DE69620363D1 - Prozess für die produktion von optisch aktiven 1-halo-3-amino-4-phenyl-2-butanol derivaten - Google Patents

Prozess für die produktion von optisch aktiven 1-halo-3-amino-4-phenyl-2-butanol derivaten

Info

Publication number
DE69620363D1
DE69620363D1 DE69620363T DE69620363T DE69620363D1 DE 69620363 D1 DE69620363 D1 DE 69620363D1 DE 69620363 T DE69620363 T DE 69620363T DE 69620363 T DE69620363 T DE 69620363T DE 69620363 D1 DE69620363 D1 DE 69620363D1
Authority
DE
Germany
Prior art keywords
halo
phenyl
amino
optically active
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.)
Expired - Lifetime
Application number
DE69620363T
Other languages
English (en)
Other versions
DE69620363T2 (de
Inventor
Tadashi Sugawa
Kenji Inoue
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.)
Kaneka Corp
Original Assignee
Kaneka Corp
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 Kaneka Corp filed Critical Kaneka Corp
Publication of DE69620363D1 publication Critical patent/DE69620363D1/de
Application granted granted Critical
Publication of DE69620363T2 publication Critical patent/DE69620363T2/de
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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
    • C12P13/00—Preparation of nitrogen-containing organic compounds
    • C12P13/001—Amines; Imines
    • 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
    • Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S435/00—Chemistry: molecular biology and microbiology
    • Y10S435/8215—Microorganisms
    • Y10S435/822—Microorganisms using bacteria or actinomycetales
    • 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
    • Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S435/00—Chemistry: molecular biology and microbiology
    • Y10S435/8215—Microorganisms
    • Y10S435/911—Microorganisms using fungi

Landscapes

  • Organic Chemistry (AREA)
  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Zoology (AREA)
  • Engineering & Computer Science (AREA)
  • Wood Science & Technology (AREA)
  • Biotechnology (AREA)
  • Microbiology (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Proteomics, Peptides & Aminoacids (AREA)
  • Health & Medical Sciences (AREA)
  • Biochemistry (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • General Engineering & Computer Science (AREA)
  • General Health & Medical Sciences (AREA)
  • Genetics & Genomics (AREA)
  • Preparation Of Compounds By Using Micro-Organisms (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
DE69620363T 1995-06-19 1996-06-19 Prozess für die produktion von optisch aktiven 1-halo-3-amino-4-phenyl-2-butanol derivaten Expired - Lifetime DE69620363T2 (de)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP17682195A JP3529904B2 (ja) 1995-06-19 1995-06-19 光学活性１−ハロ−３−アミノ−４−フェニル−２−ブタノール誘導体の製造法
PCT/JP1996/001676 WO1997000327A1 (fr) 1995-06-19 1996-06-19 Procede pour produire des derives 1-halo-3-amino-4-phenyl-2-butanol optiquement actifs

Publications (2)

Publication Number Publication Date
DE69620363D1 true DE69620363D1 (de) 2002-05-08
DE69620363T2 DE69620363T2 (de) 2002-11-21

Family

ID=16020439

Family Applications (1)

Application Number Title Priority Date Filing Date
DE69620363T Expired - Lifetime DE69620363T2 (de) 1995-06-19 1996-06-19 Prozess für die produktion von optisch aktiven 1-halo-3-amino-4-phenyl-2-butanol derivaten

Country Status (7)

Country Link
US (1) US5726047A (de)
EP (1) EP0779366B1 (de)
JP (1) JP3529904B2 (de)
AT (1) ATE215607T1 (de)
DE (1) DE69620363T2 (de)
ES (1) ES2176463T3 (de)
WO (1) WO1997000327A1 (de)

Families Citing this family (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AU3075400A (en) * 1999-01-21 2000-08-07 Kaneka Corporation Method for purifying and isolating (2s,3s)- or (2r,3s)-halohydrin derivatives
US6835559B2 (en) 2000-03-28 2004-12-28 Daiichi Fine Chemical Co., Ltd. Process for the production of optically active β-amino alcohols
AU8069801A (en) 2000-08-16 2002-02-25 Bristol Myers Squibb Co Stereoselective reduction of substituted oxo-butanes
JP4792141B2 (ja) * 2005-01-19 2011-10-12 Ｈｏｙａ株式会社 モールドプレス成形型及び光学素子の製造方法
US7582468B2 (en) * 2005-05-25 2009-09-01 Bristol-Myers Squibb Company Process for preparing (2R,3S)-1,2-epoxy-3-(protected)amino-4-substituted butane and intermediates thereof
GB0619240D0 (en) * 2006-09-29 2006-11-08 Almac Sciences Ltd Reduction of alpha-halo ketones
PL2178513T3 (pl) * 2007-06-22 2011-09-30 Bristol Myers Squibb Holdings Ireland Kompozycje w tabletkach zawierające atazanawir
CN101801348A (zh) * 2007-06-22 2010-08-11 百时美施贵宝公司 含有阿扎那韦的压片组合物
AU2008268625B2 (en) * 2007-06-22 2013-11-28 Bristol-Myers Squibb Holdings Ireland Unlimited Company Tableted compositions containing atazanavir
EP2178512B1 (de) * 2007-06-22 2011-03-09 Bristol-Myers Squibb Company Tablettierte atazanavirhaltige zusammensetzungen
TWI601825B (zh) * 2007-09-27 2017-10-11 Ｉｅｐ有限公司 對映異構選擇性酶催化還原中間產物之方法

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4857468A (en) * 1985-04-13 1989-08-15 Kanegafuchi Kagaku Kogyo Kabushiki Kaisha Process for preparing optically active 2-halo-1-phenyl ethanol
CA1282549C (en) * 1985-11-12 1991-04-02 Eric M. Gordon Aminocarbonyl renin inhibitors
JPH0616714B2 (ja) * 1986-07-03 1994-03-09 鐘淵化学工業株式会社 光学活性（ｓ）−４−フエニル−２−ブタノ−ルの製造法
JPH0669B2 (ja) * 1986-07-03 1994-01-05 鐘淵化学工業株式会社 光学活性（ｒ）−４−フエニル−２−ブタノ−ルの製造法
CA1340588C (en) * 1988-06-13 1999-06-08 Balraj Krishan Handa Amino acid derivatives
DE69131685T2 (de) * 1990-07-24 2000-04-27 Kanegafuchi Chemical Ind Verfahren zur herstellung optisch aktiven (-)-2-halo-1-(substituiertes phenyl)ethanols

Also Published As

Publication number Publication date
US5726047A (en) 1998-03-10
ES2176463T3 (es) 2002-12-01
EP0779366B1 (de) 2002-04-03
DE69620363T2 (de) 2002-11-21
ATE215607T1 (de) 2002-04-15
JP3529904B2 (ja) 2004-05-24
JPH09285A (ja) 1997-01-07
EP0779366A4 (de) 1999-10-06
EP0779366A1 (de) 1997-06-18
WO1997000327A1 (fr) 1997-01-03

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