AR049446A1 - Preparacion de pregabalina ((s)-(+)-aminometil-5-metilhexanoico) y compuestos relacionados - Google Patents

Preparacion de pregabalina ((s)-(+)-aminometil-5-metilhexanoico) y compuestos relacionados

Info

Publication number
AR049446A1
AR049446A1 ARP050102504A ARP050102504A AR049446A1 AR 049446 A1 AR049446 A1 AR 049446A1 AR P050102504 A ARP050102504 A AR P050102504A AR P050102504 A ARP050102504 A AR P050102504A AR 049446 A1 AR049446 A1 AR 049446A1
Authority
AR
Argentina
Prior art keywords
formula
cycloalkyl
compound
salt
alkyl
Prior art date
Application number
ARP050102504A
Other languages
English (en)
Original Assignee
Warner Lambert Co
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=35295367&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=AR049446(A1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Warner Lambert Co filed Critical Warner Lambert Co
Publication of AR049446A1 publication Critical patent/AR049446A1/es

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C253/00Preparation of carboxylic acid nitriles
    • C07C253/30Preparation of carboxylic acid nitriles by reactions not involving the formation of cyano groups
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12PFERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
    • C12P13/00Preparation of nitrogen-containing organic compounds
    • C12P13/02Amides, e.g. chloramphenicol or polyamides; Imides or polyimides; Urethanes, i.e. compounds comprising N-C=O structural element or polyurethanes
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C227/00Preparation of compounds containing amino and carboxyl groups bound to the same carbon skeleton
    • C07C227/12Formation of amino and carboxyl groups
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/08Antiepileptics; Anticonvulsants
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C227/00Preparation of compounds containing amino and carboxyl groups bound to the same carbon skeleton
    • C07C227/04Formation of amino groups in compounds containing carboxyl groups
    • C07C227/06Formation of amino groups in compounds containing carboxyl groups by addition or substitution reactions, without increasing the number of carbon atoms in the carbon skeleton of the acid
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C227/00Preparation of compounds containing amino and carboxyl groups bound to the same carbon skeleton
    • C07C227/14Preparation of compounds containing amino and carboxyl groups bound to the same carbon skeleton from compounds containing already amino and carboxyl groups or derivatives thereof
    • C07C227/18Preparation of compounds containing amino and carboxyl groups bound to the same carbon skeleton from compounds containing already amino and carboxyl groups or derivatives thereof by reactions involving amino or carboxyl groups, e.g. hydrolysis of esters or amides, by formation of halides, salts or esters
    • C07C227/20Preparation of compounds containing amino and carboxyl groups bound to the same carbon skeleton from compounds containing already amino and carboxyl groups or derivatives thereof by reactions involving amino or carboxyl groups, e.g. hydrolysis of esters or amides, by formation of halides, salts or esters by hydrolysis of N-acylated amino-acids or derivatives thereof, e.g. hydrolysis of carbamates
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C227/00Preparation of compounds containing amino and carboxyl groups bound to the same carbon skeleton
    • C07C227/22Preparation of compounds containing amino and carboxyl groups bound to the same carbon skeleton from lactams, cyclic ketones or cyclic oximes, e.g. by reactions involving Beckmann rearrangement
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C229/00Compounds containing amino and carboxyl groups bound to the same carbon skeleton
    • C07C229/02Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino and carboxyl groups bound to acyclic carbon atoms of the same carbon skeleton
    • C07C229/04Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino and carboxyl groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being acyclic and saturated
    • C07C229/24Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino and carboxyl groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being acyclic and saturated having more than one carboxyl group bound to the carbon skeleton, e.g. aspartic acid
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C255/00Carboxylic acid nitriles
    • C07C255/01Carboxylic acid nitriles having cyano groups bound to acyclic carbon atoms
    • C07C255/19Carboxylic acid nitriles having cyano groups bound to acyclic carbon atoms containing cyano groups and carboxyl groups, other than cyano groups, bound to the same saturated acyclic carbon skeleton
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D207/00Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D207/02Heterocyclic 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
    • C07D207/18Heterocyclic 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 one double bond between ring members or between a ring member and a non-ring member
    • C07D207/22Heterocyclic 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 one double bond between ring members or between a ring member and a non-ring member 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
    • C07D207/24Oxygen or sulfur atoms
    • C07D207/262-Pyrrolidones
    • C07D207/2732-Pyrrolidones 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 other ring carbon atoms
    • C07D207/277Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12PFERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
    • C12P13/00Preparation of nitrogen-containing organic compounds
    • C12P13/001Amines; Imines
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12PFERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
    • C12P13/00Preparation of nitrogen-containing organic compounds
    • C12P13/002Nitriles (-CN)
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12PFERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
    • C12P7/00Preparation of oxygen-containing organic compounds
    • C12P7/40Preparation of oxygen-containing organic compounds containing a carboxyl group including Peroxycarboxylic acids
    • C12P7/42Hydroxy-carboxylic acids

Abstract

Reinvidicacion 1: Un método para preparar un compuesto de formula (1), o un complejo, sal, solvato o hidrato de éste aceptable desde un punto de vista farmacéutico, en el que R1 y R2 son diferentes y cada uno se selecciona de manera independiente de átomo de hidrogeno, alquilo C1-12, cicloalquilo C3-12, y cicloalquilo C3-12 sustituido, método que comprende: (a) hacer reaccionar un comuesto de formula (2), o una sal de éste, con un ácido y agua para rendir el compuesto de formula (1) o una sal de éste; y (b) opcionalmente convertir el compuesto de formula (1) o una sal de éste en un complejo, sal, solvato o hidrato aceptable desde un punto de vista farmacéutico, en el que R1 y R2 en la formula (2) son como se han definido en la formula (1) Reivindicacion 8: Un compuesto de formula (3), incluyendo sales de éste, en el que R1 y R2 son diferentes y cada uno se selecciona de manera independiente de átomo de hidrogeno, alquilo C1-12, cicloalquilo C3-12, y cicloalquilo C3-12 sustituido, siempre que cuando uno de los sustituyentes representados por R1 o R2 es un átomo de hidrogeno, el otro sustituyente no es metilo; y R5 y R6 se seleccionan de manera independiente de átomo de hidrogeno, alquilo C1-12, cicloalquilo C3-12, o aril-alquilo C1-6, siempre que R5 y R6 sean diferentes si no son los dos átomos de hidrogeno.
ARP050102504A 2004-06-21 2005-06-17 Preparacion de pregabalina ((s)-(+)-aminometil-5-metilhexanoico) y compuestos relacionados AR049446A1 (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US58167104P 2004-06-21 2004-06-21
US62903404P 2004-11-18 2004-11-18

Publications (1)

Publication Number Publication Date
AR049446A1 true AR049446A1 (es) 2006-08-02

Family

ID=35295367

Family Applications (1)

Application Number Title Priority Date Filing Date
ARP050102504A AR049446A1 (es) 2004-06-21 2005-06-17 Preparacion de pregabalina ((s)-(+)-aminometil-5-metilhexanoico) y compuestos relacionados

Country Status (33)

Country Link
US (4) US20050283023A1 (es)
EP (1) EP1831154B1 (es)
JP (5) JP4174551B2 (es)
KR (3) KR100847928B1 (es)
CN (2) CN1972904B (es)
AP (1) AP2466A (es)
AR (1) AR049446A1 (es)
AT (1) ATE455093T1 (es)
AU (1) AU2005256945B2 (es)
BR (1) BRPI0512347B8 (es)
CA (1) CA2571040C (es)
CR (2) CR8765A (es)
CY (1) CY1110337T1 (es)
DE (1) DE602005018965D1 (es)
DK (1) DK1831154T3 (es)
EA (3) EA015418B1 (es)
ES (1) ES2336014T3 (es)
GE (1) GEP20104895B (es)
HK (2) HK1104024A1 (es)
HR (1) HRP20100054T1 (es)
IL (1) IL179614A0 (es)
MA (1) MA28674B1 (es)
ME (1) ME01067B (es)
MX (1) MXPA06014228A (es)
NO (1) NO338097B1 (es)
NZ (1) NZ552220A (es)
PL (1) PL1831154T3 (es)
PT (1) PT1831154E (es)
RS (1) RS51210B (es)
SI (1) SI1831154T1 (es)
TW (6) TWI377191B (es)
UA (1) UA83575C2 (es)
WO (1) WO2006000904A2 (es)

Families Citing this family (45)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6001876A (en) 1996-07-24 1999-12-14 Warner-Lambert Company Isobutylgaba and its derivatives for the treatment of pain
US7417165B2 (en) 2005-04-06 2008-08-26 Teva Pharmaceutical Industries Ltd. Crystalline forms of pregabalin
US7488846B2 (en) 2005-04-11 2009-02-10 Teva Pharmaceuical Industries Ltd. Pregabalin free of lactam and a process for preparation thereof
MX2007012606A (es) * 2005-04-11 2008-01-11 Teva Pharma Proceso para elaborar (s)-pregabalina.
JP2008505980A (ja) 2005-05-10 2008-02-28 テバ ファーマシューティカル インダストリーズ リミティド イソブチルグルタル酸を有さないプレガバリン及びその調製方法
EP1879851B1 (en) 2005-05-10 2010-11-03 Teva Pharmaceutical Industries Ltd Method for the preparation of pregabalin and salts thereof
ATE523484T1 (de) * 2005-05-10 2011-09-15 Teva Pharma Optische lösung a us 3-carbamoylmethyl-5-methyl- hexansäure
CZ297970B6 (cs) * 2005-08-10 2007-05-09 Zentiva, A. S Zpusob výroby (S)-3-(aminomethyl)-5-methyl-hexanové kyseliny (pregabalinu)
ES2398579T3 (es) 2005-09-19 2013-03-20 Teva Pharmaceutical Industries Ltd Una síntesis asimétrica de ácido (S)-(+)-3-(aminometil)-5-metilhexanoico
EP2019817A2 (en) 2006-05-24 2009-02-04 Teva Pharmaceutical Industries Ltd. Processes for the preparation of r-(+)-3-(carbamoyl methyl)-5-methylhexanoic acid and salts thereof
WO2007143113A2 (en) * 2006-05-31 2007-12-13 Teva Pharmaceutical Industries Ltd. The use of enzymatic resolution for the preparation of intermediates of pregabalin
WO2007143152A2 (en) * 2006-05-31 2007-12-13 Teva Pharmaceutical Industries Ltd. Preparation of (s)-pregabalin-nitrile
US8097754B2 (en) 2007-03-22 2012-01-17 Teva Pharmaceutical Industries Ltd. Synthesis of (S)-(+)-3-(aminomethyl)-5-methyl hexanoic acid
EP1992609A1 (en) * 2007-05-14 2008-11-19 Dipharma Francis S.r.l. A process for the preparation of a (S)(+)-3-(aminomethyl)-5-methylhexanoic acid
JP5157576B2 (ja) 2007-05-14 2013-03-06 住友化学株式会社 光学活性2−アルキル−1,1,3−トリアルコキシカルボニルプロパンの製造方法
KR100846419B1 (ko) * 2007-08-10 2008-07-15 한국과학기술원 프레가발린의 신규한 제조 방법
US20090062393A1 (en) * 2007-08-29 2009-03-05 Protia, Llc Deuterium-enriched pregabalin
WO2009046309A2 (en) * 2007-10-03 2009-04-09 Teva Pharmaceutical Industries Ltd. Pregabalin -4-eliminate, pregabalin 5-eliminate, their use as reference marker and standard, and method to produce pregabalin containing low levels thereof
ITMI20072262A1 (it) 2007-12-03 2009-06-04 Dipharma Francis Srl Procedimento per la preparazione di acido (s)(+)-3-(amminometil)-5-metilesanoico
US20100312010A1 (en) * 2007-12-18 2010-12-09 Watson Pharma Private Limited Process for the Preparation of (S)-Pregabalin
AU2008339583A1 (en) * 2007-12-26 2009-07-02 Generics [Uk] Limited Processes to pregabalin
SG176464A1 (en) * 2008-05-09 2011-12-29 Agency Science Tech & Res Diagnosis and treatment of kawasaki disease
MX2010012698A (es) 2008-05-21 2011-03-15 Sandoz Ag Proceso para la hidrolisis enzimatica estereoselectiva del ester del acido 5-metil-3-nitro-metil-hexanoico.
US20090312560A1 (en) * 2008-06-10 2009-12-17 Lambertus Thijs Processes for making pregabalin and intermediates therefor
KR20100107500A (ko) * 2008-06-23 2010-10-05 테바 파마슈티컬 인더스트리즈 리미티드 (s) 또는 (r)-이소-부틸-글루타릭 에스테르의 입체선택적 효소 합성방법
WO2010070593A2 (en) 2008-12-19 2010-06-24 Pfizer Ireland Pharmaceuticals Malonate esters
IT1394292B1 (it) 2009-05-07 2012-06-06 Dipharma Francis Srl Procedimento per la sintesi di pregabalina
WO2011141923A2 (en) 2010-05-14 2011-11-17 Lupin Limited Improved synthesis of optically pure (s) - 3-cyano-5-methyl-hexanoic acid alkyl ester, an intermediate of (s)- pregabalin
WO2012025861A1 (en) 2010-08-23 2012-03-01 Pfizer Manufacturing Ireland Process for the preparation of ( s ) - 3 - cyano - 5 - methylhexanoic acid derivatives adn of pregabalin
WO2012059797A1 (en) * 2010-11-04 2012-05-10 Lupin Limited Process for synthesis of (s) - pregabalin
KR101306585B1 (ko) * 2011-04-14 2013-09-10 한국외국어대학교 연구산학협력단 프레가발린의 제조방법
CN102952057B (zh) * 2012-11-07 2015-09-09 浙江普洛家园药业有限公司 一种4-异丁基吡咯烷-2-酮的制备方法
JP6225490B2 (ja) * 2013-05-31 2017-11-08 大日本印刷株式会社 医薬品包装体
US10076550B2 (en) * 2014-06-25 2018-09-18 Council Of Scientific & Industrial Research Synergistic pharmaceutical composition for gastroinestinal disorders
WO2016075082A1 (en) 2014-11-10 2016-05-19 Sandoz Ag Stereoselective reductive amination of alpha-chiral aldehydes using omega-transaminases for the synthesis of precursors of pregabalin and brivaracetam
CN104557576B (zh) * 2014-12-19 2019-07-19 浙江华海药业股份有限公司 一种高纯度普瑞巴林的制备方法
CN105348125A (zh) * 2015-11-26 2016-02-24 太仓运通生物化工有限公司 一种以异戊醛为原料合成普瑞巴林的方法
CN107445864B (zh) * 2017-08-09 2020-01-17 无锡殷达尼龙有限公司 一种纯化长碳链氰基酸产物的方法
CN108358799B (zh) * 2018-04-24 2020-11-10 贵州师范大学 一种普瑞巴林的制备方法
CN109503403B (zh) * 2018-12-21 2021-11-16 卓和药业集团股份有限公司 一种普瑞巴林的拆分方法
CN113248416B (zh) * 2020-02-10 2024-03-26 江西博腾药业有限公司 1-((苄氧基)羰基)-4-乙基吡咯烷-3-羧酸的制备方法及其应用
EP4103168A4 (en) 2020-02-14 2024-04-24 Council Scient Ind Res PROCESS FOR THE PRODUCTION OF GAMMA-AMINOBUTRY ACIDS AND THEIR ANALOGUES
CN111205288B (zh) 2020-02-19 2021-03-30 四川大学 一种(1S,12bS)内酰胺酯化合物的合成方法
CN113651717A (zh) * 2021-08-05 2021-11-16 浙江工业大学 一种光学纯异丁基丁二腈的消旋方法
CN113880724A (zh) * 2021-12-06 2022-01-04 南京桦冠生物技术有限公司 一种3-(2-氨基苯基)-2-丙烯酸酯的制备方法

Family Cites Families (28)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3125583A (en) * 1964-03-17 Hjnc oxchaxohxchc o oh
US637767A (en) * 1899-09-25 1899-11-28 Gaylard W Denyes Grain-drill.
SU452196A1 (ru) * 1973-02-12 2001-09-20 Филиал Всесоюзного Научно-Исследовательского Химико-Фармацевтического Института Им. Серго Орджоникидзе СПОСОБ ПОЛУЧЕНИЯ γ-АМИНОМАСЛЯНОЙ КИСЛОТЫ
JPS60338B2 (ja) * 1980-12-16 1985-01-07 日本新薬株式会社 酪酸誘導体の製法
US4428887A (en) * 1982-07-14 1984-01-31 Monsanto Company Method of producing mono-substituted terminal diesters
US5618710A (en) * 1990-08-03 1997-04-08 Vertex Pharmaceuticals, Inc. Crosslinked enzyme crystals
US6197819B1 (en) * 1990-11-27 2001-03-06 Northwestern University Gamma amino butyric acid analogs and optical isomers
US5616793A (en) * 1995-06-02 1997-04-01 Warner-Lambert Company Methods of making (S)-3-(aminomethyl)-5-methylhexanoic acid
US5637767A (en) * 1995-06-07 1997-06-10 Warner-Lambert Company Method of making (S)-3-(aminomethyl)-5-methylhexanoic acid
DE19623142A1 (de) * 1996-06-10 1997-12-11 Huels Chemische Werke Ag Enantiomerenangereicherte, durch einen tertiären Kohlenwasserstoffrest substituierte Malonsäuremonoester sowie deren Herstellung
US6001876A (en) * 1996-07-24 1999-12-14 Warner-Lambert Company Isobutylgaba and its derivatives for the treatment of pain
JPH10245369A (ja) * 1997-03-03 1998-09-14 Ajinomoto Co Inc セリン誘導体の製造方法
US6329429B1 (en) * 1997-06-25 2001-12-11 Warner-Lambert Company Use of GABA analogs such as Gabapentin in the manufacture of a medicament for treating inflammatory diseases
AU9019198A (en) * 1997-08-19 1999-03-08 Warner-Lambert Company Methods for treating physiological conditions associated with the use, or sequelae of use, of cocaine or other psychomotor stimulants
AU8668598A (en) * 1997-08-20 1999-03-08 University Of Oklahoma, The Gaba analogs to prevent and treat gastrointestinal damage
US6127418A (en) * 1997-08-20 2000-10-03 Warner-Lambert Company GABA analogs to prevent and treat gastrointestinal damage
RU2143002C1 (ru) * 1997-12-24 1999-12-20 Акционерное общество открытого типа "Мосагроген" СПОСОБ ПОЛУЧЕНИЯ γ-АМИНОМАСЛЯНОЙ КИСЛОТЫ
WO2000002546A2 (en) * 1998-07-09 2000-01-20 Warner-Lambert Company Use of caba-analogues for treating insomnia
JP2002520286A (ja) * 1998-07-09 2002-07-09 ワーナー−ランバート・カンパニー Gaba類縁体及びカフェインを含んでなる組成物
EP1121114B1 (en) * 1998-10-16 2007-01-10 Warner-Lambert Company Llc Use of gaba analogs for the manufacture of a medicament for the treatment of mania and bipolar disorders
EA004934B1 (ru) * 2000-01-27 2004-10-28 Уорнер-Ламберт Компани Асимметрический синтез прегабалина
GB0004297D0 (en) * 2000-02-23 2000-04-12 Ucb Sa 2-oxo-1 pyrrolidine derivatives process for preparing them and their uses
US6931007B2 (en) * 2001-07-25 2005-08-16 Longboard, Inc. System and method of serving data messages
EP1333087A1 (en) * 2002-02-05 2003-08-06 Avantium International B.V. Crosslinked enzyme aggregates and crosslinking agent therefore
US20030225149A1 (en) * 2002-04-30 2003-12-04 Blazecka Peter G. Process for preparing highly functionalized gamma-butyrolactams and gamma-amino acids
FR2849024B1 (fr) * 2002-12-20 2007-11-02 Aventis Pharma Sa Nouveaux composes chiraux derives d'esters de l'acide hexanoique, procede et intermediaires de preparation, utilisation a la synthese de l'acide 2-(bromomethyl)2-ethyl hexanoique chiral
JP2006061112A (ja) * 2004-08-30 2006-03-09 Sumitomo Chemical Co Ltd 光学活性な2−(シクロペンチルメチル)−マロン酸モノエステルの製造方法
WO2007143113A2 (en) * 2006-05-31 2007-12-13 Teva Pharmaceutical Industries Ltd. The use of enzymatic resolution for the preparation of intermediates of pregabalin

Also Published As

Publication number Publication date
TWI399361B (zh) 2013-06-21
JP4800346B2 (ja) 2011-10-26
KR20080015524A (ko) 2008-02-19
TW200846307A (en) 2008-12-01
MA28674B1 (fr) 2007-06-01
TWI396743B (zh) 2013-05-21
CR20110483A (es) 2011-10-24
TW200604139A (en) 2006-02-01
AP2006003846A0 (en) 2006-12-31
JP2008088191A (ja) 2008-04-17
GEP20104895B (en) 2010-02-25
TW200902481A (en) 2009-01-16
EA200800908A1 (ru) 2008-12-30
TWI405747B (zh) 2013-08-21
JP4174551B2 (ja) 2008-11-05
ATE455093T1 (de) 2010-01-15
BRPI0512347B8 (pt) 2021-05-25
CN1972904A (zh) 2007-05-30
US8134023B2 (en) 2012-03-13
US7838686B2 (en) 2010-11-23
CA2571040C (en) 2009-09-15
HK1104024A1 (en) 2008-01-04
EA011765B1 (ru) 2009-06-30
JP4966183B2 (ja) 2012-07-04
US20050283023A1 (en) 2005-12-22
BRPI0512347A (pt) 2008-03-04
US20120015412A1 (en) 2012-01-19
CN1972904B (zh) 2011-02-02
NZ552220A (en) 2010-08-27
NO338097B1 (no) 2016-08-01
UA83575C2 (uk) 2008-07-25
MXPA06014228A (es) 2007-02-14
KR20080015152A (ko) 2008-02-18
KR100847928B1 (ko) 2008-07-22
SI1831154T1 (sl) 2010-03-31
US20110065168A1 (en) 2011-03-17
DE602005018965D1 (de) 2010-03-04
TWI357405B (en) 2012-02-01
US8044227B2 (en) 2011-10-25
ME01067B (me) 2012-10-20
HK1161307A1 (en) 2012-08-24
KR100847927B1 (ko) 2008-07-22
TWI377191B (en) 2012-11-21
AP2466A (en) 2012-09-17
EA015418B1 (ru) 2011-08-30
RS51210B (sr) 2010-12-31
WO2006000904A3 (en) 2006-04-27
AU2005256945A1 (en) 2006-01-05
EP1831154A2 (en) 2007-09-12
CN102102114B (zh) 2013-08-14
TW200900375A (en) 2009-01-01
WO2006000904A2 (en) 2006-01-05
AU2005256945B2 (en) 2008-11-13
ES2336014T3 (es) 2010-04-07
CR8765A (es) 2008-01-02
NO20065329L (no) 2006-12-19
DK1831154T3 (da) 2010-04-12
KR100847929B1 (ko) 2008-07-22
KR20080015153A (ko) 2008-02-18
CN102102114A (zh) 2011-06-22
PT1831154E (pt) 2010-02-19
EA200800909A1 (ru) 2008-08-29
TW200846474A (en) 2008-12-01
JP2008504252A (ja) 2008-02-14
CY1110337T1 (el) 2015-01-14
BRPI0512347B1 (pt) 2018-03-20
TW200846306A (en) 2008-12-01
JP4782101B2 (ja) 2011-09-28
JP2008133289A (ja) 2008-06-12
JP2008110985A (ja) 2008-05-15
EP1831154B1 (en) 2010-01-13
PL1831154T3 (pl) 2010-05-31
JP4777332B2 (ja) 2011-09-21
JP2009022272A (ja) 2009-02-05
US20090042262A1 (en) 2009-02-12
HRP20100054T1 (hr) 2010-05-31
EA200602099A1 (ru) 2007-04-27
CA2571040A1 (en) 2006-01-05
TWI402248B (zh) 2013-07-21
IL179614A0 (en) 2007-05-15

Similar Documents

Publication Publication Date Title
AR049446A1 (es) Preparacion de pregabalina ((s)-(+)-aminometil-5-metilhexanoico) y compuestos relacionados
AR044874A1 (es) Derivados de 4- cianopirazol-3 - carboxamida, su preparacion y su aplicacion en terapeutica
AR046297A1 (es) Inhibidores de la dpp - iv metodos para prepararlos y composiciones farmaceuticas que los contienen como agente activo
PH12014502866A1 (en) Fungicidal heterocyclic carboxamides
CO6331462A2 (es) Compuesto de fenil pirrol o una sal farmaceuticamente aceptable del mismo con actividad activadora de la glucoquinasa
AR038536A1 (es) N-aril-2-oxazolidinona-5- carboxamidas y sus derivados
RU2018121834A (ru) Новое соединение бифенила или его соль
CR10034A (es) Derivados de oxadiazol
AR054560A1 (es) Espiropiperidina como inhibidores de beta-secretasa para el tratamiento de la enfermedad de alzheimer
AR047085A1 (es) Derivados de (3-oxo-3,4-dihidro-quinoxalina-2-il-amino)benzamida y compuestos relacionados como inhibidores de glucogeno fosforilasa para el tratamiento de diabetes y obesidad
BRPI0608732A2 (pt) composto ou um sal, hidrato, solvato, complexo ou pró-droga farmaceuticamente aceitável do mesmo, sal de um composto, processo para a preparação de um composto, uso de um composto, composição farmacêutica, e, produto
AR043436A1 (es) Tetrahidroisoquinolinas sustituidas para uso como moduladores 5-ht6
EP1724262A4 (en) 1- (2H) -ISOCHINOLONDERIVAT
PE20121047A1 (es) Derivados de tiazolilpiperidina como fungicidas
AR068950A1 (es) Derivados heterociclo biciclicos y metodos de uso de los mismos
AR046085A1 (es) Agonistas etilamino amino sustituidos del receptor beta 2 adrenergico
AR060604A1 (es) Nuevos arilamino n- heteroarilos como inhibidores de mek
AR067412A1 (es) Moduladores de propiedades farmaceuticas de productos terapeuticos
TW200621694A (en) Substituted n-sulfonylaminobenzyl-2-phenoxyacetamide compounds
MX360667B (es) Derivados de etinilo como moduladores alostericos del receptor de glutamato metabotropico del subtipo 5 (mglur5).
EA201071012A1 (ru) Производные азетидинов, способ их получения и применение их в терапии
AR060962A1 (es) Proceso de preparacion de derivados de quinazolina e intermediarios de sintesis
BR112013015604A2 (pt) novo derivado de isoquinolina substituído
AR040570A1 (es) Deriados de acilaminotiazol, su preparacion y su aplicacion en terapeutica
AR045007A1 (es) Compuestos de quinazolinona sustituidos con arilamina

Legal Events

Date Code Title Description
FG Grant, registration