AR080375A1 - Procedimiento para la preparacion de 2-(cicloheximetil)-n-{2-[(2s)-1-metilpirrolidin-2-il] etil}-1,2,3,4-tetrahidroisoquinolina- 7-sulfonamida - Google Patents
Procedimiento para la preparacion de 2-(cicloheximetil)-n-{2-[(2s)-1-metilpirrolidin-2-il] etil}-1,2,3,4-tetrahidroisoquinolina- 7-sulfonamidaInfo
- Publication number
- AR080375A1 AR080375A1 ARP110100673A ARP110100673A AR080375A1 AR 080375 A1 AR080375 A1 AR 080375A1 AR P110100673 A ARP110100673 A AR P110100673A AR P110100673 A ARP110100673 A AR P110100673A AR 080375 A1 AR080375 A1 AR 080375A1
- Authority
- AR
- Argentina
- Prior art keywords
- tetrahydroisoquinoline
- cyclohexylmethyl
- salt
- sulfonamide
- methylpyrrolidin
- Prior art date
Links
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
- C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
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- 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
- A61K31/472—Non-condensed isoquinolines, e.g. papaverine
- A61K31/4725—Non-condensed isoquinolines, e.g. papaverine containing further heterocyclic rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/04—Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/08—Antiepileptics; Anticonvulsants
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/14—Drugs for disorders of the nervous system for treating abnormal movements, e.g. chorea, dyskinesia
- A61P25/16—Anti-Parkinson drugs
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/18—Antipsychotics, i.e. neuroleptics; Drugs for mania or schizophrenia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/22—Anxiolytics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/24—Antidepressants
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
-
- 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
- A61P3/04—Anorexiants; Antiobesity agents
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P5/00—Drugs for disorders of the endocrine system
- A61P5/18—Drugs for disorders of the endocrine system of the parathyroid hormones
- A61P5/20—Drugs for disorders of the endocrine system of the parathyroid hormones for decreasing, blocking or antagonising the activity of PTH
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- 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
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
- C07C51/41—Preparation of salts of carboxylic acids
- C07C51/412—Preparation of salts of carboxylic acids by conversion of the acids, their salts, esters or anhydrides with the same carboxylic acid part
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D217/00—Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems
- C07D217/02—Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems with only hydrogen atoms or radicals containing only carbon and hydrogen atoms, directly attached to carbon atoms of the nitrogen-containing ring; Alkylene-bis-isoquinolines
- C07D217/04—Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems with only hydrogen atoms or radicals containing only carbon and hydrogen atoms, directly attached to carbon atoms of the nitrogen-containing ring; Alkylene-bis-isoquinolines with hydrocarbon or substituted hydrocarbon radicals attached to the ring nitrogen atom
-
- 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
- C07D403/12—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 chain containing hetero atoms as chain links
Abstract
Reivindicacion 1: Un procedimiento para preparar 2-(ciclohexilmetil)-N-{2-[(2S)-1-metilpirrolidin-2-il]etil}-1,2,3,4-tetrahidroisoquinolina-7-sulfonamida, o una sal farmacéuticamente aceptable de la misma o un solvato o hidrato de una sal farmacéuticamente aceptable que comprende: a) la aminacion reductora de 1,2,3,4-tetrahidroisoquinolina, o una de sus sales, con ciclohexanocarboxaldehído para dar 2-ciclohexilmetil-1,2,3,4-tetrahidroisoquinolina, o una de sus sales; b) hacer reaccionar 2-ciclohexilmetil-1,2,3.4-tetrahidroisoquinolina, o una de sus sales, con un exceso de ácido clorosulfonico para dar la sal HX del cloruro de 2-ciclohexilmetil-1,2,3,4-tetrahidroisoquinolina-7-sulfonilo, y opcionalmente recristalizar la sal HX del cloruro de 2-ciclohexilmetil-1,2,3,4-tetrahidroisoquinolina-7-sulfonilo; c) acoplar la sal HX del cloruro de 2-ciclohexilmetil-1,2,3,4-tetrahidroisoquinolina-7-sulfonilo con (-)-2-(2-aminoetil)-1-metilpirrolidina para formar 2-(ciclohexilmetil)-N-{2-[(2S)-1-metilpirrolidin-2-il]etil}-1,2,3,4-tetrahidroisoquinolina-7-sulfonamida; d) hacer reaccionar opcionalmente 2-(ciclohexilmetil)-N-{2-[(2S)-1-metilpirrolidin-2-il]etil}-1,2,3,4-tetrahidroisoquinolina-7-sulfonamida con una cantidad estequiométrica o un exceso de un ácido formador de sal en un disolvente para formar una sal o un hidrato o solvato de la misma; y e) recristalizar opcionalmente el producto de la etapa d).
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US31106910P | 2010-03-05 | 2010-03-05 | |
FR1059750 | 2010-11-25 |
Publications (1)
Publication Number | Publication Date |
---|---|
AR080375A1 true AR080375A1 (es) | 2012-04-04 |
Family
ID=44012569
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ARP110100672A AR080374A1 (es) | 2010-03-05 | 2011-03-03 | Procedimiento para la preparcion de 2-(ciclohexilmetil)-n-(2-((2s)-1-metilpirrolidin-2-il) etil)- 1,2,3,4-tetrahidroisoquinolin-7- sulfonamida |
ARP110100673A AR080375A1 (es) | 2010-03-05 | 2011-03-03 | Procedimiento para la preparacion de 2-(cicloheximetil)-n-{2-[(2s)-1-metilpirrolidin-2-il] etil}-1,2,3,4-tetrahidroisoquinolina- 7-sulfonamida |
Family Applications Before (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ARP110100672A AR080374A1 (es) | 2010-03-05 | 2011-03-03 | Procedimiento para la preparcion de 2-(ciclohexilmetil)-n-(2-((2s)-1-metilpirrolidin-2-il) etil)- 1,2,3,4-tetrahidroisoquinolin-7- sulfonamida |
Country Status (27)
Country | Link |
---|---|
US (2) | US8748615B2 (es) |
EP (2) | EP2542530A2 (es) |
JP (2) | JP5927126B2 (es) |
KR (2) | KR101783679B1 (es) |
CN (2) | CN103221394A (es) |
AR (2) | AR080374A1 (es) |
AU (2) | AU2011222588B2 (es) |
BR (2) | BR112012022234A2 (es) |
CA (2) | CA2787427C (es) |
CL (2) | CL2012002452A1 (es) |
CO (2) | CO6630099A2 (es) |
CR (1) | CR20120467A (es) |
DO (1) | DOP2012000228A (es) |
EC (1) | ECSP12012207A (es) |
GT (1) | GT201200228A (es) |
IL (2) | IL221339A0 (es) |
MA (2) | MA34142B1 (es) |
MX (2) | MX2012008422A (es) |
NZ (2) | NZ602009A (es) |
PE (1) | PE20130007A1 (es) |
RU (2) | RU2012142310A (es) |
SG (2) | SG183256A1 (es) |
TN (1) | TN2012000361A1 (es) |
TW (2) | TW201144284A (es) |
UY (2) | UY33263A (es) |
WO (2) | WO2011109675A2 (es) |
ZA (1) | ZA201205311B (es) |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
AR080374A1 (es) | 2010-03-05 | 2012-04-04 | Sanofi Aventis | Procedimiento para la preparcion de 2-(ciclohexilmetil)-n-(2-((2s)-1-metilpirrolidin-2-il) etil)- 1,2,3,4-tetrahidroisoquinolin-7- sulfonamida |
CN102816101A (zh) * | 2012-08-21 | 2012-12-12 | 江苏恒祥化工有限责任公司 | 一种(s)-n-甲基-2氯乙基吡咯烷的合成方法 |
WO2015032966A1 (en) * | 2013-09-09 | 2015-03-12 | Sanofi | An h3 receptor antagonist combined with a cholinesterase inhibitor for use in the treatment of alzheimer's disease |
JP2020536100A (ja) * | 2017-10-04 | 2020-12-10 | セルジーン コーポレイション | シス−4−[2−{[(3s,4r)−3−フルオロキサン−4−イル]アミノ}−8−(2,4,6−トリクロロアニリノ)−9h−プリン−9−イル]−1−メチルシクロヘキサン−1−カルボキサミドの製造プロセス |
Family Cites Families (49)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4228170A (en) | 1979-08-30 | 1980-10-14 | Smithkline Corporation | 7- and/or 8-Sulfur substituted 1,2,3,4-tetrahydroisoquinoline compounds |
US4315935A (en) * | 1980-04-14 | 1982-02-16 | Smithkline Corporation | N,N'-Bis[substituted-1,2,3,4-tetrahydroisoquinolinolyl]disulfonylimides and antiallergic compositions and method of use |
GB8717374D0 (en) | 1987-07-22 | 1987-08-26 | Smith Kline French Lab | Pharmaceutically active compounds |
US4857301A (en) | 1987-09-25 | 1989-08-15 | Schering Corporation | Sulfonamide compounds, compositions and method of use |
EP0702671A4 (en) | 1993-06-09 | 1996-06-19 | Smithkline Beecham Corp | BICYCLIC FIBRINOGEN ANTAGONISTS |
GB9322976D0 (en) | 1993-11-08 | 1994-01-05 | Pfizer Ltd | Therapeutic agents |
GB9709303D0 (en) * | 1997-05-09 | 1997-06-25 | Smithkline Beecham Plc | Compounds |
IL138899A0 (en) | 1998-04-10 | 2001-11-25 | Japan Tobacco Inc | Amidene derivatives and pharmaceutical compositions containing the same |
GB9816984D0 (en) | 1998-08-05 | 1998-09-30 | Smithkline Beecham Plc | Novel compounds |
WO2000023437A1 (fr) | 1998-10-16 | 2000-04-27 | Takeda Chemical Industries, Ltd. | Composes azotes hererocycliques condenses; procede de fabrication et agents les renfermant |
SK13532001A3 (sk) | 1999-04-01 | 2003-02-04 | Pfizer Products Inc. | Aminopiridíny ako inhibítory sorbitoldehydrogenázy |
GB9912410D0 (en) | 1999-05-28 | 1999-07-28 | Pfizer Ltd | Compounds useful in therapy |
AR025884A1 (es) | 1999-10-01 | 2002-12-18 | Takeda Pharmaceutical | Compuestos de amina ciclica, su produccion y su uso |
CN1215059C (zh) | 1999-12-03 | 2005-08-17 | 京都药品工业株式会社 | 新的杂环化合物及其盐和它们的医药用途 |
FR2804429B1 (fr) | 2000-01-31 | 2003-05-09 | Adir | Nouveaux derives de 4-sulfonamides piperidine, leur procede de preparation et les compositions pharmaceutiques qui les contiennent |
FR2807434B1 (fr) | 2000-04-05 | 2002-10-18 | Hoechst Marion Roussel Inc | Nouveaux derives de la 1,2,3,4-tetrahydroisoquinoleine, leur procede de preparation et leur application comme fongicides |
EP1326830A1 (en) | 2000-10-20 | 2003-07-16 | Biovitrum Ab | 2-, 3-, 4-, or 5-substituted-n1-(benzensulfonyl)indoles and their use in therapy |
US20040039044A1 (en) * | 2000-10-30 | 2004-02-26 | Yuanjin Rui | Aminoalkylpyrrolidine serotonin receptor ligands and compositions, their pharmaceutical uses, and methods for their synthesis |
AU2002254114A1 (en) | 2001-03-23 | 2002-10-08 | Eli Lilly And Company | Non-imidazole aryl alkylamines compounds as histamine h3 receptor antagonists, preparation and therapeutic uses |
EP1408030B1 (en) * | 2001-06-18 | 2006-01-04 | Maruha Corporation | Novel aliphatic compound, method of synthesis, and method of utilization |
CA2456096A1 (en) | 2001-08-01 | 2003-02-13 | Mochida Pharmaceutical Co., Ltd. | Novel amine derivative having human .beta.-tryptase inhibitory activity and medecine containing the same |
US6677349B1 (en) | 2001-12-21 | 2004-01-13 | 3M Innovative Properties Company | Sulfonamide and sulfamide substituted imidazoquinolines |
US20050154230A1 (en) | 2001-12-26 | 2005-07-14 | Bayer Healthcare Ag | Urea derivatives |
US6867224B2 (en) | 2002-03-07 | 2005-03-15 | Warner-Lambert Company | Compounds that modulate PPAR activity and methods of preparation |
AU2004232939A1 (en) | 2003-04-17 | 2004-11-04 | Merck Sharp & Dohme Corp. | Heterocyclic cyclopentyl tetrahydroisoquinoline and tetrahydropyridopyridine modulators of chemokine receptor activity |
FR2857695B1 (fr) | 2003-07-15 | 2007-04-20 | Saint Gobain Ct Recherches | Bloc pour la filtration de particules contenues dans les gaz d'echappement d'un moteur a combustion interne |
EP1701724A4 (en) | 2004-01-02 | 2007-11-14 | Merck & Co Inc | CYCLOPENTYL AMIDE MODULATORS OF ALKYLAMINO, ARYLAMINO AND SULFONAMIDO OF CHEMOKINE RECEPTOR ACTIVITY |
AU2005206791A1 (en) | 2004-01-20 | 2005-08-04 | Merck Sharp & Dohme Corp. | 2,6-disubstituted piperidines as modulators of chemokine receptor activity |
WO2005110409A2 (en) | 2004-04-26 | 2005-11-24 | Merck & Co., Inc. | Tetrahydropyranyl cyclopentyl 1-substituted and 1,1-disubstituted tetrahydroisoquinoline modulators of chemokine receptor activity |
US7557124B2 (en) | 2004-04-26 | 2009-07-07 | Merck & Co., Inc. | Tetrahydropyranyl cyclopentyl tetrahydropyridopyridine modulators of chemokine receptor activity |
GEP20084519B (en) | 2004-05-11 | 2008-10-27 | Incyte Corp | 3-(4-heteroarylcyclo-hexylamino) cyclopenta-necarboxamides as modulators of chemokine receptors |
FR2870846B1 (fr) | 2004-05-25 | 2006-08-04 | Sanofi Synthelabo | Derives de tetrahydroisoquinolylsulfonamides, leur preparation et leur utilisation en therapeutique |
WO2005123089A2 (en) | 2004-06-10 | 2005-12-29 | Kalypsys, Inc. | Multicyclic sulfonamide compounds as inhibitors of histone deacetylase for the treatment of disease |
EP1630158A1 (en) | 2004-08-18 | 2006-03-01 | Laboratorios Del Dr. Esteve, S.A. | 5-HT7 receptor antagonists |
ES2257168B1 (es) | 2004-08-18 | 2007-06-01 | Laboratorios Del Dr Esteve, S.A. | Ligandos del receptor 5-ht7. |
ES2442678T3 (es) | 2004-08-28 | 2014-02-12 | Astrazeneca Ab | Derivados de pirimidín sulfonamidas como moduladores del receptor de quimioquina |
SE0403086D0 (sv) | 2004-12-17 | 2004-12-17 | Astrazeneca Ab | Compounds |
EP1828185B1 (en) | 2004-12-21 | 2009-05-06 | SmithKline Beecham Corporation | 2-pyrimidinyl pyrazolopyridine erbb kinase inhibitors |
US20090264425A1 (en) | 2004-12-22 | 2009-10-22 | Pfizer Limited | Chemical compounds |
DE602006010175D1 (de) | 2005-01-26 | 2009-12-17 | Hoffmann La Roche | Phenylmethanonderivate und ihre verwendung als glycin-transporter-1-hemmer |
DE102005015040A1 (de) | 2005-03-31 | 2006-10-05 | Sanofi-Aventis Deutschland Gmbh | Substituierte Tetrahydroisochinoline als MMP-Inhibitoren, Verfahren zu ihrer Herstellung und ihre Verwendung als Medikament |
AR053845A1 (es) | 2005-04-15 | 2007-05-23 | Tibotec Pharm Ltd | 5-tiazolilmetil[(1s,2r)-3-[[(2-amino-6-benzoxazolil)sulfonil)](2-metilpropil)amino]-2-hidroxi-1-(fenilmetil)propil]carbamato como mejorador de farmacos metabolizados por el citocromo p450 |
RU2007145434A (ru) | 2005-05-10 | 2009-06-20 | Вертекс Фармасьютикалз Инкорпорейтед (Us) | Бициклические производные в качестве модуляторов ионных каналов |
EP1911747A1 (en) | 2006-10-11 | 2008-04-16 | Laboratorios del Dr. Esteve S.A. | Sulfonamide substituted pyrazoline compounds, their preparation and use as CB1 modulators |
WO2008136378A1 (ja) | 2007-04-27 | 2008-11-13 | Toyama Chemical Co., Ltd. | 新規なスルホンアミド誘導体またはその塩 |
CN102036952A (zh) | 2008-04-16 | 2011-04-27 | 比奥里波克斯公司 | 用作药物的双芳基化合物 |
WO2010127272A2 (en) | 2009-04-30 | 2010-11-04 | Concert Pharmaceuticals, Inc. | Hydroxyethylamino sulfonamide derivatives |
EP2445899B1 (en) | 2009-06-26 | 2016-05-11 | Sanofi | Novel fumarate salts of a histamine h3 receptor antagonist |
AR080374A1 (es) | 2010-03-05 | 2012-04-04 | Sanofi Aventis | Procedimiento para la preparcion de 2-(ciclohexilmetil)-n-(2-((2s)-1-metilpirrolidin-2-il) etil)- 1,2,3,4-tetrahidroisoquinolin-7- sulfonamida |
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2011
- 2011-03-03 AR ARP110100672A patent/AR080374A1/es unknown
- 2011-03-03 AR ARP110100673A patent/AR080375A1/es unknown
- 2011-03-04 RU RU2012142310/04A patent/RU2012142310A/ru not_active Application Discontinuation
- 2011-03-04 JP JP2012556254A patent/JP5927126B2/ja not_active Expired - Fee Related
- 2011-03-04 CA CA2787427A patent/CA2787427C/en not_active Expired - Fee Related
- 2011-03-04 BR BR112012022234A patent/BR112012022234A2/pt not_active Application Discontinuation
- 2011-03-04 KR KR1020127020498A patent/KR101783679B1/ko active IP Right Grant
- 2011-03-04 CN CN2011800123082A patent/CN103221394A/zh active Pending
- 2011-03-04 NZ NZ602009A patent/NZ602009A/en not_active IP Right Cessation
- 2011-03-04 PE PE2012001391A patent/PE20130007A1/es not_active Application Discontinuation
- 2011-03-04 TW TW100107248A patent/TW201144284A/zh unknown
- 2011-03-04 CN CN201180012335XA patent/CN103068815A/zh active Pending
- 2011-03-04 AU AU2011222588A patent/AU2011222588B2/en not_active Ceased
- 2011-03-04 MA MA35286A patent/MA34142B1/fr unknown
- 2011-03-04 MX MX2012008422A patent/MX2012008422A/es active IP Right Grant
- 2011-03-04 JP JP2012556252A patent/JP2013521308A/ja not_active Ceased
- 2011-03-04 AU AU2011223560A patent/AU2011223560A1/en not_active Abandoned
- 2011-03-04 SG SG2012059242A patent/SG183256A1/en unknown
- 2011-03-04 BR BR112012022356A patent/BR112012022356A2/pt not_active IP Right Cessation
- 2011-03-04 WO PCT/US2011/027118 patent/WO2011109675A2/en active Application Filing
- 2011-03-04 UY UY0001033263A patent/UY33263A/es not_active Application Discontinuation
- 2011-03-04 RU RU2012142338/04A patent/RU2012142338A/ru not_active Application Discontinuation
- 2011-03-04 UY UY0001033262A patent/UY33262A/es not_active Application Discontinuation
- 2011-03-04 KR KR1020127025953A patent/KR20130047685A/ko not_active Application Discontinuation
- 2011-03-04 NZ NZ601498A patent/NZ601498A/en not_active IP Right Cessation
- 2011-03-04 MA MA35288A patent/MA34144B1/fr unknown
- 2011-03-04 CA CA2789669A patent/CA2789669A1/en not_active Abandoned
- 2011-03-04 TW TW100107250A patent/TW201144285A/zh unknown
- 2011-03-04 EP EP11708373A patent/EP2542530A2/en not_active Withdrawn
- 2011-03-04 WO PCT/US2011/027131 patent/WO2011109680A2/en active Application Filing
- 2011-03-04 MX MX2012009413A patent/MX2012009413A/es active IP Right Grant
- 2011-03-04 EP EP11708374.1A patent/EP2556064B1/en active Active
- 2011-03-04 SG SG2012052809A patent/SG182576A1/en unknown
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2012
- 2012-07-17 TN TNP2012000361A patent/TN2012000361A1/en unknown
- 2012-07-17 ZA ZA2012/05311A patent/ZA201205311B/en unknown
- 2012-07-19 US US13/553,455 patent/US8748615B2/en not_active Expired - Fee Related
- 2012-07-20 GT GT201200228A patent/GT201200228A/es unknown
- 2012-08-07 IL IL221339A patent/IL221339A0/en unknown
- 2012-08-07 IL IL221341A patent/IL221341A/en not_active IP Right Cessation
- 2012-08-21 DO DO2012000228A patent/DOP2012000228A/es unknown
- 2012-08-31 US US13/600,975 patent/US8779145B2/en not_active Expired - Fee Related
- 2012-09-04 CL CL2012002452A patent/CL2012002452A1/es unknown
- 2012-09-04 CL CL2012002451A patent/CL2012002451A1/es unknown
- 2012-09-13 CR CR20120467A patent/CR20120467A/es unknown
- 2012-10-02 EC ECSP12012207 patent/ECSP12012207A/es unknown
- 2012-10-04 CO CO12174787A patent/CO6630099A2/es not_active Application Discontinuation
- 2012-10-04 CO CO12174778A patent/CO6630129A2/es not_active Application Discontinuation
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