RU2012103753A - Способ синтеза (2s, 3ar, 7as)-октагидро-1н-индол-карбоновой кислоты в качестве промежуточного соединения для получения трандолаприла - Google Patents

Способ синтеза (2s, 3ar, 7as)-октагидро-1н-индол-карбоновой кислоты в качестве промежуточного соединения для получения трандолаприла Download PDF

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Publication number
RU2012103753A
RU2012103753A RU2012103753/04A RU2012103753A RU2012103753A RU 2012103753 A RU2012103753 A RU 2012103753A RU 2012103753/04 A RU2012103753/04 A RU 2012103753/04A RU 2012103753 A RU2012103753 A RU 2012103753A RU 2012103753 A RU2012103753 A RU 2012103753A
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RU
Russia
Prior art keywords
ethyl
phenylethylamino
compound
formula
indole
Prior art date
Application number
RU2012103753/04A
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English (en)
Russian (ru)
Inventor
Санджай Р. Чембуркар
Раджаратнам И. РЕДДИ
Дуглас М. РИМЕР
Джон Т. ПАВЛИНА
Стефен С. УЛРЕЙ
Брайен Дж. КОТЕЦКИ
Original Assignee
Эбботт Лабораториз
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.)
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Publication date
Application filed by Эбботт Лабораториз filed Critical Эбботт Лабораториз
Publication of RU2012103753A publication Critical patent/RU2012103753A/ru

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Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
    • C07D209/04—Indoles; Hydrogenated indoles
    • C07D209/30—Indoles; Hydrogenated indoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to carbon atoms of the hetero ring
    • C07D209/42—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Cardiology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Indole Compounds (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
RU2012103753/04A 2009-07-16 2010-07-16 Способ синтеза (2s, 3ar, 7as)-октагидро-1н-индол-карбоновой кислоты в качестве промежуточного соединения для получения трандолаприла RU2012103753A (ru)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US22603009P 2009-07-16 2009-07-16
US61/226,030 2009-07-16
PCT/US2010/042219 WO2011009021A1 (en) 2009-07-16 2010-07-16 Processes for the synthesis of (2s, 3ar, 7as)-octahydro-1h-indole carboxylic acid as an intermediate for trandolapril

Publications (1)

Publication Number Publication Date
RU2012103753A true RU2012103753A (ru) 2013-08-27

Family

ID=42585097

Family Applications (1)

Application Number Title Priority Date Filing Date
RU2012103753/04A RU2012103753A (ru) 2009-07-16 2010-07-16 Способ синтеза (2s, 3ar, 7as)-октагидро-1н-индол-карбоновой кислоты в качестве промежуточного соединения для получения трандолаприла

Country Status (10)

Country Link
US (1) US8288565B2 (cg-RX-API-DMAC7.html)
EP (1) EP2454235A1 (cg-RX-API-DMAC7.html)
JP (1) JP2012533563A (cg-RX-API-DMAC7.html)
CN (1) CN102498098A (cg-RX-API-DMAC7.html)
AU (1) AU2010273259B2 (cg-RX-API-DMAC7.html)
CA (1) CA2768239A1 (cg-RX-API-DMAC7.html)
CO (1) CO6491043A2 (cg-RX-API-DMAC7.html)
IN (1) IN2012DN00453A (cg-RX-API-DMAC7.html)
RU (1) RU2012103753A (cg-RX-API-DMAC7.html)
WO (1) WO2011009021A1 (cg-RX-API-DMAC7.html)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN111620788B (zh) * 2020-04-20 2022-09-30 广东莱佛士制药技术有限公司 一种制备(2s,3s)-3-氨基-二环[2.2.2]辛烷-2-甲酸酯的方法

Family Cites Families (18)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US487932A (en) 1892-12-13 George b
US4350704A (en) 1980-10-06 1982-09-21 Warner-Lambert Company Substituted acyl derivatives of octahydro-1H-indole-2-carboxylic acids
GR78413B (cg-RX-API-DMAC7.html) 1981-12-29 1984-09-27 Hoechst Ag
US4490386A (en) * 1982-09-23 1984-12-25 Warner-Lambert Company Phosphate salts of 1-[2-[(1-alkoxycarbonyl-3-aralkyl)-amino]-1-oxoalkyl]octahydro-1H-indole-2-carboxylic acids, preparation of, and medical compositions thereof
US4556655A (en) 1984-09-24 1985-12-03 Schering Corporation Antihypertensive compounds having both diuretic and angiotensin converting enzyme inhibitory activity
FR2605630B1 (fr) * 1986-10-22 1989-06-30 Roussel Uclaf Procede de preparation de derives de l'octahydroindole et intermediaires de preparation
DE19900205A1 (de) 1999-01-07 2000-07-13 Basf Ag Verfahren zur Herstellung von (2S,4R,9S)-Octahydro-1H-indol-2-carbonsäure und Zwischenprodukte dafür
WO2004065368A1 (ja) 2003-01-21 2004-08-05 Ohara Chemical Industries, Ltd. トランドラプリル合成中間体の製造方法
ES2233913T3 (es) * 2003-04-15 2005-06-16 Les Laboratoires Servier Nuevo procedimiento de sintesis del acido (2s,3as,7as) perhidroindol-2-carboxilico y de sus esteres, y aplicacion as la sintesis de perindopril.
SI21507A (sl) 2003-05-16 2004-12-31 LEK farmacevtska dru�ba d.d. Postopek za pripravo spojin z ace inhibitornim delovanjem
EP1687271A1 (en) * 2003-11-25 2006-08-09 Texcontor Etablissement A method for the preparation of (2s, 3ar, 7as)-octahydro-1h-indole-2-carboxylic acid as key intermediate in the preparation of trandolapril by reacting a cyclohexyl aziridine with a dialkyl malonate
US20070135513A1 (en) 2003-11-28 2007-06-14 Mirko Pogutter Method for producing {n-[1-(s)-carbalkoxy-3-phenylpropyl]-s-alanyl-2s, 3ar, 7as-octahydroindole-2-carboxylic acid} compounds
WO2006014916A2 (en) 2004-07-26 2006-02-09 Dr. Reddy's Laboratories Ltd. Preparation of trandolapril
US20080171885A1 (en) 2005-02-14 2008-07-17 Lupin Limited Process for Preparation of Highly Pure Trandolapril
EP1724260B1 (en) 2005-05-06 2008-02-20 Sochinaz SA Process for the synthesis of (2S, 3aR, 7aS)octahydroindole-2-carboxylic acid and its conversion to trandolapril
KR20080046630A (ko) 2005-07-05 2008-05-27 씨아이피엘에이 엘티디. Ａｃｅ 저해제 트란돌라프릴의 제조방법
US8536198B2 (en) 2007-07-24 2013-09-17 Bristol-Myers Squibb Company Piperidine derivatives as modulators of chemokine receptor activity
CN101423490B (zh) * 2008-06-16 2012-07-18 重庆南松医药科技股份有限公司 群多普利关键中间体（2S,3aR,7as）-八氢－1H－吲哚－2－羧酸的合成方法

Also Published As

Publication number Publication date
AU2010273259B2 (en) 2013-03-07
CN102498098A (zh) 2012-06-13
CA2768239A1 (en) 2011-01-20
CO6491043A2 (es) 2012-07-31
IN2012DN00453A (cg-RX-API-DMAC7.html) 2015-05-15
JP2012533563A (ja) 2012-12-27
AU2010273259A1 (en) 2012-02-09
US8288565B2 (en) 2012-10-16
WO2011009021A1 (en) 2011-01-20
EP2454235A1 (en) 2012-05-23
US20110065930A1 (en) 2011-03-17

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Effective date: 20140901