GB1469014A - Process for production of plus -2-amino-1-butanol - Google Patents

Process for production of plus -2-amino-1-butanol

Info

Publication number
GB1469014A
GB1469014A GB4244574A GB4244574A GB1469014A GB 1469014 A GB1469014 A GB 1469014A GB 4244574 A GB4244574 A GB 4244574A GB 4244574 A GB4244574 A GB 4244574A GB 1469014 A GB1469014 A GB 1469014A
Authority
GB
United Kingdom
Prior art keywords
aminobutyric acid
acyl
predominantly
amino
butanol
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
Application number
GB4244574A
Other languages
English (en)
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.)
Denka Co Ltd
Original Assignee
Denki Kagaku Kogyo KK
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 Denki Kagaku Kogyo KK filed Critical Denki Kagaku Kogyo KK
Publication of GB1469014A publication Critical patent/GB1469014A/en
Expired 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
    • 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
    • C12P41/007—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 by reactions involving acyl derivatives of racemic amines
    • 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

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Zoology (AREA)
  • Wood Science & Technology (AREA)
  • Health & Medical Sciences (AREA)
  • General Engineering & Computer Science (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Biotechnology (AREA)
  • Biochemistry (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Microbiology (AREA)
  • General Health & Medical Sciences (AREA)
  • Genetics & Genomics (AREA)
  • Analytical Chemistry (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Catalysts (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
  • Preparation Of Compounds By Using Micro-Organisms (AREA)
GB4244574A 1973-09-28 1974-09-30 Process for production of plus -2-amino-1-butanol Expired GB1469014A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP10897573A JPS5318006B2 (enExample) 1973-09-28 1973-09-28

Publications (1)

Publication Number Publication Date
GB1469014A true GB1469014A (en) 1977-03-30

Family

ID=14498384

Family Applications (1)

Application Number Title Priority Date Filing Date
GB4244574A Expired GB1469014A (en) 1973-09-28 1974-09-30 Process for production of plus -2-amino-1-butanol

Country Status (7)

Country Link
US (1) US3979457A (enExample)
JP (1) JPS5318006B2 (enExample)
DE (1) DE2446320C3 (enExample)
FR (1) FR2246519B1 (enExample)
GB (1) GB1469014A (enExample)
IT (1) IT1035089B (enExample)
NL (1) NL158169B (enExample)

Families Citing this family (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5547630A (en) * 1978-10-02 1980-04-04 Meiji Seika Kaisha Ltd Optical resolution of phosphorus-containing amino acid
US4205183A (en) * 1978-12-08 1980-05-27 Beckman Instruments, Inc. Facile method for isolating resolved amino acids
DE3334849A1 (de) * 1983-09-27 1985-04-04 Hoechst Ag, 6230 Frankfurt Verfahren zur racemisierung optisch aktiver aminosaeuren
DE3435095C2 (de) * 1984-09-25 1986-07-24 Degussa Ag, 6000 Frankfurt Verfahren zur Racemisierung von N-Acetyl-D(L)-α-aminocarbonsäuren
DE19505992C2 (de) * 1995-02-21 1997-04-10 Degussa Verfahren zur Herstellung von racemischen Aminoalkoholen
US7652039B2 (en) * 2002-05-17 2010-01-26 Sequella, Inc. Methods of use and compositions for the diagnosis and treatment of infectious disease
US7456222B2 (en) * 2002-05-17 2008-11-25 Sequella, Inc. Anti tubercular drug: compositions and methods
US20040033986A1 (en) * 2002-05-17 2004-02-19 Protopopova Marina Nikolaevna Anti tubercular drug: compositions and methods
EP1670314A4 (en) * 2003-09-05 2009-02-25 Sequella Inc METHODS AND COMPOSITIONS INCLUDE DIAMINE AS A NEW THERAPEUTIC FOR TUBERCULOSIS
US20090281054A1 (en) * 2008-05-06 2009-11-12 Venkata Reddy Compositions and methods comprising capuramycin analogues
EP4493708A1 (en) 2022-04-04 2025-01-22 University of the Witwatersrand, Johannesburg Enantioselective methods for preparing chiral amine intermediates
CN120944983A (zh) * 2025-08-05 2025-11-14 高唐奥瀚生物科技有限公司 一种固定化酶法制备l-2-氨基丁酸的工艺

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3116332A (en) * 1958-10-17 1963-12-31 Du Pont Resolution of racemic aminoisopropanol
US3553257A (en) * 1966-09-16 1971-01-05 American Cyanamid Co Preparation of d-2-amino-1-butanol salts
GB1198923A (en) * 1968-04-18 1970-07-15 Zoja Lab Chim Farm Process for the Preparation of the Dextrorotatory 2, 2', (Ethylenediimino)-di-1-butanoldihydrochloride
DE1768612A1 (de) * 1968-06-06 1971-11-18 Zoja Lab Chim Farm Verfahren zur Herstellung von sehr reinem,pharmazeutisch geeignetem rechtsdrehenden 2,2'-(AEthylendiimin)-di-1-butanoldihydrochlorid
US3769347A (en) * 1971-02-11 1973-10-30 American Cyanamid Co Production of d,d'-2,2'-(ethylenediimino) di-1-butanol hydrochloride

Also Published As

Publication number Publication date
IT1035089B (it) 1979-10-20
DE2446320C3 (de) 1978-09-07
DE2446320A1 (de) 1975-04-10
US3979457A (en) 1976-09-07
JPS5318006B2 (enExample) 1978-06-13
FR2246519B1 (enExample) 1976-10-22
JPS5069009A (enExample) 1975-06-09
NL158169B (nl) 1978-10-16
DE2446320B2 (de) 1978-01-05
FR2246519A1 (enExample) 1975-05-02
NL7412782A (nl) 1975-04-02

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Legal Events

Date Code Title Description
PS Patent sealed [section 19, patents act 1949]
PCNP Patent ceased through non-payment of renewal fee