TW200502197A - Process for producing enantiopure β-amino acid derivatives, and enantiopureβ-amino acid derivatives - Google Patents

Process for producing enantiopure β-amino acid derivatives, and enantiopureβ-amino acid derivatives

Info

Publication number
TW200502197A
TW200502197A TW093109362A TW93109362A TW200502197A TW 200502197 A TW200502197 A TW 200502197A TW 093109362 A TW093109362 A TW 093109362A TW 93109362 A TW93109362 A TW 93109362A TW 200502197 A TW200502197 A TW 200502197A
Authority
TW
Taiwan
Prior art keywords
amino acid
acid derivatives
enantiopureβ
enantiopure
chr2
Prior art date
Application number
TW093109362A
Other languages
English (en)
Inventor
Roland Callens
Marc Larcheveque
Cyrille Pousset
Original Assignee
Solvay
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 Solvay filed Critical Solvay
Publication of TW200502197A publication Critical patent/TW200502197A/zh

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D207/04—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
    • C07D207/08—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon radicals, substituted by hetero atoms, attached to ring carbon atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D265/00—Heterocyclic compounds containing six-membered rings having one nitrogen atom and one oxygen atom as the only ring hetero atoms
    • C07D265/28—1,4-Oxazines; Hydrogenated 1,4-oxazines
    • C07D265/30—1,4-Oxazines; Hydrogenated 1,4-oxazines not condensed with other rings
    • 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
    • C12P13/04—Alpha- or beta- amino 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
    • C12P17/00—Preparation of heterocyclic carbon compounds with only O, N, S, Se or Te as ring hetero atoms
    • C12P17/14—Nitrogen or oxygen as hetero atom and at least one other diverse hetero ring atom in the same ring
    • 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
    • C12P41/003—Processes using enzymes or microorganisms to separate optical isomers from a racemic mixture by ester formation, lactone formation or the inverse reactions
    • C12P41/005—Processes 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
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
    • C07B2200/00—Indexing scheme relating to specific properties of organic compounds
    • C07B2200/07—Optical isomers
    • 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
    • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P20/00—Technologies relating to chemical industry
    • Y02P20/50—Improvements relating to the production of bulk chemicals
    • Y02P20/55—Design of synthesis routes, e.g. reducing the use of auxiliary or protecting groups

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Wood Science & Technology (AREA)
  • Zoology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Biotechnology (AREA)
  • Genetics & Genomics (AREA)
  • Microbiology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Biochemistry (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • General Engineering & Computer Science (AREA)
  • General Health & Medical Sciences (AREA)
  • Analytical Chemistry (AREA)
  • Preparation Of Compounds By Using Micro-Organisms (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
  • Pyrrole Compounds (AREA)
TW093109362A 2003-04-04 2004-04-05 Process for producing enantiopure β-amino acid derivatives, and enantiopureβ-amino acid derivatives TW200502197A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
FR0304219A FR2853327B1 (fr) 2003-04-04 2003-04-04 Procede pour la fabrication de derives de beta-aminoacides enantiopurs et derives de beta-aminoacides enantiopurs

Publications (1)

Publication Number Publication Date
TW200502197A true TW200502197A (en) 2005-01-16

Family

ID=32982246

Family Applications (1)

Application Number Title Priority Date Filing Date
TW093109362A TW200502197A (en) 2003-04-04 2004-04-05 Process for producing enantiopure β-amino acid derivatives, and enantiopureβ-amino acid derivatives

Country Status (11)

Country Link
US (1) US7592476B2 (zh)
EP (1) EP1613762B1 (zh)
JP (1) JP4712688B2 (zh)
CN (1) CN1768149B (zh)
AT (1) ATE485387T1 (zh)
AU (1) AU2004225796A1 (zh)
DE (1) DE602004029660D1 (zh)
DK (1) DK1613762T3 (zh)
FR (1) FR2853327B1 (zh)
TW (1) TW200502197A (zh)
WO (1) WO2004087940A2 (zh)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2876102A1 (fr) * 2004-10-04 2006-04-07 Solvay Compose heterocyclique enantiopur
HUP0600101A2 (en) * 2006-02-09 2007-09-28 Univ Szegedi Resolution process for the preparation of cyclic beta-amino acids esters there of
CN102956700B (zh) * 2011-08-30 2015-06-24 中国科学院微电子研究所 一种半导体结构及其制造方法

Family Cites Families (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3891616A (en) * 1974-04-17 1975-06-24 Squibb & Sons Inc Hypotensive {62 -homoaminoacid nonapeptides
DE69325698T2 (de) * 1992-12-21 2000-01-27 Duphar International Research B.V., Weesp Enzymatisches Verfahren zur stereoselektiven Herstellung einem Enantiomer aus einem hetero bicyclischen Alkohols
US5552318A (en) * 1995-05-26 1996-09-03 Industrial Technology Research Institute Method for preparing optically active amino acids and their esters using wheat germ lipase
PL334293A1 (en) * 1996-12-27 2000-02-14 Smithkline Beecham Plc Enzymatic separation of benzodiazepinacetic esters by means of lipase
CA2481839A1 (en) * 2002-04-08 2003-10-16 Ube Industries, Ltd. Process for producing either optically active n-substituted .beta.-amino acid and optically active n-substituted .beta.-amino acid ester or optically active n-substituted 2-homopipecolic acid and optically active n-substituted 2-homopipecolic acid ester
DE10220739A1 (de) * 2002-05-08 2003-11-27 Degussa Verfahren zur enzymatischen Herstellung enantiomerenangereicherter ß-Amionsäuren
US6869781B2 (en) * 2002-05-08 2005-03-22 Degussa Ag Process for the enzymatic preparation of enantiomer-enriched β-amino acids
DE10220740A1 (de) * 2002-05-08 2003-11-27 Degussa Verfahren zur enzymatischen Herstellung enantiomerenangereicherter beta-Aminosäuren

Also Published As

Publication number Publication date
FR2853327A1 (fr) 2004-10-08
CN1768149B (zh) 2012-10-31
CN1768149A (zh) 2006-05-03
DK1613762T3 (da) 2011-05-02
WO2004087940A3 (en) 2005-02-03
DE602004029660D1 (de) 2010-12-02
US7592476B2 (en) 2009-09-22
JP4712688B2 (ja) 2011-06-29
JP2006524043A (ja) 2006-10-26
ATE485387T1 (de) 2010-11-15
FR2853327B1 (fr) 2012-07-27
EP1613762A2 (en) 2006-01-11
WO2004087940A2 (en) 2004-10-14
US20060211097A1 (en) 2006-09-21
AU2004225796A1 (en) 2004-10-14
EP1613762B1 (en) 2010-10-20

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