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NO20062599L - Fremgangsmate for syntese av perindopril og farmasoytisk akseptable salter derav - Google Patents

Fremgangsmate for syntese av perindopril og farmasoytisk akseptable salter derav

Info

Publication number
NO20062599L
NO20062599L NO20062599A NO20062599A NO20062599L NO 20062599 L NO20062599 L NO 20062599L NO 20062599 A NO20062599 A NO 20062599A NO 20062599 A NO20062599 A NO 20062599A NO 20062599 L NO20062599 L NO 20062599L
Authority
NO
Norway
Prior art keywords
perindopril
synthesis
pharmaceutically acceptable
acceptable salts
formula
Prior art date
Application number
NO20062599A
Other languages
English (en)
Other versions
NO336349B1 (no
Inventor
Pascal Langlois
Thierry Dubuffet
Original Assignee
Servier Lab
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 Servier Lab filed Critical Servier Lab
Publication of NO20062599L publication Critical patent/NO20062599L/no
Publication of NO336349B1 publication Critical patent/NO336349B1/no

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K5/00Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
    • C07K5/04Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
    • C07K5/06Dipeptides
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K5/00Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
    • C07K5/04Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
    • C07K5/06Dipeptides
    • C07K5/06008Dipeptides with the first amino acid being neutral
    • C07K5/06017Dipeptides with the first amino acid being neutral and aliphatic
    • C07K5/06026Dipeptides with the first amino acid being neutral and aliphatic the side chain containing 0 or 1 carbon atom, i.e. Gly or Ala
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • A61P9/04Inotropic agents, i.e. stimulants of cardiac contraction; Drugs for heart failure
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • A61P9/12Antihypertensives
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C229/00Compounds containing amino and carboxyl groups bound to the same carbon skeleton
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C233/00Carboxylic acid amides
    • C07C233/01Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms
    • C07C233/45Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by carboxyl groups
    • C07C233/46Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by carboxyl groups with the substituted hydrocarbon radical bound to the nitrogen atom of the carboxamide group by an acyclic carbon atom
    • C07C233/47Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by carboxyl groups with the substituted hydrocarbon radical bound to the nitrogen atom of the carboxamide group by an acyclic carbon atom having the carbon atom of the carboxamide group bound to a hydrogen atom or to a carbon atom of an acyclic saturated carbon skeleton
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C309/00Sulfonic acids; Halides, esters, or anhydrides thereof
    • C07C309/63Esters of sulfonic acids
    • C07C309/72Esters of sulfonic acids having sulfur atoms of esterified sulfo groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton
    • C07C309/73Esters of sulfonic acids having sulfur atoms of esterified sulfo groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton to carbon atoms of non-condensed six-membered aromatic rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K5/00Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02PCLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P20/00Technologies relating to chemical industry
    • Y02P20/50Improvements relating to the production of bulk chemicals
    • Y02P20/55Design of synthesis routes, e.g. reducing the use of auxiliary or protecting groups

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Molecular Biology (AREA)
  • Genetics & Genomics (AREA)
  • Proteomics, Peptides & Aminoacids (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Biophysics (AREA)
  • Biochemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Cardiology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Hospice & Palliative Care (AREA)
  • Indole Compounds (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Peptides Or Proteins (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Preparation Of Compounds By Using Micro-Organisms (AREA)

Abstract

Fremgangsmåte for syntesen av perindopril med formel (1) og farmasøytisk akseptable salter derav.
NO20062599A 2003-11-19 2006-06-06 Mellomproduktet og fremgangsmåte for syntese av perindopril og farmasøytisk akseptable salter derav NO336349B1 (no)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
EP03292864A EP1420028B1 (fr) 2003-11-19 2003-11-19 Pocédé de synthèse du perindopril et de ses sels pharmaceutiquement acceptables
PCT/FR2004/002936 WO2005054276A1 (fr) 2003-11-19 2004-11-18 Procede de synthese du perindopril et de ses sels pharmaceutiquement acceptables

Publications (2)

Publication Number Publication Date
NO20062599L true NO20062599L (no) 2006-06-06
NO336349B1 NO336349B1 (no) 2015-08-03

Family

ID=32116380

Family Applications (1)

Application Number Title Priority Date Filing Date
NO20062599A NO336349B1 (no) 2003-11-19 2006-06-06 Mellomproduktet og fremgangsmåte for syntese av perindopril og farmasøytisk akseptable salter derav

Country Status (28)

Country Link
US (1) US7208607B1 (no)
EP (1) EP1420028B1 (no)
JP (1) JP4377412B2 (no)
KR (1) KR100863394B1 (no)
CN (1) CN100447152C (no)
AR (1) AR047312A1 (no)
AT (1) ATE354586T1 (no)
AU (1) AU2004295132B2 (no)
BR (1) BRPI0416746B1 (no)
CA (1) CA2546506C (no)
CY (1) CY1106544T1 (no)
DE (1) DE60311942T2 (no)
DK (1) DK1420028T3 (no)
EA (1) EA010102B1 (no)
EG (1) EG26629A (no)
ES (1) ES2282586T3 (no)
GE (1) GEP20084547B (no)
MA (1) MA28144A1 (no)
MX (1) MXPA06005607A (no)
MY (1) MY138550A (no)
NO (1) NO336349B1 (no)
NZ (1) NZ546931A (no)
PL (1) PL210769B1 (no)
PT (1) PT1420028E (no)
SI (1) SI1420028T1 (no)
UA (1) UA83269C2 (no)
WO (1) WO2005054276A1 (no)
ZA (1) ZA200603675B (no)

Families Citing this family (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
SI1380591T1 (sl) * 2003-08-29 2006-02-28 Servier Lab Nov postopek sinteze perindoprila in njegovih farmacevtsko sprejemljivih soli
AU2004312530A1 (en) 2003-12-29 2005-07-21 Sepracor Inc. Pyrrole and pyrazole DAAO inhibitors
CN101553217A (zh) 2005-07-06 2009-10-07 塞普拉科公司 艾司佐匹克隆与反式4-(3,4-二氯苯基)-1,2,3,4-四氢-n-甲基-1-萘胺或反式4-(3,4-二氯苯基)-1,2,3,4-四氢-1-萘胺的组合以及治疗绝经期和心境障碍、焦虑症和认知障碍的方法
CA2636324C (en) 2006-01-06 2012-03-20 Sepracor Inc. Cycloalkylamines as monoamine reuptake inhibitors
US8053603B2 (en) 2006-01-06 2011-11-08 Sunovion Pharmaceuticals Inc. Tetralone-based monoamine reuptake inhibitors
AU2007233041B2 (en) 2006-03-31 2013-05-02 Sepracor Inc. Preparation of chiral amides and amines
US7884124B2 (en) 2006-06-30 2011-02-08 Sepracor Inc. Fluoro-substituted inhibitors of D-amino acid oxidase
US7902252B2 (en) 2007-01-18 2011-03-08 Sepracor, Inc. Inhibitors of D-amino acid oxidase
JP5420534B2 (ja) 2007-05-31 2014-02-19 サノビオン ファーマシューティカルズ インク モノアミン再取り込み阻害薬としてのフェニル置換シクロアルキルアミン
WO2016178591A2 (en) 2015-05-05 2016-11-10 Gene Predit, Sa Genetic markers and treatment of male obesity
PH12018502155B1 (en) 2016-04-20 2024-03-27 Servier Lab Pharmaceutical composition comprising a beta blocker, a converting enzyme inhibitor and an antihypertensive or an nsaid
CN112047869B (zh) * 2020-08-20 2021-12-21 华南理工大学 一种氮杂5,6-并环化合物的合成方法

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2620709B1 (fr) * 1987-09-17 1990-09-07 Adir Procede de synthese industrielle du perindopril et de ses principaux intermediaires de synthese

Also Published As

Publication number Publication date
DE60311942T2 (de) 2007-12-06
KR20060121202A (ko) 2006-11-28
BRPI0416746A (pt) 2007-01-16
MY138550A (en) 2009-06-30
CN100447152C (zh) 2008-12-31
BRPI0416746B1 (pt) 2018-02-14
JP2008502587A (ja) 2008-01-31
AR047312A1 (es) 2006-01-18
MXPA06005607A (es) 2006-08-17
HK1096689A1 (en) 2007-06-08
CA2546506C (fr) 2010-04-06
AU2004295132A1 (en) 2005-06-16
JP4377412B2 (ja) 2009-12-02
PL210769B1 (pl) 2012-02-29
EP1420028A3 (fr) 2004-05-26
KR100863394B1 (ko) 2008-10-14
WO2005054276A1 (fr) 2005-06-16
NO336349B1 (no) 2015-08-03
DK1420028T3 (da) 2007-06-18
ZA200603675B (en) 2007-09-26
EA010102B1 (ru) 2008-06-30
NZ546931A (en) 2010-01-29
GEP20084547B (en) 2008-11-25
EP1420028B1 (fr) 2007-02-21
ATE354586T1 (de) 2007-03-15
AU2004295132B2 (en) 2010-07-15
UA83269C2 (uk) 2008-06-25
CN1882607A (zh) 2006-12-20
US7208607B1 (en) 2007-04-24
PL380409A1 (pl) 2007-01-22
EG26629A (en) 2014-04-13
US20070083052A1 (en) 2007-04-12
ES2282586T3 (es) 2007-10-16
MA28144A1 (fr) 2006-09-01
SI1420028T1 (sl) 2007-06-30
PT1420028E (pt) 2007-05-31
EP1420028A2 (fr) 2004-05-19
CA2546506A1 (fr) 2005-06-16
CY1106544T1 (el) 2012-01-25
EA200600898A1 (ru) 2006-10-27
DE60311942D1 (de) 2007-04-05

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