HK1105215A1 - Stereoselective bioconversion of aliphatic dinitriles into cyano carboxylic acids - Google Patents

Stereoselective bioconversion of aliphatic dinitriles into cyano carboxylic acids

Info

Publication number
HK1105215A1
HK1105215A1 HK07110403.3A HK07110403A HK1105215A1 HK 1105215 A1 HK1105215 A1 HK 1105215A1 HK 07110403 A HK07110403 A HK 07110403A HK 1105215 A1 HK1105215 A1 HK 1105215A1
Authority
HK
Hong Kong
Prior art keywords
carboxylic acids
aliphatic dinitriles
cyano carboxylic
bioconversion
stereoselective
Prior art date
Application number
HK07110403.3A
Other languages
English (en)
Inventor
Michael Paul Burns
Justin Kaine Weaver
John Wing Wong
Original Assignee
Pfizer Prod Inc
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 Pfizer Prod Inc filed Critical Pfizer Prod Inc
Publication of HK1105215A1 publication Critical patent/HK1105215A1/xx

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
    • C12P7/00—Preparation of oxygen-containing organic compounds
    • C12P7/40—Preparation of oxygen-containing organic compounds containing a carboxyl group including Peroxycarboxylic acids
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
    • C12P13/00—Preparation of nitrogen-containing organic compounds
    • C12P13/002—Nitriles (-CN)
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
    • C12P13/00—Preparation of nitrogen-containing organic compounds
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
    • C12P13/00—Preparation of nitrogen-containing organic compounds
    • C12P13/001—Amines; Imines
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
    • C12P41/00—Processes using enzymes or microorganisms to separate optical isomers from a racemic mixture
    • C12P41/006—Processes using enzymes or microorganisms to separate optical isomers from a racemic mixture by reactions involving C-N bonds, e.g. nitriles, amides, hydantoins, carbamates, lactames, transamination reactions, or keto group formation from racemic mixtures
    • Y—GENERAL 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
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T436/00—Chemistry: analytical and immunological testing
    • Y10T436/20—Oxygen containing
    • Y10T436/200833—Carbonyl, ether, aldehyde or ketone containing
    • Y—GENERAL 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
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T436/00—Chemistry: analytical and immunological testing
    • Y10T436/20—Oxygen containing
    • Y10T436/207497—Molecular oxygen

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Zoology (AREA)
  • Wood Science & Technology (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Health & Medical Sciences (AREA)
  • General Chemical & Material Sciences (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • General Engineering & Computer Science (AREA)
  • Biotechnology (AREA)
  • Genetics & Genomics (AREA)
  • Biochemistry (AREA)
  • Microbiology (AREA)
  • Proteomics, Peptides & Aminoacids (AREA)
  • Analytical Chemistry (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Biomedical Technology (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Medicinal Chemistry (AREA)
  • Neurosurgery (AREA)
  • Animal Behavior & Ethology (AREA)
  • Neurology (AREA)
  • Preparation Of Compounds By Using Micro-Organisms (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
HK07110403.3A 2004-04-14 2007-09-25 Stereoselective bioconversion of aliphatic dinitriles into cyano carboxylic acids HK1105215A1 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US56213304P 2004-04-14 2004-04-14
PCT/IB2005/000873 WO2005100580A1 (en) 2004-04-14 2005-04-01 Stereoselective bioconversion of aliphatic dinitriles into cyano carboxylic acids

Publications (1)

Publication Number Publication Date
HK1105215A1 true HK1105215A1 (en) 2008-02-06

Family

ID=34962755

Family Applications (1)

Application Number Title Priority Date Filing Date
HK07110403.3A HK1105215A1 (en) 2004-04-14 2007-09-25 Stereoselective bioconversion of aliphatic dinitriles into cyano carboxylic acids

Country Status (44)

Country Link
US (2) US7727749B2 (xx)
EP (1) EP1745136B1 (xx)
JP (1) JP4051082B2 (xx)
KR (1) KR100887777B1 (xx)
CN (1) CN1942587B (xx)
AP (1) AP2301A (xx)
AR (1) AR048690A1 (xx)
AT (1) ATE445019T1 (xx)
AU (1) AU2005233371B2 (xx)
BR (1) BRPI0509908A (xx)
CA (1) CA2563307C (xx)
CR (2) CR8686A (xx)
CY (1) CY1109556T1 (xx)
DE (1) DE602005017027D1 (xx)
DK (1) DK1745136T3 (xx)
DO (1) DOP2005000055A (xx)
EA (1) EA010305B1 (xx)
EC (1) ECSP066917A (xx)
ES (1) ES2331140T3 (xx)
GE (1) GEP20084530B (xx)
GT (1) GT200500086A (xx)
HK (1) HK1105215A1 (xx)
HN (1) HN2005000162A (xx)
HR (1) HRP20090562T1 (xx)
IL (1) IL177918A (xx)
MA (1) MA28536B1 (xx)
ME (1) ME01107B (xx)
MY (1) MY144296A (xx)
NL (1) NL1028762C2 (xx)
NO (1) NO335624B1 (xx)
NZ (1) NZ549698A (xx)
PA (1) PA8629801A1 (xx)
PE (1) PE20060252A1 (xx)
PL (1) PL1745136T3 (xx)
PT (1) PT1745136E (xx)
RS (1) RS50994B (xx)
SI (1) SI1745136T1 (xx)
SV (1) SV2005002085A (xx)
TN (1) TNSN06329A1 (xx)
TW (1) TWI304095B (xx)
UA (1) UA82292C2 (xx)
UY (1) UY28851A1 (xx)
WO (1) WO2005100580A1 (xx)
ZA (1) ZA200607476B (xx)

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WO1998003167A1 (en) 1996-07-24 1998-01-29 Warner-Lambert Company Isobutylgaba and its derivatives for the treatment of pain
AT412092B (de) * 2003-02-27 2004-09-27 Dsm Fine Chem Austria Gmbh Verfahren zur herstellung chiraler alpha-hydroxycarbonsäuren durch enzymatische hydrolyse von chiralen cyanhydrinen
WO2006108151A1 (en) 2005-04-06 2006-10-12 Teva Pharmaceutical Industries Ltd. Crystalline forms of pregabalin
US7488846B2 (en) 2005-04-11 2009-02-10 Teva Pharmaceuical Industries Ltd. Pregabalin free of lactam and a process for preparation thereof
ATE523484T1 (de) 2005-05-10 2011-09-15 Teva Pharma Optische lösung a us 3-carbamoylmethyl-5-methyl- hexansäure
EP1879853A1 (en) 2005-05-10 2008-01-23 Teva Pharmaceutical Industries Ltd Pregabalin free of isobutylglutaric acid and a process for preparation thereof
ATE486841T1 (de) 2005-05-10 2010-11-15 Teva Pharma Verfahren zur herstellung von pregabalin und salzen daraus
CA2619472A1 (en) 2005-09-19 2007-03-29 Teva Pharmaceutical Industries Ltd. Chiral 3-carbamoylmethyl-5-methyl hexanoic acids, key intermediates for the new synthesis of (s)-pregabalin
US20070141684A1 (en) * 2005-12-21 2007-06-21 Pfizer Inc Preparation of gamma-amino acids having affinity for the alpha-2-delta protein
US7462738B2 (en) 2006-05-24 2008-12-09 Teva Pharmaceutical Industries Ltd. Processes for the preparation of R-(+)-3-(carbamoyl methyl)-5-methylhexanoic acid and salts thereof
WO2007143113A2 (en) * 2006-05-31 2007-12-13 Teva Pharmaceutical Industries Ltd. The use of enzymatic resolution for the preparation of intermediates of pregabalin
EP1881077A1 (en) * 2006-07-19 2008-01-23 Solvay Organics GmbH Process for the production of fluorine containing a-hydroxy carboxylic acids
BRPI0803092A2 (pt) 2007-03-22 2011-08-30 Teva Pharma sìntese de (s)-(+)-3-(aminometil)-5-metil ácido hexanóico, (s)-pregabalina
WO2009087650A2 (en) * 2007-10-15 2009-07-16 V.B. Medicare Pvt. Ltd. A novel process for synthesis of pregabalin from substituted cyclopropane intermediate and a process for enzymatic resolution of racemic pregabalin
US8546112B2 (en) 2008-05-21 2013-10-01 Sandoz Ag Process for the stereoselective enzymatic hydrolysis of 5-methyl-3-nitromethyl-hexanoic acid ester
US8614081B2 (en) 2009-07-23 2013-12-24 Codexis, Inc. Nitrilase biocatalysts
WO2011141923A2 (en) 2010-05-14 2011-11-17 Lupin Limited Improved synthesis of optically pure (s) - 3-cyano-5-methyl-hexanoic acid alkyl ester, an intermediate of (s)- pregabalin
US8604062B2 (en) * 2011-10-20 2013-12-10 Hoffman-La Roche Inc. Process for the preparation of isoxazolyl-methoxy nicotinic acids
US10023885B2 (en) 2012-11-07 2018-07-17 Hikal Limited Process for the preparation of pregabalin
WO2016075082A1 (en) 2014-11-10 2016-05-19 Sandoz Ag Stereoselective reductive amination of alpha-chiral aldehydes using omega-transaminases for the synthesis of precursors of pregabalin and brivaracetam
CN105017072B (zh) * 2015-06-30 2017-10-03 河北诚信有限责任公司 异丁基琥珀腈的合成方法
CN105176955B (zh) 2015-08-27 2018-11-02 浙江工业大学 来源于高山南芥的腈水解酶、基因、载体、工程菌及其应用
CN108424900B (zh) * 2018-02-09 2020-11-03 浙江工业大学 一种腈水解酶突变体及其构建方法和应用
CN114164197B (zh) * 2020-01-13 2023-08-18 浙江工业大学 一种热稳定性和活力提高的腈水解酶突变体及其应用
CN113651717A (zh) * 2021-08-05 2021-11-16 浙江工业大学 一种光学纯异丁基丁二腈的消旋方法

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Publication number Priority date Publication date Assignee Title
US5593871A (en) * 1990-09-20 1997-01-14 E. I. Du Pont De Nemours And Company Process for the preparation of enantiometric 2-alkanoic acid amides from nitriles
JP3218133B2 (ja) * 1993-02-03 2001-10-15 三菱レイヨン株式会社 フェニル基を有する光学活性α−ヒドロキシカルボン酸の製造法
US5637767A (en) 1995-06-07 1997-06-10 Warner-Lambert Company Method of making (S)-3-(aminomethyl)-5-methylhexanoic acid
US5858736A (en) 1996-05-17 1999-01-12 E. I. Du Pont De Nemours And Company Preparation of lactams from aliphatic α,ω-dinitriles
EP1032555B1 (en) 1997-10-27 2006-04-12 Warner-Lambert Company Llc Cyclic amino acids and derivatives thereof useful as pharmaceutical agents
US6642398B2 (en) 1999-06-10 2003-11-04 Warner-Lambert Company Mono-and disubstituted 3-propyl gamma-aminobutyric acids
US6551804B2 (en) 1999-07-12 2003-04-22 E. I. Du Pont De Nemours And Company Process for preparing 4-cyanopentanoic acid
US20040014195A1 (en) * 1999-12-29 2004-01-22 Diversa Corporation Nitrilases, nucleic acids encoding them and methods for making and using them
US6891059B2 (en) 2000-01-27 2005-05-10 Warner-Lambert Company Asymmetric synthesis of pregabalin
FR2824823A1 (fr) * 2001-05-21 2002-11-22 Aventis Animal Nutrition Sa Procede de preparation d'acides carboxyliques aliphatiques par hydrolyse enzymatique de composes nitriles aliphatiques
MXPA05013754A (es) * 2003-06-19 2006-03-08 Pfizer Prod Inc Una preparacion biocatalitica del acido 1-cianociclohexanoacetico.

Also Published As

Publication number Publication date
SV2005002085A (es) 2005-12-13
US8304252B2 (en) 2012-11-06
CA2563307C (en) 2011-02-08
PA8629801A1 (es) 2005-11-25
ECSP066917A (es) 2006-12-20
AP2006003764A0 (en) 2006-10-31
AU2005233371B2 (en) 2007-12-20
CN1942587A (zh) 2007-04-04
TNSN06329A1 (fr) 2008-02-22
ES2331140T3 (es) 2009-12-22
UY28851A1 (es) 2005-11-30
GT200500086A (es) 2006-01-10
TW200533756A (en) 2005-10-16
MY144296A (en) 2011-08-29
US20070196905A1 (en) 2007-08-23
IL177918A (en) 2013-11-28
JP2007532125A (ja) 2007-11-15
HN2005000162A (es) 2007-11-16
CR20110356A (es) 2011-07-21
CY1109556T1 (el) 2014-08-13
EP1745136B1 (en) 2009-10-07
NO335624B1 (no) 2015-01-12
US7727749B2 (en) 2010-06-01
JP4051082B2 (ja) 2008-02-20
NL1028762A1 (nl) 2005-10-17
ME01107B (me) 2012-12-20
EP1745136A1 (en) 2007-01-24
AR048690A1 (es) 2006-05-17
KR100887777B1 (ko) 2009-03-09
US20100204503A1 (en) 2010-08-12
GEP20084530B (en) 2008-11-10
EA010305B1 (ru) 2008-08-29
MA28536B1 (fr) 2007-04-03
TWI304095B (en) 2008-12-11
ZA200607476B (en) 2008-05-28
NL1028762C2 (nl) 2006-07-25
DE602005017027D1 (de) 2009-11-19
PL1745136T3 (pl) 2010-02-26
AU2005233371A1 (en) 2005-10-27
IL177918A0 (en) 2006-12-31
RS50994B (sr) 2010-10-31
CR8686A (es) 2006-11-21
PT1745136E (pt) 2009-11-26
NZ549698A (en) 2009-10-30
CA2563307A1 (en) 2005-10-27
HRP20090562T1 (en) 2009-11-30
NO20065181L (no) 2006-11-10
AP2301A (en) 2011-10-31
KR20070020009A (ko) 2007-02-16
ATE445019T1 (de) 2009-10-15
SI1745136T1 (sl) 2009-12-31
DOP2005000055A (es) 2005-12-15
EA200601574A1 (ru) 2007-04-27
CN1942587B (zh) 2010-05-05
WO2005100580A1 (en) 2005-10-27
UA82292C2 (uk) 2008-03-25
DK1745136T3 (da) 2009-11-30
PE20060252A1 (es) 2006-04-01
BRPI0509908A (pt) 2007-09-18

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Legal Events

Date Code Title Description
PC Patent ceased (i.e. patent has lapsed due to the failure to pay the renewal fee)

Effective date: 20180401