EA200971019A1 - METHODS OF OBTAINING (R) -2-METHILPYRROLIDINE AND (S) -2-METHILPYRROLIDINE AND THEIR SALTS OF WINE ACID - Google Patents
METHODS OF OBTAINING (R) -2-METHILPYRROLIDINE AND (S) -2-METHILPYRROLIDINE AND THEIR SALTS OF WINE ACIDInfo
- Publication number
- EA200971019A1 EA200971019A1 EA200971019A EA200971019A EA200971019A1 EA 200971019 A1 EA200971019 A1 EA 200971019A1 EA 200971019 A EA200971019 A EA 200971019A EA 200971019 A EA200971019 A EA 200971019A EA 200971019 A1 EA200971019 A1 EA 200971019A1
- Authority
- EA
- Eurasian Patent Office
- Prior art keywords
- methilpyrrolidine
- salts
- obtaining
- methods
- wine acid
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D207/04—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom 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
- C07D207/06—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom 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 radicals, containing only hydrogen and carbon atoms, attached to ring carbon atoms
-
- 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
Настоящее изобретение относится к быстрому, безопасному, недорогому и крупномасштабному способу получения (R)- или (S)-2-метилпирролидина из 2-метилпирролина, в котором не требуется выделение синтетических промежуточных соединений.The present invention relates to a fast, safe, inexpensive and large-scale process for the preparation of (R) - or (S) -2-methylpyrrolidine from 2-methylpyrroline, which does not require isolation of synthetic intermediates.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US92735607P | 2007-05-03 | 2007-05-03 | |
PCT/US2008/005702 WO2008137087A1 (en) | 2007-05-03 | 2008-05-02 | Processes for preparing (r)-2-methylpyrrolidine and (s)-2-methylpyrrolidine and tartrate salts thereof |
Publications (2)
Publication Number | Publication Date |
---|---|
EA200971019A1 true EA200971019A1 (en) | 2010-04-30 |
EA019031B1 EA019031B1 (en) | 2013-12-30 |
Family
ID=39688886
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EA200971019A EA019031B1 (en) | 2007-05-03 | 2008-05-02 | Process for preparing 6-{4-[3-((r)-2-methylpyrrolidine-1-yl)propoxy]phenyl}-2h-piridazin-3-one and pharmaceutically acceptable salt thereof |
Country Status (14)
Country | Link |
---|---|
EP (1) | EP2152669A1 (en) |
JP (1) | JP5698887B2 (en) |
KR (1) | KR20100017565A (en) |
CN (1) | CN101679237A (en) |
AU (1) | AU2008248168B2 (en) |
BR (1) | BRPI0810330A2 (en) |
CA (1) | CA2686033A1 (en) |
EA (1) | EA019031B1 (en) |
IL (1) | IL201627A (en) |
MX (1) | MX2009011787A (en) |
NZ (1) | NZ580948A (en) |
UA (1) | UA99913C2 (en) |
WO (1) | WO2008137087A1 (en) |
ZA (1) | ZA200907643B (en) |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
UA95644C2 (en) | 2006-07-25 | 2011-08-25 | Сефалон, Инк. | Pyridizinone derivative, pharmaceutical composition and treatment method |
US8383657B2 (en) | 2007-12-21 | 2013-02-26 | Abbott Laboratories | Thiazolylidine urea and amide derivatives and methods of use thereof |
CA2712885A1 (en) * | 2008-01-30 | 2009-08-06 | Cephalon, Inc. | Substituted pyridazine derivatives which have histamine h3 antagonist activity |
JP6849594B2 (en) * | 2014-12-23 | 2021-03-24 | セファロン、インク. | Method for Preparing Condensed Bicyclic 2,4-diaminopyrimidine Derivatives |
Family Cites Families (20)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE3329974A1 (en) | 1983-08-19 | 1985-02-28 | Bayer Ag, 5090 Leverkusen | MANUFACTURE OF HYDRATED NITRILE RUBBER |
DE3433392A1 (en) | 1984-09-12 | 1986-03-20 | Bayer Ag, 5090 Leverkusen | HYDROGENATION OF UNSATURATED POLYMER WITH NITRILE GROUPS |
FR2714849B1 (en) | 1994-01-13 | 1996-04-05 | Inst Francais Du Petrole | Process for the preparation of a hydrogenation catalyst soluble in the organic liquid phase. |
DE4403479A1 (en) | 1994-02-04 | 1995-08-10 | Basf Ag | Process for the preparation of hydroxylammonium salts |
WO2004024707A2 (en) * | 2002-09-16 | 2004-03-25 | Abbott Laboratories | Process for preparing amine type substituted benzofurans |
US7153889B2 (en) | 2002-11-12 | 2006-12-26 | Abbott Laboratories | Bicyclic-substituted amines as histamine-3 receptor ligands |
US8110519B2 (en) | 2004-03-08 | 2012-02-07 | Japan Science & Technology Agency | Polymer-supported metal cluster composition |
US7145005B2 (en) | 2004-05-12 | 2006-12-05 | Abbott Laboratories | 2-(6-{2-[(2R)-2-Methyl-1-pyrrolidin-1-yl]-ethyl}-2-naphthalen-2-yl)-2H-pyridazin-3-one salts and their preparation |
RU2387638C2 (en) | 2004-06-02 | 2010-04-27 | Ф.Хофманн-ля Рош АГ | Naphthalene derivatives suitable for use as ligands of histamine 3 receptors |
CN101111480A (en) | 2004-12-01 | 2008-01-23 | 万有制药株式会社 | Substituted pyridone derivative |
CA2592353A1 (en) | 2004-12-17 | 2006-06-22 | Janssen Pharmaceutica, N.V. | Tetrahydroisoquinoline compounds for treatment of cns disorders |
CN101107231A (en) | 2005-01-21 | 2008-01-16 | 先灵公司 | Imidazole and benzimidazole derivatives useful as histamine H3 antagonists |
EP1866293A1 (en) | 2005-03-31 | 2007-12-19 | UCB Pharma, S.A. | Compounds comprising an oxazole or thiazole moiety, processes for making them, and their uses |
GB0514812D0 (en) | 2005-07-19 | 2005-08-24 | Glaxo Group Ltd | Compounds |
TW200804274A (en) | 2005-10-27 | 2008-01-16 | Ucb Sa | Compounds comprising a lactam or a lactam derivative moiety, processes for making them, and their uses |
CA2641441A1 (en) | 2006-02-09 | 2007-08-23 | Athersys, Inc. | Pyrazoles for the treatment of obesity and other cns disorders |
WO2007099423A1 (en) | 2006-03-02 | 2007-09-07 | Pfizer Products Inc. | 1-pyrrolidine indane derivatives as histamine-3 receptor antagonists |
WO2007105053A2 (en) | 2006-03-13 | 2007-09-20 | Pfizer Products Inc. | Tetralines antagonists of the h-3 receptor |
WO2008005338A1 (en) | 2006-06-29 | 2008-01-10 | Arena Pharmaceuticals, Inc. | Modulators of the histamine h3-receptor useful for the treatment of disorders related thereto |
UA95644C2 (en) | 2006-07-25 | 2011-08-25 | Сефалон, Инк. | Pyridizinone derivative, pharmaceutical composition and treatment method |
-
2008
- 2008-05-02 EP EP08754205A patent/EP2152669A1/en not_active Withdrawn
- 2008-05-02 EA EA200971019A patent/EA019031B1/en not_active IP Right Cessation
- 2008-05-02 WO PCT/US2008/005702 patent/WO2008137087A1/en active Application Filing
- 2008-05-02 CA CA002686033A patent/CA2686033A1/en not_active Abandoned
- 2008-05-02 AU AU2008248168A patent/AU2008248168B2/en not_active Ceased
- 2008-05-02 CN CN200880021225A patent/CN101679237A/en active Pending
- 2008-05-02 NZ NZ580948A patent/NZ580948A/en not_active IP Right Cessation
- 2008-05-02 MX MX2009011787A patent/MX2009011787A/en active IP Right Grant
- 2008-05-02 JP JP2010507416A patent/JP5698887B2/en not_active Expired - Fee Related
- 2008-05-02 UA UAA200912476A patent/UA99913C2/en unknown
- 2008-05-02 BR BRPI0810330-5A2A patent/BRPI0810330A2/en not_active IP Right Cessation
- 2008-05-02 KR KR1020097025141A patent/KR20100017565A/en not_active Application Discontinuation
-
2009
- 2009-10-19 IL IL201627A patent/IL201627A/en not_active IP Right Cessation
- 2009-10-30 ZA ZA2009/07643A patent/ZA200907643B/en unknown
Also Published As
Publication number | Publication date |
---|---|
JP5698887B2 (en) | 2015-04-08 |
AU2008248168A1 (en) | 2008-11-13 |
EA019031B1 (en) | 2013-12-30 |
ZA200907643B (en) | 2014-03-26 |
KR20100017565A (en) | 2010-02-16 |
EP2152669A1 (en) | 2010-02-17 |
CA2686033A1 (en) | 2008-11-13 |
IL201627A (en) | 2014-06-30 |
BRPI0810330A2 (en) | 2014-10-14 |
UA99913C2 (en) | 2012-10-25 |
JP2010526142A (en) | 2010-07-29 |
NZ580948A (en) | 2011-04-29 |
MX2009011787A (en) | 2009-11-13 |
IL201627A0 (en) | 2010-05-31 |
CN101679237A (en) | 2010-03-24 |
WO2008137087A1 (en) | 2008-11-13 |
AU2008248168B2 (en) | 2013-03-21 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CY1125155T1 (en) | CRYSTAL FORMS OF PROLYL HYDROSYLASE INHIBITOR | |
EA201490474A1 (en) | AMINOHINAZOLINS AS KINAZ INHIBITORS | |
EA202190619A1 (en) | ANTIVIRAL COMPOUNDS | |
CL2012000590A1 (en) | Process to prepare w-transaminase (r) -selective. | |
EA201391274A1 (en) | AMINOHINOLINES AS KINAZ INHIBITORS | |
EA201490596A1 (en) | NEW DYHYDROCHINOLIN-2-IT DERIVATIVES | |
EA201590979A1 (en) | METHODS AND INTERMEDIATE CHEMICAL COMPOUNDS TO OBTAIN PHARMACEUTICAL MEANS | |
CL2009000503A1 (en) | Preparation process of compounds derived from 2-amino-5-cyanobenzoic acid-3-substituted or 1h-pyrazole-5-carboxamide. | |
EA201490567A1 (en) | NEW BICYCLIC DERIVATIVES OF DIHYDROCHINOLIN-2-IT | |
UA111142C2 (en) | FOR THE PREPARATION OF SUBSTITUTED 2-FLUORACRYLIC ACID DERIVATIVES | |
CL2011000296A1 (en) | Process for preparing 4-oxo-octahydro-indole-1-carboxylic acid methyl ester and intermediate compounds used. | |
EA201792538A1 (en) | METHOD OF BIOLOGICAL OBTAINING OF METACRYLIC ACID | |
EA201290550A1 (en) | METHOD OF OBTAINING ACRYLIC AND METHACRYLIC ACID | |
PT2462098E (en) | Process for the preparation of derivatives of 1-(2-halobiphenyl-4-yl)-cyclopropanecarboxylic acid | |
EA201270237A1 (en) | Method of producing 1-benzyl-3-hydroxymethyl-1H-indazole and its derivatives and necessary intermediate compounds containing magnetic | |
EA201391721A1 (en) | METHOD OF OBTAINING POLYMORPHIC FORM I ETHORIKOXIB | |
EA201200820A1 (en) | METHOD OF SYNTHESIS OF INTERMEDIATE PRODUCTS APPLICABLE FOR OBTAINING SUBSTITUTED INDAZOLES AND AZAINDAZOLES | |
EA200971019A1 (en) | METHODS OF OBTAINING (R) -2-METHILPYRROLIDINE AND (S) -2-METHILPYRROLIDINE AND THEIR SALTS OF WINE ACID | |
EA201590116A1 (en) | METHOD OF OBTAINING SUBSTITUTED TRIAZOLOPIRIDINES | |
MY164880A (en) | Process for the preparation of isoxazolyl-methoxy-nicotinic acids | |
EA201270390A1 (en) | 1,2,4-TRIAZIN, WHICH CAN BE USED AS AN ACCELERATOR OF VOLCANIZATION AND A METHOD FOR ITS OBTAINING | |
EA201690467A1 (en) | INDUSTRIAL METHOD FOR SYNTHESIS OF APSETATE PLATESTRATE AND ITS 4'-ACETYL ANALOGUE | |
CR20110208A (en) | PROCESS FOR THE PREPARATION OF BENZONORBORNENOS | |
GB2523674A (en) | Compounds as inhibitor of DNA double-strand break repair, methods and applications thereof | |
NO20084839L (en) | Methods for the preparation of glutamic acid derivatives and meloma products |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
MM4A | Lapse of a eurasian patent due to non-payment of renewal fees within the time limit in the following designated state(s) |
Designated state(s): AM AZ BY KG MD TJ TM |
|
MM4A | Lapse of a eurasian patent due to non-payment of renewal fees within the time limit in the following designated state(s) |
Designated state(s): KZ RU |