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MXPA03010394A - Proceso para la preparacion de esteres de acido carboxilico substituidos por hidrolisis enzimatica. - Google Patents

Proceso para la preparacion de esteres de acido carboxilico substituidos por hidrolisis enzimatica.

Info

Publication number
MXPA03010394A
MXPA03010394A MXPA03010394A MXPA03010394A MXPA03010394A MX PA03010394 A MXPA03010394 A MX PA03010394A MX PA03010394 A MXPA03010394 A MX PA03010394A MX PA03010394 A MXPA03010394 A MX PA03010394A MX PA03010394 A MXPA03010394 A MX PA03010394A
Authority
MX
Mexico
Prior art keywords
halogenpent
alkyl
carboxylic esters
ene carboxylic
preparation
Prior art date
Application number
MXPA03010394A
Other languages
English (en)
Inventor
Stutz Stefan
Original Assignee
Speedel Pharma Ag
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 Speedel Pharma Ag filed Critical Speedel Pharma Ag
Publication of MXPA03010394A publication Critical patent/MXPA03010394A/es

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12PFERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
    • C12P7/00Preparation of oxygen-containing organic compounds
    • C12P7/62Carboxylic acid esters
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12PFERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
    • C12P41/00Processes using enzymes or microorganisms to separate optical isomers from a racemic mixture
    • C12P41/003Processes using enzymes or microorganisms to separate optical isomers from a racemic mixture by ester formation, lactone formation or the inverse reactions
    • C12P41/005Processes using enzymes or microorganisms to separate optical isomers from a racemic mixture by ester formation, lactone formation or the inverse reactions by esterification of carboxylic acid groups in the enantiomers or the inverse reaction

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Zoology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Wood Science & Technology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Microbiology (AREA)
  • General Chemical & Material Sciences (AREA)
  • Biotechnology (AREA)
  • Health & Medical Sciences (AREA)
  • Biochemistry (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • General Engineering & Computer Science (AREA)
  • General Health & Medical Sciences (AREA)
  • Genetics & Genomics (AREA)
  • Analytical Chemistry (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Preparation Of Compounds By Using Micro-Organisms (AREA)

Abstract

Un proceso para la preparacion de esteres 2(S)-alquil-5-halogenpent-4-en carboxilicos por hidrolisis enzimatica, que comprende las etapas de a) hidrolisis enzimatica de esteres 2-alquil-5-halogenpent-4-en carboxilicos racemicos en medio acuoso y alcalino en la presencia de una esterasa; b ) aislamiento de esteres 2 ( S ) -alquil-5-halogenpent-4-en carboxilicos por extraccih con un solvente organico; c) aislamiento de acidos 2(R)-alquil-5-halogenpent-4-en carboxilicos del medio acuoso-alcalino; d) esterificacion de acidos 2 (R) -alquil-5- halogenpent-4-en carboxilicos, e) subsecuente racemizacion para formar esteres 2-alquil-5-halogenpent-4-en carboxilicos; y f ) regreso del racernato obtenido en la etapa e) a etapa a) , de ser necesario, junto con esteres 2-alquil-5-halogenpent-4-en carboxilicos racemicos frescos. El proceso permite que los R-estereois6meros indeseados se conviertan en loa esteres 2(S)-alquil-5-halogenpent-4-en carboxilicos deseados para evitar producto de desecho de la sintesis.
MXPA03010394A 2001-05-15 2002-04-26 Proceso para la preparacion de esteres de acido carboxilico substituidos por hidrolisis enzimatica. MXPA03010394A (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
CH8952001 2001-05-15
PCT/EP2002/004640 WO2002092828A2 (en) 2001-05-15 2002-04-26 Process for the preparation of substituted carboxylic acid estersby enzymatic hydrolysis

Publications (1)

Publication Number Publication Date
MXPA03010394A true MXPA03010394A (es) 2004-03-09

Family

ID=4546156

Family Applications (1)

Application Number Title Priority Date Filing Date
MXPA03010394A MXPA03010394A (es) 2001-05-15 2002-04-26 Proceso para la preparacion de esteres de acido carboxilico substituidos por hidrolisis enzimatica.

Country Status (14)

Country Link
US (1) US7153675B2 (es)
EP (1) EP1412514B1 (es)
JP (1) JP4252803B2 (es)
KR (1) KR100897597B1 (es)
CN (1) CN1279178C (es)
AT (1) ATE458066T1 (es)
AU (1) AU2002310883A1 (es)
BR (1) BR0209657B1 (es)
CA (1) CA2445014C (es)
DE (1) DE60235374D1 (es)
IL (2) IL158586A0 (es)
MX (1) MXPA03010394A (es)
PT (1) PT1412514E (es)
WO (1) WO2002092828A2 (es)

Families Citing this family (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2004052828A1 (ja) * 2002-12-09 2004-06-24 Asahi Glass Company, Limited (4e)−5−クロロ−2−イソプロピル−4−ペンテン酸エステルおよびその光学活性体の製造方法
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
US20080281125A1 (en) * 2005-03-09 2008-11-13 Markus Rossler Process for Preparing Enantiopure E-(2S)-Alkyl-5-Halopent-4-Enoic Acids and Esters
DE102005052195A1 (de) 2005-10-28 2007-05-03 Reuter Chemischer Apparatebau Kg Verfahren zur Herstellung von chiralen Octensäurederivaten
AT502992B1 (de) * 2005-12-27 2008-04-15 Dsm Fine Chem Austria Gmbh Verfahren zur herstellung von enantiomerenangereicherten 2-alkyl-5-halogen-pent-4-en-carbonsäuren bzw. -carbonsäureestern
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
WO2011051853A1 (en) 2009-10-29 2011-05-05 CarboDesign LLC Manufacturing process for preparing enaniomerically pure 8- aryloctanoic acid derivatives such as aliskiren
US8703976B2 (en) 2011-10-02 2014-04-22 Milan Soukup Manufacturing process for 8-aryloctanoic acids such as Aliskiren

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
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
US5658796A (en) 1995-06-07 1997-08-19 Seprachem, Inc. Optical resolution of alkyl chroman-2-carboxylates
DE19809649A1 (de) 1998-03-06 1999-09-09 Hoechst Marion Roussel De Gmbh Verfahren zur enzymatischen Enantiomeren-Trennung von 3(R)- und 3(S)-Hydroxy-1-methyl-4-(2,4,6-trimethoxyphenyl)-1,2,3,6-tetrahydro-pyridin bzw. der Carbonsäureester
AU5518500A (en) * 1999-07-29 2001-02-19 Speedel Pharma Ag 2-alkyl-5-halogen-pent-4-ene carboxylic acids and their production

Also Published As

Publication number Publication date
BR0209657B1 (pt) 2014-10-21
US7153675B2 (en) 2006-12-26
JP2004524860A (ja) 2004-08-19
CN1520461A (zh) 2004-08-11
IL158586A (en) 2008-08-07
JP4252803B2 (ja) 2009-04-08
CA2445014C (en) 2011-10-11
PT1412514E (pt) 2010-04-27
US20040132148A1 (en) 2004-07-08
DE60235374D1 (de) 2010-04-01
KR100897597B1 (ko) 2009-05-14
WO2002092828A3 (en) 2004-02-26
CN1279178C (zh) 2006-10-11
BR0209657A (pt) 2004-04-20
ATE458066T1 (de) 2010-03-15
EP1412514B1 (en) 2010-02-17
IL158586A0 (en) 2004-05-12
KR20040026655A (ko) 2004-03-31
WO2002092828A2 (en) 2002-11-21
EP1412514A2 (en) 2004-04-28
WO2002092828A9 (en) 2004-05-06
AU2002310883A1 (en) 2002-11-25
CA2445014A1 (en) 2002-11-21

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