JP2003506347A5 - - Google Patents

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Publication number
JP2003506347A5
JP2003506347A5 JP2001514287A JP2001514287A JP2003506347A5 JP 2003506347 A5 JP2003506347 A5 JP 2003506347A5 JP 2001514287 A JP2001514287 A JP 2001514287A JP 2001514287 A JP2001514287 A JP 2001514287A JP 2003506347 A5 JP2003506347 A5 JP 2003506347A5
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JP
Japan
Prior art keywords
alkyl
formula
compound
methoxy
alkoxy
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.)
Granted
Application number
JP2001514287A
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English (en)
Japanese (ja)
Other versions
JP2003506347A (ja
JP4922521B2 (ja
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Publication date
Application filed filed Critical
Priority claimed from PCT/CH2000/000384 external-priority patent/WO2001009083A1/de
Publication of JP2003506347A publication Critical patent/JP2003506347A/ja
Publication of JP2003506347A5 publication Critical patent/JP2003506347A5/ja
Application granted granted Critical
Publication of JP4922521B2 publication Critical patent/JP4922521B2/ja
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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JP2001514287A 1999-07-29 2000-07-13 N−置換2,7−ジアルキル−4−ヒドロキシ−5−アミノ−8−アリール−オクタノイルアミドの製造 Expired - Fee Related JP4922521B2 (ja)

Applications Claiming Priority (5)

Application Number Priority Date Filing Date Title
CH140199 1999-07-29
CH1401/99 1999-07-29
CH44/00 2000-01-11
CH442000 2000-01-11
PCT/CH2000/000384 WO2001009083A1 (de) 1999-07-29 2000-07-13 Herstellung von n-substituierten 2,7-dialkyl-4-hydroxy-5-amino-8-aryl-octanoylamiden

Publications (3)

Publication Number Publication Date
JP2003506347A JP2003506347A (ja) 2003-02-18
JP2003506347A5 true JP2003506347A5 (https=) 2007-08-02
JP4922521B2 JP4922521B2 (ja) 2012-04-25

Family

ID=25687539

Family Applications (2)

Application Number Title Priority Date Filing Date
JP2001514283A Expired - Lifetime JP4580606B2 (ja) 1999-07-29 2000-07-13 2−アルキル−5−ハロゲノ−ペンタ−4−エンカルボン酸およびそれの製造
JP2001514287A Expired - Fee Related JP4922521B2 (ja) 1999-07-29 2000-07-13 N−置換2,7−ジアルキル−4−ヒドロキシ−5−アミノ−8−アリール−オクタノイルアミドの製造

Family Applications Before (1)

Application Number Title Priority Date Filing Date
JP2001514283A Expired - Lifetime JP4580606B2 (ja) 1999-07-29 2000-07-13 2−アルキル−5−ハロゲノ−ペンタ−4−エンカルボン酸およびそれの製造

Country Status (10)

Country Link
US (3) US6777574B1 (https=)
EP (2) EP1200390B1 (https=)
JP (2) JP4580606B2 (https=)
AT (2) ATE406346T1 (https=)
AU (2) AU5518400A (https=)
DE (2) DE50006271D1 (https=)
DK (2) DK1200390T3 (https=)
ES (2) ES2312346T3 (https=)
PT (2) PT1200390E (https=)
WO (2) WO2001009079A1 (https=)

Families Citing this family (39)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AU7376301A (en) 2000-07-05 2002-01-14 Speedel Pharma Ag Process for the preparation of substituted octanoyl amides
IL158586A0 (en) 2001-05-15 2004-05-12 Speedel Pharma Ag Process for the preparation of substituted carboxylic acid esters by enzymatic hydrolysis
US20060154926A1 (en) * 2002-06-11 2006-07-13 Elan Pharmaceuticals, Inc. Methods of treating alzheimer's disease using aryl alkanoic acid amides
DE60312214T3 (de) 2002-12-09 2015-02-26 Asahi Glass Co., Ltd. Verfahren zur herstellung von(4e)-5-chloro-2-isopropyl-4-pentensäureester und optischaktivem isomer davon
EP1626093A1 (en) * 2004-08-11 2006-02-15 Dow Global Technologies Inc. Process for the production of (S)-5-chloro-2-isopropylpent-4-enoic acid esters
WO2006099926A1 (en) * 2005-03-09 2006-09-28 Dsm Fine Chemicals Austria Nfg Gmbh & Co Kg Process for preparing enantiopure e-(2s)-alkyl-5-halopent-4-enoic acids and esters
JP4763771B2 (ja) * 2005-03-17 2011-08-31 ビーエーエスエフ ソシエタス・ヨーロピア 光学活性3−フェニルプロピオン酸誘導体を生成する方法、およびその誘導体の後続生成物
WO2006117057A1 (en) * 2005-05-02 2006-11-09 Dsm Fine Chemicals Austria Nfg Gmbh & Co Kg Process for preparing enantiomerically enriched e-(2s)- and (2r)-alkyl-5-halopent-4-enecarboxylic acids or their esters
AT502257B1 (de) * 2005-07-25 2007-04-15 Dsm Fine Chem Austria Gmbh Verfahren zur herstellung von racemischen alkyl-5-halogen-pent-4-en-carbonsäuren bzw. -carbonsäureestern
DE102005042458A1 (de) * 2005-09-06 2007-03-22 Basf Ag Verfahren zur Herstellung von 2-substituierten Carbonsäuren
WO2007036491A1 (de) * 2005-09-30 2007-04-05 Basf Aktiengesellschaft Verfahren zur herstellung von alpha-substituierten carbonsäuren
GB0521083D0 (en) 2005-10-17 2005-11-23 Novartis Ag Organic compounds
GB2431640A (en) * 2005-10-25 2007-05-02 Novartis Ag Alternative synthesis of aryl-octanoyl amide compounds
GB2431654A (en) * 2005-10-25 2007-05-02 Novartis Ag Alternative synthesis of aryl-octanoyl amide compounds
DE102005052195A1 (de) 2005-10-28 2007-05-03 Reuter Chemischer Apparatebau Kg Verfahren zur Herstellung von chiralen Octensäurederivaten
WO2007069745A1 (ja) * 2005-12-16 2007-06-21 Asahi Glass Company, Limited 光学活性な(4e)-5-クロロ-2-イソプロピル-4-ペンテン酸またはその塩基性アミノ酸塩の製造方法
TW200837046A (en) * 2006-11-08 2008-09-16 Speedel Experimenta Ag Process for preparing organic compounds
EP1958666A1 (en) 2007-02-13 2008-08-20 Speedel Experimenta AG Heterocyclic-substituted alkanamides as therapeutic compounds
DE102007049039A1 (de) 2007-10-11 2009-04-16 Reuter Chemischer Apparatebau Kg Verfahren zur Herstellung von 8-Hydrazino-8-Aryl-Octanoylderivaten und deren Verwendung
EP2062874B1 (en) 2007-11-20 2014-12-17 KRKA, tovarna zdravil, d.d., Novo mesto Process and intermediates for the preparation of aliskiren
EP2225200B1 (en) * 2007-12-24 2013-10-16 DSM IP Assets B.V. Convergent synthesis of renin inhibitors and intermediates useful therein
US20100029774A1 (en) * 2008-05-23 2010-02-04 Nina Finkelstein Aliskiren monofumarate and processes for preparation thereof
SI2189442T1 (sl) 2008-11-20 2015-03-31 Krka, Tovarna Zdravil, D.D., Novo Mesto Postopek in intermediati za pripravo aliskirena
EA201190091A1 (ru) 2009-02-05 2012-01-30 Крка, Товарна Здравил, Д. Д., Ново Место Активируемый влагой способ грануляции
US8203005B2 (en) 2009-10-29 2012-06-19 Carbo Design Llc Manufacturing process for enantiomerically pure 8-aryloctanoic acids as Aliskiren
CN101774986B (zh) 2010-01-06 2012-03-28 浙江天宇药业股份有限公司 一种制备阿利克伦及其中间体的方法
TR201002256A1 (tr) 2010-03-24 2011-10-21 Sanovel �La� Sanay� Ve T�Caret Anon�M ��Rket� Stabil aliskiren formülasyonları
US20110268797A1 (en) 2010-04-30 2011-11-03 Sanovel IIac Sanayi Ve Ticaret Anonim Sirketi Multicoated aliskiren formulations
PT2630118E (pt) 2010-10-19 2015-02-10 Mylan Lab Ltd Síntese do aliskiren
US8703976B2 (en) 2011-10-02 2014-04-22 Milan Soukup Manufacturing process for 8-aryloctanoic acids such as Aliskiren
WO2013118138A1 (en) 2011-12-13 2013-08-15 Laboratories Ltd Mylan Novel process for the preparation of renin inhibitors
EP2814806B1 (en) 2012-02-17 2016-05-25 Mylan Laboratories Ltd. An improved process for the preparation of aliskiren
WO2013124868A2 (en) 2012-02-21 2013-08-29 Mylan Laboratories Limited Solid form of aliskiren intermediate
WO2013144979A1 (en) 2012-03-28 2013-10-03 Maylan Laboratories Ltd Process for the preparation of aliskiren
WO2013171767A1 (en) 2012-05-18 2013-11-21 Mylan Laboratories Limited An improved process for the preparation of aliskiren
CN103130677B (zh) * 2013-03-12 2015-01-07 博瑞生物医药技术(苏州)有限公司 一种阿利克仑的制备方法
WO2014207206A1 (en) * 2013-06-27 2014-12-31 Dpx Holdings B.V. Preparation of grignard reagents using a fluidized bed
CN103351300A (zh) * 2013-06-30 2013-10-16 北京万全德众医药生物技术有限公司 一种制备阿利克仑中间体侧链(s)-2-溴代异戊酸甲酯的方法
CN105294478B (zh) * 2014-07-01 2017-06-13 华润双鹤药业股份有限公司 阿利吉仑的一种非对映异构体、其制备方法及用途

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4492799A (en) * 1979-07-02 1985-01-08 Union Carbide Corporation Halo-4-alkenoic acids and their use as pesticidal intermediates
US4291057A (en) * 1979-07-02 1981-09-22 Union Carbide Corporation Biocidal esters of halo-4-alkenoic acids
MY119161A (en) * 1994-04-18 2005-04-30 Novartis Ag Delta-amino-gamma-hydroxy-omega-aryl-alkanoic acid amides with enzyme especially renin inhibiting activities
CA2247580A1 (en) * 1997-10-03 1999-04-03 F. Hoffmann-La Roche Ag Process for preparing chiral succinic acid derivatives

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