EP4103168A4 - Procédé de préparation d'acides gamma-amino-butyriques et de leurs analogues - Google Patents

Procédé de préparation d'acides gamma-amino-butyriques et de leurs analogues Download PDF

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Publication number
EP4103168A4
EP4103168A4 EP21753915.4A EP21753915A EP4103168A4 EP 4103168 A4 EP4103168 A4 EP 4103168A4 EP 21753915 A EP21753915 A EP 21753915A EP 4103168 A4 EP4103168 A4 EP 4103168A4
Authority
EP
European Patent Office
Prior art keywords
aminobutry
analogues
gamma
acids
production
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.)
Pending
Application number
EP21753915.4A
Other languages
German (de)
English (en)
Other versions
EP4103168A1 (fr
Inventor
Chada Raji REDDY
Amol Dnyandev PATIL
Muppidi SUBBARAO
Bodasu SRINIVAS
Genji SUKUMAR
Srivari CHANDRASEKHAR
Thennati Rajamannar
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.)
Council of Scientific and Industrial Research CSIR
Original Assignee
Council of Scientific and Industrial Research CSIR
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 Council of Scientific and Industrial Research CSIR filed Critical Council of Scientific and Industrial Research CSIR
Publication of EP4103168A1 publication Critical patent/EP4103168A1/fr
Publication of EP4103168A4 publication Critical patent/EP4103168A4/fr
Pending legal-status Critical Current

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Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C249/00Preparation of compounds containing nitrogen atoms doubly-bound to a carbon skeleton
    • C07C249/04Preparation of compounds containing nitrogen atoms doubly-bound to a carbon skeleton of oximes
    • C07C249/08Preparation of compounds containing nitrogen atoms doubly-bound to a carbon skeleton of oximes by reaction of hydroxylamines with carbonyl compounds
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C227/00Preparation of compounds containing amino and carboxyl groups bound to the same carbon skeleton
    • C07C227/14Preparation of compounds containing amino and carboxyl groups bound to the same carbon skeleton from compounds containing already amino and carboxyl groups or derivatives thereof
    • C07C227/18Preparation of compounds containing amino and carboxyl groups bound to the same carbon skeleton from compounds containing already amino and carboxyl groups or derivatives thereof by reactions involving amino or carboxyl groups, e.g. hydrolysis of esters or amides, by formation of halides, salts or esters
    • C07C227/20Preparation of compounds containing amino and carboxyl groups bound to the same carbon skeleton from compounds containing already amino and carboxyl groups or derivatives thereof by reactions involving amino or carboxyl groups, e.g. hydrolysis of esters or amides, by formation of halides, salts or esters by hydrolysis of N-acylated amino-acids or derivatives thereof, e.g. hydrolysis of carbamates
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C231/00Preparation of carboxylic acid amides
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C67/00Preparation of carboxylic acid esters
    • C07C67/30Preparation of carboxylic acid esters by modifying the acid moiety of the ester, such modification not being an introduction of an ester group
    • C07C67/333Preparation of carboxylic acid esters by modifying the acid moiety of the ester, such modification not being an introduction of an ester group by isomerisation; by change of size of the carbon skeleton
    • C07C67/343Preparation of carboxylic acid esters by modifying the acid moiety of the ester, such modification not being an introduction of an ester group by isomerisation; by change of size of the carbon skeleton by increase in the number of carbon atoms
    • C07C67/347Preparation of carboxylic acid esters by modifying the acid moiety of the ester, such modification not being an introduction of an ester group by isomerisation; by change of size of the carbon skeleton by increase in the number of carbon atoms by addition to unsaturated carbon-to-carbon bonds

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
EP21753915.4A 2020-02-14 2021-02-13 Procédé de préparation d'acides gamma-amino-butyriques et de leurs analogues Pending EP4103168A4 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
IN202011006475 2020-02-14
PCT/IN2021/050141 WO2021161346A1 (fr) 2020-02-14 2021-02-13 Procédé de préparation d'acides gamma-amino-butyriques et de leurs analogues

Publications (2)

Publication Number Publication Date
EP4103168A1 EP4103168A1 (fr) 2022-12-21
EP4103168A4 true EP4103168A4 (fr) 2024-04-24

Family

ID=77293016

Family Applications (1)

Application Number Title Priority Date Filing Date
EP21753915.4A Pending EP4103168A4 (fr) 2020-02-14 2021-02-13 Procédé de préparation d'acides gamma-amino-butyriques et de leurs analogues

Country Status (3)

Country Link
EP (1) EP4103168A4 (fr)
JP (1) JP7436689B2 (fr)
WO (1) WO2021161346A1 (fr)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN116655482B (zh) * 2023-06-05 2024-06-04 贵州大学 一类γ-氨基丁酸衍生物的制备方法

Family Cites Families (19)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5072023A (en) * 1990-02-15 1991-12-10 E. R. Squibb & Sons, Inc. Process for preparing highly substituted phenyls
US6197819B1 (en) 1990-11-27 2001-03-06 Northwestern University Gamma amino butyric acid analogs and optical isomers
US5616793A (en) 1995-06-02 1997-04-01 Warner-Lambert Company Methods of making (S)-3-(aminomethyl)-5-methylhexanoic acid
JP2002241358A (ja) * 2001-02-15 2002-08-28 Nippon Soda Co Ltd オキシム基を有する化合物及び殺虫・殺ダニ剤
JP4250887B2 (ja) * 2001-10-22 2009-04-08 三菱化学株式会社 アミド化合物の製造方法
JP4562370B2 (ja) * 2003-10-02 2010-10-13 独立行政法人科学技術振興機構 転位不飽和化合物の製造方法
HRP20100054T1 (hr) * 2004-06-21 2010-05-31 Warner-Lambert Company Llc Dobivanje pregabalina i njemu sličnih spojeva
EP1768950A2 (fr) * 2005-04-11 2007-04-04 Teva Pharmaceutical Industries Ltd. Procede de fabrication de (s)-pregabaline
WO2007066828A1 (fr) * 2005-12-09 2007-06-14 Sumitomo Chemical Company, Limited Procede de fabrication d’acide phenylbutanoique 4-amino-3-substitue optiquement actif
WO2008062460A2 (fr) * 2006-10-06 2008-05-29 Cadila Healthcare Limited Formes cristallines de la prégabaline
KR20090101462A (ko) 2007-10-03 2009-09-28 테바 파마슈티컬 인더스트리즈 리미티드 프레가발린-4-엘리미네이트, 프레가발린 5-엘리미네이트, 기준 마커 및 표준물로서의 이들의 용도, 및 이들을 낮은 수준으로 함유하는 프레가발린의 제조 방법
WO2009125427A2 (fr) 2008-02-18 2009-10-15 Matrix Laboratories Limited Procédé de fabrication d'acide (s)-3-(aminométhyl)-5-méthylhexanoïque
EP2294207B1 (fr) * 2008-05-21 2012-09-26 Sandoz AG Procédé pour l'hydrolyse enzymatique stéréosélective d'un ester d'acide 5-méthyl-3-nitrométhyl-hexanoïque
WO2010061403A2 (fr) * 2008-11-26 2010-06-03 Ind-Swift Laboratories Limited Procédé pour préparer de la (s)-prégabaline très pure
WO2012093411A2 (fr) * 2011-01-07 2012-07-12 Dr Braja Sundar Pradhan Méthode de préparation d'acide r-(-)-3-(carbamoylméthyl)-5-méthylhexanoïque et de ses intermédiaires
WO2014072785A2 (fr) * 2012-11-07 2014-05-15 Hikal Limited Procédé de préparation de prégabaline
US9422230B2 (en) 2013-05-09 2016-08-23 Council Of Scientific And Industrial Research Process for the preparation of an anticonvulsant agent pregabalin hydrochloride
CN103833562B (zh) 2013-12-04 2015-08-12 惠州市莱佛士制药技术有限公司 一种不对称合成普瑞巴林的制备方法
JP6724283B2 (ja) * 2016-03-09 2020-07-15 国立大学法人 東京大学 光学活性の4−ニトロブタン酸エステル及びプレガバリンの製造方法

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
H. ISHITANI, ET AL.: "Synthesis of (+/- )-pregabalin by utilising a three-step sequential-flow system with heterogeneous catalysts", EUROPEAN JOURNAL OF ORGANIC CHEMISTRY, vol. 2017, no. 44, 10 October 2017 (2017-10-10), Wiley-VCH Verlag, Weinheim, DE, pages 6491 - 6494, XP072119280, ISSN: 1434-193X, DOI: 10.1002/ejoc.201700998 *

Also Published As

Publication number Publication date
EP4103168A1 (fr) 2022-12-21
WO2021161346A1 (fr) 2021-08-19
JP7436689B2 (ja) 2024-02-22
JP2023513330A (ja) 2023-03-30

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