ES2176463T3 - Procedimiento para producir derivados de 1-halo-3-amino-4fenil-2-butanol opticamente activos. - Google Patents

Procedimiento para producir derivados de 1-halo-3-amino-4fenil-2-butanol opticamente activos.

Info

Publication number
ES2176463T3
ES2176463T3 ES96918833T ES96918833T ES2176463T3 ES 2176463 T3 ES2176463 T3 ES 2176463T3 ES 96918833 T ES96918833 T ES 96918833T ES 96918833 T ES96918833 T ES 96918833T ES 2176463 T3 ES2176463 T3 ES 2176463T3
Authority
ES
Spain
Prior art keywords
halo
amino
optically active
butanol
4fenil
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
ES96918833T
Other languages
English (en)
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
Application granted granted Critical
Publication of ES2176463T3 publication Critical patent/ES2176463T3/es
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)

Abstract

UN PROCEDIMIENTO PARA PRODUCIR DERIVADOS DE 1-HALO-3-AMINO-4FENILO-2-BUTANOL OPTICAMENTE ACTIVOS A PARTIR DE DERIVADOS DE 1HALO-3-AMINO-4-FENIL-2-BUTANONA OPTICAMENTE ACTIVOS ESTEREOSELECTIVAMENTE EN UN ALTO RENDIMIENTO MEDIANTE LA PUESTA EN CONTACTO DE LOS DERIVADOS DE BUTANONA CON MICROORGANISMOS.
ES96918833T 1995-06-19 1996-06-19 Procedimiento para producir derivados de 1-halo-3-amino-4fenil-2-butanol opticamente activos. Expired - Lifetime ES2176463T3 (es)

Applications Claiming Priority (1)

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

Publications (1)

Publication Number Publication Date
ES2176463T3 true ES2176463T3 (es) 2002-12-01

Family

ID=16020439

Family Applications (1)

Application Number Title Priority Date Filing Date
ES96918833T Expired - Lifetime ES2176463T3 (es) 1995-06-19 1996-06-19 Procedimiento para producir derivados de 1-halo-3-amino-4fenil-2-butanol opticamente activos.

Country Status (7)

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

Families Citing this family (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP4927258B2 (ja) * 1999-01-21 2012-05-09 株式会社カネカ （２ｓ，３ｓ）−又は（２ｒ，３ｓ）−ハロヒドリン誘導体の精製、単離方法
ES2284620T3 (es) 2000-03-28 2007-11-16 Daiichi Fine Chemical Co., Ltd. Proceso para la produccion de beta-amino alcoholes opticamente activos.
BR0113236B1 (pt) * 2000-08-16 2014-04-22 Bristol-Myers Squibb Company Processo estereosseletivo para a preparação de butanos(3S,2R)-1-halo-2-hidróxi-3-(protegido)amino-4-substituídos
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
DE602008005896D1 (de) * 2007-06-22 2011-05-12 Bristol Myers Squibb Co Tablettierte atazanavirhaltige zusammensetzungen
US20100178340A1 (en) * 2007-06-22 2010-07-15 Bristol-Myers Squibb Company Tableted compositions containing atazanavir
AU2008268627A1 (en) * 2007-06-22 2008-12-31 Bristol-Myers Squibb Company Tableted compositions containing atazanavir
SI2170292T1 (sl) * 2007-06-22 2014-05-30 Bristol-Myers Squibb Holdings Ireland Tabletirani sestavki, ki vsebujejo atazanavir
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 Kagaku Kogyo K.K., Osaka Verfahren zur herstellung optisch aktiven (-)-2-halo-1-(substituiertes phenyl)ethanols

Also Published As

Publication number Publication date
ATE215607T1 (de) 2002-04-15
JP3529904B2 (ja) 2004-05-24
DE69620363D1 (de) 2002-05-08
DE69620363T2 (de) 2002-11-21
EP0779366B1 (en) 2002-04-03
US5726047A (en) 1998-03-10
EP0779366A1 (en) 1997-06-18
JPH09285A (ja) 1997-01-07
EP0779366A4 (en) 1999-10-06
WO1997000327A1 (en) 1997-01-03

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