JP2007512260A5 - - Google Patents

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Publication number
JP2007512260A5
JP2007512260A5 JP2006540130A JP2006540130A JP2007512260A5 JP 2007512260 A5 JP2007512260 A5 JP 2007512260A5 JP 2006540130 A JP2006540130 A JP 2006540130A JP 2006540130 A JP2006540130 A JP 2006540130A JP 2007512260 A5 JP2007512260 A5 JP 2007512260A5
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JP
Japan
Prior art keywords
treatment
type
heart
hypertension
pharmaceutical
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.)
Withdrawn
Application number
JP2006540130A
Other languages
English (en)
Japanese (ja)
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JP2007512260A (ja
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Publication date
Application filed filed Critical
Priority claimed from PCT/CH2004/000688 external-priority patent/WO2005051909A1/de
Publication of JP2007512260A publication Critical patent/JP2007512260A/ja
Publication of JP2007512260A5 publication Critical patent/JP2007512260A5/ja
Withdrawn legal-status Critical Current

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JP2006540130A 2003-11-28 2004-11-15 {N−[1−(S)−カルボアルコキシ−3−フェニルプロピル]−S−アラニル−2S,3aR,7aS−オクタヒドロインドール−2−カルボン酸}化合物類の製造方法 Withdrawn JP2007512260A (ja)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
CH20382003 2003-11-28
PCT/CH2004/000688 WO2005051909A1 (de) 2003-11-28 2004-11-15 Verfahren zur herstellung von {n-[1-(s)-carbalkoxy-3-phenylpropyl]-s-alanyl-2s, 3ar, 7as-octahydroindol-2-carbonsäure}verbindungen

Publications (2)

Publication Number Publication Date
JP2007512260A JP2007512260A (ja) 2007-05-17
JP2007512260A5 true JP2007512260A5 (enExample) 2007-12-06

Family

ID=34624414

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2006540130A Withdrawn JP2007512260A (ja) 2003-11-28 2004-11-15 {N−[1−(S)−カルボアルコキシ−3−フェニルプロピル]−S−アラニル−2S,3aR,7aS−オクタヒドロインドール−2−カルボン酸}化合物類の製造方法

Country Status (4)

Country Link
US (1) US20070135513A1 (enExample)
EP (1) EP1689711A1 (enExample)
JP (1) JP2007512260A (enExample)
WO (1) WO2005051909A1 (enExample)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2007003947A2 (en) * 2005-07-05 2007-01-11 Cipla Limited Process for the synthesis of the ace inhibitor trandolapril
US7943655B2 (en) 2006-04-05 2011-05-17 Universitat Zurich Polymorphic and pseudopolymorphic forms of trandolaprilat, pharmaceutical compositions and methods for production and use
CA2768239A1 (en) 2009-07-16 2011-01-20 Abbott Laboratories Processes for the synthesis of (2s, 3ar, 7as)-octahydro-1h-indole carboxylic acid as an intermediate for trandolapril
CN109689611B (zh) 2016-07-21 2021-09-28 株式会社钟化 有机化合物的制造方法

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
NZ202903A (en) * 1981-12-29 1988-01-08 Hoechst Ag 1-- pe pyrrol-2-yl-carboxylic acid derivatives and pharmaceutical compositions
JPS6248696A (ja) * 1985-08-27 1987-03-03 Kanegafuchi Chem Ind Co Ltd N−〔1(s)−エトキシカルボニル−3−フエニルプロピル〕−l−アラニル−l−プロリンの製造法
US6541635B1 (en) * 2002-03-29 2003-04-01 Everlight Usa, Inc. Method for producing angiotensin converting enzyme inhibitor

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