BR9809113A - Novos intermediários e processo para sua preparação - Google Patents

Novos intermediários e processo para sua preparação

Info

Publication number
BR9809113A
BR9809113A BR9809113-1A BR9809113A BR9809113A BR 9809113 A BR9809113 A BR 9809113A BR 9809113 A BR9809113 A BR 9809113A BR 9809113 A BR9809113 A BR 9809113A
Authority
BR
Brazil
Prior art keywords
preparation
new intermediaries
thienyl
intermediaries
new
Prior art date
Application number
BR9809113-1A
Other languages
English (en)
Other versions
BR9809113B1 (pt
Inventor
Alain Heymes
Bertrand Castro
Maria Bakonyi
Marianna Csatarine Nagy
Leventene Molnar
Original Assignee
Sanofi Synthelabo Inc
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 Synthelabo Inc filed Critical Sanofi Synthelabo Inc
Publication of BR9809113A publication Critical patent/BR9809113A/pt
Publication of BR9809113B1 publication Critical patent/BR9809113B1/pt

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D495/00Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
    • C07D495/02Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
    • C07D495/04Ortho-condensed systems
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D333/00Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom
    • C07D333/02Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings
    • C07D333/04Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom
    • C07D333/06Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to the ring carbon atoms
    • C07D333/14Radicals substituted by singly bound hetero atoms other than halogen
    • C07D333/20Radicals substituted by singly bound hetero atoms other than halogen by nitrogen atoms

Abstract

"NOVOS INTERMEDIáRIOS E PROCESSO PARA SUA PREPARAçãO" Trata-se de um processo para a preparação de [2 - (2 - tienil) -etil - amino] - (2 -halogeno-fenil) -acetonitrilas da fórmula genérica (I), a partir de 2 - (2 - tienil) -etil-amina, cianeto de metal alcalino e o-halogeno-benzaldeído. Os compostos da fórmula genérica (I) são internediários valiosos.
BRPI9809113-1A 1997-05-13 1998-05-11 [2-(2-tienil) -etilamino] -(2-halogeno-fenil) -acetonitilas como intermediários e processo para sua preparação. BR9809113B1 (pt)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
HU9700886A HU225504B1 (en) 1997-05-13 1997-05-13 Novel halophenyl-(2-(2-thienyl)-ethylamino)-acetonitriles and process for producing them
HUP9700886 1997-05-13
PCT/HU1998/000046 WO1998051682A1 (en) 1997-05-13 1998-05-11 New intermediates and process for the preparation thereof

Publications (2)

Publication Number Publication Date
BR9809113A true BR9809113A (pt) 2000-08-01
BR9809113B1 BR9809113B1 (pt) 2010-03-09

Family

ID=89995121

Family Applications (1)

Application Number Title Priority Date Filing Date
BRPI9809113-1A BR9809113B1 (pt) 1997-05-13 1998-05-11 [2-(2-tienil) -etilamino] -(2-halogeno-fenil) -acetonitilas como intermediários e processo para sua preparação.

Country Status (14)

Country Link
US (1) US6215005B1 (pt)
EP (1) EP0981525B1 (pt)
JP (1) JP4279903B2 (pt)
AT (1) ATE258551T1 (pt)
AU (1) AU7444698A (pt)
BR (1) BR9809113B1 (pt)
CA (1) CA2288637C (pt)
DE (1) DE69821347T2 (pt)
DK (1) DK0981525T3 (pt)
ES (1) ES2213900T3 (pt)
HU (1) HU225504B1 (pt)
NO (1) NO325305B1 (pt)
PT (1) PT981525E (pt)
WO (1) WO1998051682A1 (pt)

Families Citing this family (18)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
HU226421B1 (en) * 1998-11-09 2008-12-29 Sanofi Aventis Process for racemizing optically active 2-(2-chlorophenyl)-2-(2-(2-thienyl)-ethylamino)-acetamides
US6495691B1 (en) 2001-07-06 2002-12-17 Brantford Chemicals Inc. Process for the preparation of tetrahydrothieno[3,2-c]pyridine derivatives
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
HUP0200438A3 (en) * 2002-02-06 2003-10-28 Egis Gyogyszergyar Nyilvanosan Novel clopidogrel hydrochloride polymorphs, process for the preparation thereof, their use and pharmaceutical compositions containing them
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
EP1603920A1 (en) 2003-03-12 2005-12-14 Cadila Healthcare Ltd. Polymorph and amorphous form of (s)-(+)-clopidogrel bisulfate
US20040250673A1 (en) * 2003-06-10 2004-12-16 Salerno Paul Michael Ergonomic pedal board
GB0321256D0 (en) 2003-09-11 2003-10-08 Generics Uk Ltd Novel crystalline compounds
EP1680430B1 (en) 2003-11-03 2010-01-20 Cadila Healthcare Ltd. Processes for preparing form i of (s)-(+)- clopidogrel bisulfate
US20060154957A1 (en) * 2004-09-21 2006-07-13 Nina Finkelstein Crystalline clopidogrel hydrobromide and processes for preparation thereof
TW200640932A (en) * 2005-02-24 2006-12-01 Teva Pharma Clopidogrel base suitable for pharmaceutical formulation and preparation thereof
EP1902058A2 (en) 2005-07-12 2008-03-26 RPG Life Sciences Limited A process for preparation of methyl-(+)-(s)-alpha-(2-chlorophenyl)-6,7-dihydrothieno(3,2-c)pyridine-5(4h)-acetic acid methyl ester or salts thereof having higher chiral purity and products thereof
KR20090013794A (ko) * 2006-04-27 2009-02-05 인드-스위프트 래버러토리즈 리미티드 클로피도그렐 히드로겐 설페이트의 다형태의 제조방법
US20090247569A1 (en) * 2006-08-03 2009-10-01 Claude Singer Process for Preparing Clopidogrel Bisulphate
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
EP2346879A1 (en) * 2008-10-24 2011-07-27 Sandoz AG A process for the preparation of s-clopidogrel

Family Cites Families (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2508455A1 (fr) 1981-06-30 1982-12-31 Sanofi Sa Procede de preparation de derives des (thienyl-2)- et (thienyl-3)-2 ethylamines
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
FR2608607B1 (fr) 1986-12-23 1989-04-28 Sanofi Sa Procede de preparation de thienylethylamines et dithienylethylamines ainsi obtenues
FR2623810B2 (fr) 1987-02-17 1992-01-24 Sanofi Sa Sels de l'alpha-(tetrahydro-4,5,6,7 thieno(3,2-c) pyridyl-5) (chloro-2 phenyl) -acetate de methyle dextrogyre et compositions pharmaceutiques en contenant
FR2614619B1 (fr) 1987-04-29 1989-09-15 Sanofi Sa Procede de preparation de n-((chloro-2)-benzyl) (thienyl-2)-2 ethylamine
FR2652575B1 (fr) * 1989-09-29 1992-01-24 Sanofi Sa Procede de preparation d'acides alpha-bromo phenylacetiques.
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.
CA2265886A1 (en) * 1996-09-12 1998-03-19 Rhone-Poulenc Rorer Pharmaceuticals Inc. Stereospecific preparation of chiral 1-aryl- and 1-heteroaryl-2-substituted ethyl-2-amines

Also Published As

Publication number Publication date
HUP9700886A2 (hu) 1999-09-28
NO995531D0 (no) 1999-11-12
AU7444698A (en) 1998-12-08
US6215005B1 (en) 2001-04-10
NO995531L (no) 1999-12-13
NO325305B1 (no) 2008-03-25
DE69821347D1 (de) 2004-03-04
EP0981525B1 (en) 2004-01-28
PT981525E (pt) 2004-05-31
ES2213900T3 (es) 2004-09-01
HU225504B1 (en) 2007-01-29
DE69821347T2 (de) 2004-12-02
WO1998051682A1 (en) 1998-11-19
JP2001525817A (ja) 2001-12-11
BR9809113B1 (pt) 2010-03-09
EP0981525A1 (en) 2000-03-01
CA2288637C (en) 2005-11-15
DK0981525T3 (da) 2004-05-10
CA2288637A1 (en) 1998-11-19
ATE258551T1 (de) 2004-02-15
JP4279903B2 (ja) 2009-06-17
HU9700886D0 (en) 1997-07-28
HUP9700886A3 (en) 2000-06-28

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Legal Events

Date Code Title Description
B25G Requested change of headquarter approved
B06A Patent application procedure suspended [chapter 6.1 patent gazette]
B25D Requested change of name of applicant approved

Owner name: SANOFI-AVENTIS (FR)

Free format text: ALTERADO DE: SANOFI-SYNTHELABO

B09A Decision: intention to grant [chapter 9.1 patent gazette]
B16A Patent or certificate of addition of invention granted [chapter 16.1 patent gazette]

Free format text: PRAZO DE VALIDADE: 10 (DEZ) ANOS CONTADOS A PARTIR DE 09/03/2010, OBSERVADAS AS CONDICOES LEGAIS.

B21A Patent or certificate of addition expired [chapter 21.1 patent gazette]

Free format text: PATENTE EXTINTA EM 09.03.2020