ES2078956T3 - Procedimiento de preparacion de derivados fenilaceticos de tienopiridinas y de acidos alfa-bromofenilaceticos intermedios. - Google Patents

Procedimiento de preparacion de derivados fenilaceticos de tienopiridinas y de acidos alfa-bromofenilaceticos intermedios.

Info

Publication number
ES2078956T3
ES2078956T3 ES90401828T ES90401828T ES2078956T3 ES 2078956 T3 ES2078956 T3 ES 2078956T3 ES 90401828 T ES90401828 T ES 90401828T ES 90401828 T ES90401828 T ES 90401828T ES 2078956 T3 ES2078956 T3 ES 2078956T3
Authority
ES
Spain
Prior art keywords
preparation
formula
thenopyridines
procedure
phenylacetic
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.)
Expired - Lifetime
Application number
ES90401828T
Other languages
English (en)
Inventor
Michel Bouisset
Joel Radisson
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Sanofi SA
Original Assignee
Sanofi SA
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
Application filed by Sanofi SA filed Critical Sanofi SA
Application granted granted Critical
Publication of ES2078956T3 publication Critical patent/ES2078956T3/es
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
    • C07C51/16—Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation
    • C07C51/21—Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation with molecular oxygen
    • C07C51/23—Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation with molecular oxygen of oxygen-containing groups to carboxyl groups
    • C07C51/235—Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation with molecular oxygen of oxygen-containing groups to carboxyl groups of —CHO groups or primary alcohol groups
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
  • Pyridine Compounds (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
  • Measuring Or Testing Involving Enzymes Or Micro-Organisms (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Investigating Or Analysing Biological Materials (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

Abstract

EL PROCESO DE PREPARACION DE COMPUESTOS DE FORMULA I, EN LA CUAL R1 Y R2 IDENTICOS O DIFERENTES, REPRESENTAN CADA UNO EL HIDROGENO O UN HALOGENO, ESTA CARACTERIZADO SEGUN EL INVENTO EN QUE SE HACE REACCIONAR UN ALDEHIDO DE FORMULA (IV), EN LA CUAL R1 Y R2 TIENEN LA MISMA SIGNIFICACION QUE EN LA FORMULA I, CON CHBR3 Y KOH EN UNA MEZCLA DE DISOLVENTE INERTE Y AGUA. LOS PRODUCTOS OBTENIDOS SON INTERMEDIOS DE SINTESIS ESPECIALMENTE PARA EL COMPUESTO DE FORMULA III, PREPARADO POR REACCION DE UN ETER DEL ACIDO (ALFA)-BROMO (CLORO-2) FENILACETICO SOBRE LA TETRAHIDRO-4,5,6,7 TIENO [3,2-C] PIRIDINA EN PRESENCIA DE AL MENOS UN EQUIVALENTE DE BASE EN UN DISOLVENTE POLAR.
ES90401828T 1989-09-29 1990-06-26 Procedimiento de preparacion de derivados fenilaceticos de tienopiridinas y de acidos alfa-bromofenilaceticos intermedios. Expired - Lifetime ES2078956T3 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
FR8912787A FR2652575B1 (fr) 1989-09-29 1989-09-29 Procede de preparation d'acides alpha-bromo phenylacetiques.

Publications (1)

Publication Number Publication Date
ES2078956T3 true ES2078956T3 (es) 1996-01-01

Family

ID=9385964

Family Applications (1)

Application Number Title Priority Date Filing Date
ES90401828T Expired - Lifetime ES2078956T3 (es) 1989-09-29 1990-06-26 Procedimiento de preparacion de derivados fenilaceticos de tienopiridinas y de acidos alfa-bromofenilaceticos intermedios.

Country Status (28)

Country Link
US (1) US5036156A (es)
EP (1) EP0420706B1 (es)
JP (1) JP3176612B2 (es)
KR (1) KR910006201A (es)
AT (1) ATE128961T1 (es)
AU (1) AU627590B2 (es)
CA (1) CA2019301C (es)
DD (1) DD295851A5 (es)
DE (1) DE69022943T2 (es)
DK (1) DK0420706T3 (es)
ES (1) ES2078956T3 (es)
FI (1) FI903210A7 (es)
FR (1) FR2652575B1 (es)
GR (1) GR3017939T3 (es)
HU (1) HU207325B (es)
IE (1) IE70432B1 (es)
IL (1) IL94801A0 (es)
LV (1) LV11683B (es)
MA (1) MA21878A1 (es)
NO (1) NO902714L (es)
NZ (1) NZ234160A (es)
OA (1) OA09453A (es)
PL (1) PL285788A1 (es)
PT (1) PT94486B (es)
RU (1) RU1836373C (es)
TN (1) TNSN90089A1 (es)
YU (1) YU124590A (es)
ZA (1) ZA904830B (es)

Families Citing this family (34)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5189170A (en) * 1989-09-29 1993-02-23 Sanofi Process for the preparation of phenylacetic derivatives of thieno-pyridines
ES2079041T3 (es) * 1990-01-25 1996-01-01 Sanofi Sa Preparacion de 2-(2'-tienil)alquilaminas y sus derivados y sintesis de 4,5,6,7-tieno(3,2-c)piridina derivados de estos.
FR2664596B1 (fr) * 1990-07-10 1994-06-10 Sanofi Sa Procede de preparation d'un derive n-phenylacetique de tetrahydrothieno [3,2-c] pyridine et son intermediaire de synthese.
JP3127332B2 (ja) * 1993-05-10 2001-01-22 本田技研工業株式会社 自動二輪車用制動装置
JP3231169B2 (ja) * 1993-12-30 2001-11-19 本田技研工業株式会社 自動２輪車用制動装置
HU225503B1 (en) * 1997-05-13 2007-01-29 Sanofi Aventis Novel 2-(2-halophenyl)-2-(2-(2-thienyl)-ethylamino)-acetamides and process for producing them
HU222283B1 (hu) * 1997-05-13 2003-05-28 Sanofi-Synthelabo Eljárás tieno[3,2-c]piridin-származékok előállítására
HU225504B1 (en) * 1997-05-13 2007-01-29 Sanofi Aventis Novel halophenyl-(2-(2-thienyl)-ethylamino)-acetonitriles and process for producing them
FR2769313B1 (fr) * 1997-10-06 2000-04-21 Sanofi Sa Derives d'esters hydroxyacetiques, leur procede de preparation et leur utilisation comme intermediaires de synthese
CA2436323C (en) * 2001-01-24 2012-02-21 Cadila Healthcare Ltd. Process for preparing clopidogrel
US6767913B2 (en) 2001-12-18 2004-07-27 Teva Pharmaceutical Industries Ltd. Crystal forms iii, iv, v, and novel amorphous form of clopidogrel hydrogensulfate, processes for their preparation, processes for the preparation of form i, compositions containing the new forms and methods of administering the new forms
US7074928B2 (en) 2002-01-11 2006-07-11 Teva Pharmaceutical Industries, Ltd. Polymorphs of clopidogrel hydrogensulfate
IL166593A0 (en) 2002-08-02 2006-01-15 Racemization and enantiomer separation of clopidogrel
US6800759B2 (en) * 2002-08-02 2004-10-05 Teva Pharmaceutical Industries Ltd. Racemization and enantiomer separation of clopidogrel
EP1606231A1 (en) * 2003-02-03 2005-12-21 Nadkarni, Sunil Sadanand Process for preparation of clopidogrel, its salts and pharmaceutical compositions
EP1603920A1 (en) 2003-03-12 2005-12-14 Cadila Healthcare Ltd. Polymorph and amorphous form of (s)-(+)-clopidogrel bisulfate
GB0321256D0 (en) 2003-09-11 2003-10-08 Generics Uk Ltd Novel crystalline compounds
DK1680430T3 (da) 2003-11-03 2010-05-25 Cadila Healthcare Ltd Fremgangsmåder til fremstilling af form I af (S)-(+)-Clopidogrel-bisulfat
JP2007513889A (ja) * 2004-09-21 2007-05-31 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 結晶性クロピドグレル臭酸塩及びその調製方法
US20060223845A1 (en) * 2005-02-24 2006-10-05 Eran Turgeman Clopidogrel base suitable for pharmaceutical formulation and preparation thereof
WO2006130852A1 (en) * 2005-06-02 2006-12-07 Dr. Reddy's Laboratories Ltd. Recovery of clopidogrel bisulfate
WO2007028337A1 (fr) * 2005-09-08 2007-03-15 Zhejiang Huahai Pharmaceutical Co., Ltd. Préparation de clopidogrel et ses composés analogues à base d'acétate de méthyl tétrahydrothiénopyridine
EP1980563A1 (en) 2007-04-09 2008-10-15 BATTULA, Srinivasa Reddy Procedure for the preparation of methyl (+)-(S)-Alpha-(O-chlorophenyl)-6,7-dihydrothieno-[3,2-C]pyridine-5(4H) acetate
BRPI0803101A2 (pt) * 2007-04-18 2014-04-22 Teva Pharma Processos melhores para preparação de clopidogrel
EP2107061A1 (en) 2008-04-02 2009-10-07 Krka Tovarna Zdravil, D.D., Novo Mesto Process for the preparation of optically enriched clopidogrel
US20090264460A1 (en) * 2008-04-21 2009-10-22 Mamta Mishra Clopidogrel pharmaceutical formulations
KR100990949B1 (ko) * 2008-06-09 2010-10-29 엔자이텍 주식회사 클로피도그렐 및 그의 유도체의 제조방법
US20110190502A1 (en) * 2008-10-24 2011-08-04 Sandoz Ag Process for the preparation of s-clopidogrel
US8563690B2 (en) * 2008-11-03 2013-10-22 The Board Of Trustees Of The University Of Illinois Modulation of platelet aggregation
CN101974016A (zh) * 2010-10-14 2011-02-16 天津药物研究院 酰胺类化合物及其制备方法和用途
CN102250114B (zh) * 2011-04-27 2014-02-26 青岛黄海制药有限责任公司 一种氯吡格雷及其硫酸盐的制备方法
CN102268012B (zh) * 2011-08-24 2014-04-09 天津药物研究院 噻唑衍生物、其制备方法和用途
CN103387497A (zh) * 2012-05-10 2013-11-13 深圳信立泰药业股份有限公司 一种氯吡格雷及其中间体α-溴代邻氯苯乙酸甲酯和噻吩乙胺基取代乙酸甲酯盐的制备方法
CN103450005B (zh) * 2012-06-01 2016-07-06 深圳信立泰药业股份有限公司 一种氯吡格雷及其中间体α-溴代邻氯苯乙酸和α-噻吩乙胺基取代乙酸盐酸盐的制备方法

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2778851A (en) * 1953-09-03 1957-01-22 Dow Chemical Co Preparation of alpha-chloro-alpha-methyl aliphatic acids and acid-chlorides
EP0011279B1 (en) * 1978-11-14 1982-05-05 Sagami Chemical Research Center Process for the preparation of aromatically substituted acetic acids
JPS5935370B2 (ja) * 1978-11-14 1984-08-28 財団法人相模中央化学研究所 芳香族酢酸の製造方法
US4289697A (en) 1980-10-15 1981-09-15 American Home Products Corporation 5-Substituted 4-hydroxy-2,3-alkylene thiazolium salts
FR2530247B1 (fr) * 1982-07-13 1986-05-16 Sanofi Sa Nouveaux derives de la thieno (3, 2-c) pyridine, leur procede de preparation et leur application therapeutique

Also Published As

Publication number Publication date
DD295851A5 (de) 1991-11-14
HUT55338A (en) 1991-05-28
DE69022943T2 (de) 1996-04-25
PT94486B (pt) 1997-02-28
YU124590A (en) 1991-10-31
AU627590B2 (en) 1992-08-27
PL285788A1 (en) 1991-08-12
LV11683A (lv) 1997-02-20
HU207325B (en) 1993-03-29
NZ234160A (en) 1992-08-26
RU1836373C (ru) 1993-08-23
NO902714D0 (no) 1990-06-19
JP3176612B2 (ja) 2001-06-18
US5036156A (en) 1991-07-30
EP0420706A2 (fr) 1991-04-03
FR2652575A1 (fr) 1991-04-05
FR2652575B1 (fr) 1992-01-24
CA2019301C (en) 2000-09-05
ATE128961T1 (de) 1995-10-15
EP0420706B1 (fr) 1995-10-11
DE69022943D1 (de) 1995-11-16
FI903210A0 (fi) 1990-06-26
NO902714L (no) 1991-04-02
KR910006201A (ko) 1991-04-27
AU5754690A (en) 1991-04-11
IE902179A1 (en) 1991-04-10
IL94801A0 (en) 1991-04-15
LV11683B (en) 1997-08-20
OA09453A (fr) 1992-10-15
EP0420706A3 (en) 1992-03-04
JPH03120286A (ja) 1991-05-22
GR3017939T3 (en) 1996-02-29
HU903995D0 (en) 1990-11-28
CA2019301A1 (en) 1991-03-29
TNSN90089A1 (fr) 1991-03-05
MA21878A1 (fr) 1990-12-31
FI903210A7 (fi) 1991-03-30
ZA904830B (en) 1992-02-26
IE70432B1 (en) 1996-11-27
PT94486A (pt) 1991-05-22
DK0420706T3 (da) 1996-02-05

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