A patent/AU3351393A/en not_active Abandoned
- 1993-01-15 WO PCT/EP1993/000101 patent/WO1993014084A2/en active Application Filing
- 1993-01-20 IL IL104445A patent/IL104445A0/en unknown
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0007258A1 (en) * | 1978-06-29 | 1980-01-23 | Pharmuka Laboratoires | Indole derivatives and their use as anxiolytics |
EP0428434A2 (en) * | 1989-11-06 | 1991-05-22 | Sanofi | Compounds of aromatic amines and their enantiomers, process for their preparation and pharmaceutical compositions containing them |
EP0436334A2 (en) * | 1990-01-04 | 1991-07-10 | Pfizer Inc. | 3-Aminopiperidine derivatives and related nitrogen containing heterocycles |
EP0474561A1 (en) * | 1990-09-05 | 1992-03-11 | Sanofi | Arylalkylamines, process for their preparation and pharmaceutical compositions containing them |
EP0512901A1 (en) * | 1991-05-03 | 1992-11-11 | Sanofi | Aminated polycyclic compounds and their enantiomers, process for their preparation and pharmaceutical compositions containing them |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US9499531B2 (en) | 2004-07-15 | 2016-11-22 | Albany Molecular Research, Inc. | Aryl- and heteroaryl-substituted tetrahydroisoquinolines and use thereof to block reuptake of norepinephrine, dopamine, and serotonin |
US9156812B2 (en) | 2008-06-04 | 2015-10-13 | Bristol-Myers Squibb Company | Crystalline form of 6-[(4S)-2-methyl-4-(2-naphthyl)-1,2,3,4-tetrahydroisoquinolin-7-yl]pyridazin-3-amine |
US9498476B2 (en) | 2008-06-04 | 2016-11-22 | Albany Molecular Research, Inc. | Crystalline form of 6-[(4S)-2-methyl-4-(2-naphthyl)-1,2,3,4-tetrahydroisoquinolin-7-yl]pyridazin-3-amine |
US9034899B2 (en) | 2009-05-12 | 2015-05-19 | Albany Molecular Research, Inc. | Aryl, heteroaryl, and heterocycle substituted tetrahydroisoquinolines and use thereof |
US9173879B2 (en) | 2009-05-12 | 2015-11-03 | Bristol-Myers Squibb Company | Crystalline forms of (S)-7-([1,2,4]triazolo[1,5-a ]pyridin-6-yl)-4-(3,4-dichlorophenyl)-1,2,3,4-tetrahydroisoquinoline and use thereof |
Also Published As
Publication number | Publication date |
---|---|
GB9201179D0 (en) | 1992-03-11 |
AU3351393A (en) | 1993-08-03 |
WO1993014084A2 (en) | 1993-07-22 |
IL104445A0 (en) | 1993-05-13 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
WO1993014084A3 (en) | Piperidine derivatives | |
IL103214A0 (en) | Pharmaceutical compositions containing tachykinin antagonists for the treatment of emesis and certain novel tachykinin antagonists | |
EP0389282A3 (en) | Xanthinederivatives, process for their preparation and their pharmaceutical use | |
HU9303145D0 (en) | Process for producing of fibrinogen receptor antagonist compounds and pharmaceutical compositions containing them as medical agent | |
ATE139233T1 (en) | ANNELATED THIOPHENE DERIVATIVES, THEIR PREPARATION AND USE | |
SE0104334D0 (en) | Therapeutic agents | |
ES8609309A1 (en) | 3-Imidazolylmethyl-1,2,3,9-tetrahydro-4H-carbazol-4-one derivatives | |
PH23607A (en) | Amide derivatives and pharmaceutical composition containing said compounds | |
IL87658A0 (en) | Lactam derivatives,their preparation and pharmaceutical compositions containing them | |
KR850000462A (en) | [[Bis (aryl) methylene] -1-piperidinyl] alkyl-pyrimidinone | |
HUP0204162A2 (en) | Spiro(2h-1-benzopyran-2,4'-piperidine) derivatives as glycine transport inhibitors and pharmaceutical compositions containing them | |
ES8207180A1 (en) | Thienopyridinone derivatives, process for their preparation and their therapeutical use. | |
NO972887L (en) | Piperidinedacetic acid derivatives useful as fibrinogen antagonist agent | |
NZ515407A (en) | 4-Phenyl-pyrimidine derivatives | |
IL85768A0 (en) | Benzoxazine derivatives,their preparation and pharmaceutical compositions containing them | |
ES2019554A6 (en) | 2-substituted N,N'-ditrimethoxybenzoyl piperazines and therapeutic compositions containing them | |
GB8701494D0 (en) | Chemical compounds | |
KR950704322A (en) | Spirofuranone Derivatives and Their Use in the Treatment of Neurodegenerative Disorders | |
EP0461264A4 (en) | Ethynylphenyl derivative, production thereof, and remedy for diseases of circulatory organs containing the same as active ingredient | |
NO308304B1 (en) | Novel 5H-thiazol [3,2-a] pyrimidin-5-one derivatives, their use in the preparation of pharmaceutical compositions, pharmaceutical compositions containing the derivatives, and a preparation for the treatment of psychosis, schizophrenia and anxiety | |
ES2058761T3 (en) | PROCESS FOR THE PREPARATION OF DIBENZODIOXAZECINE AND DIBENZODIOXAAZACICLOUNDECINE DERIVATIVES. |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
AK | Designated states |
Kind code of ref document: A2 Designated state(s): AT AU BB BG BR CA CH CZ DE DK ES FI GB HU JP KP KR LK LU MG MN MW NL NO NZ PL PT RO RU SD SE SK UA US |
|
AL | Designated countries for regional patents |
Kind code of ref document: A2 Designated state(s): AT BE CH DE DK ES FR GB GR IE IT LU MC NL PT SE BF BJ CF CG CI CM GA GN ML MR SN TD TG |
|
AK | Designated states |
Kind code of ref document: A3 Designated state(s): AT AU BB BG BR CA CH CZ DE DK ES FI GB HU JP KP KR LK LU MG MN MW NL NO NZ PL PT RO RU SD SE SK UA US |
|
AL | Designated countries for regional patents |
Kind code of ref document: A3 Designated state(s): AT BE CH DE DK ES FR GB GR IE IT LU MC NL PT SE BF BJ CF CG CI CM GA GN ML MR SN TD TG |
|
122 | Ep: pct application non-entry in european phase | ||
REG | Reference to national code |
Ref country code: DE Ref legal event code: 8642 |
|
NENP | Non-entry into the national phase |
Ref country code: CA |