EA199901059A1 - Способ получения энантиомерно обогащенных n-производных лактамов - Google Patents

Способ получения энантиомерно обогащенных n-производных лактамов

Info

Publication number
EA199901059A1
EA199901059A1 EA199901059A EA199901059A EA199901059A1 EA 199901059 A1 EA199901059 A1 EA 199901059A1 EA 199901059 A EA199901059 A EA 199901059A EA 199901059 A EA199901059 A EA 199901059A EA 199901059 A1 EA199901059 A1 EA 199901059A1
Authority
EA
Eurasian Patent Office
Prior art keywords
enantiomerally
enriched
obtaining
lactams
derived
Prior art date
Application number
EA199901059A
Other languages
English (en)
Other versions
EA001964B1 (ru
Inventor
Майкл Джон Досон
Махмауд Махмаудиан
Кристофер Джон Уоллис
Original Assignee
Глаксо Груп Лимитед
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 Глаксо Груп Лимитед filed Critical Глаксо Груп Лимитед
Publication of EA199901059A1 publication Critical patent/EA199901059A1/ru
Publication of EA001964B1 publication Critical patent/EA001964B1/ru

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
    • 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
    • C12P13/02—Amides, e.g. chloramphenicol or polyamides; Imides or polyimides; Urethanes, i.e. compounds comprising N-C=O structural element or polyurethanes
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
    • C07D209/52—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring condensed with a ring other than six-membered
    • 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
    • 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)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Hydrogenated Pyridines (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Indole Compounds (AREA)

Abstract

Настоящее изобретение относится к способу получения по существу энантиомерно чистых промежуточных продуктов формулы (IV), где P представляет собой активирующую и защитную группу, из их рацематов путем обработки этой смеси ферментом ацилазой, получаемой из Bacillus sp.Международная заявка была опубликована вместе с отчетом о международном поиске.
EA199901059A 1997-08-22 1998-08-20 Способ получения энантиомерно обогащенных n-производных лактамов EA001964B1 (ru)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
GBGB9717928.7A GB9717928D0 (en) 1997-08-22 1997-08-22 Process for the enatioselective hydrolysis of n-derivatised lactams
PCT/EP1998/005291 WO1999010519A1 (en) 1997-08-22 1998-08-20 Process for preparing enantiomerically enriched n-derivatised lactams

Publications (2)

Publication Number Publication Date
EA199901059A1 true EA199901059A1 (ru) 2000-08-28
EA001964B1 EA001964B1 (ru) 2001-10-22

Family

ID=10817952

Family Applications (1)

Application Number Title Priority Date Filing Date
EA199901059A EA001964B1 (ru) 1997-08-22 1998-08-20 Способ получения энантиомерно обогащенных n-производных лактамов

Country Status (35)

Country Link
US (1) US6340587B1 (ru)
EP (1) EP1003903B1 (ru)
JP (1) JP3565868B2 (ru)
KR (1) KR100479894B1 (ru)
CN (1) CN1133749C (ru)
AP (1) AP1104A (ru)
AR (1) AR016395A1 (ru)
AT (1) ATE233323T1 (ru)
AU (1) AU738897B2 (ru)
BR (1) BR9810472B1 (ru)
CA (1) CA2295017A1 (ru)
CZ (1) CZ294302B6 (ru)
DE (1) DE69811677T2 (ru)
DK (1) DK1003903T3 (ru)
EA (1) EA001964B1 (ru)
EE (1) EE03934B1 (ru)
ES (1) ES2193568T3 (ru)
GB (1) GB9717928D0 (ru)
HK (1) HK1025796A1 (ru)
HR (1) HRP990408B1 (ru)
HU (1) HU222657B1 (ru)
ID (1) ID25830A (ru)
IL (1) IL133541A (ru)
IN (1) IN183908B (ru)
IS (1) IS2201B (ru)
NO (1) NO320081B1 (ru)
NZ (1) NZ501880A (ru)
PL (1) PL191108B1 (ru)
PT (1) PT1003903E (ru)
RS (1) RS49542B (ru)
SI (1) SI1003903T1 (ru)
SK (1) SK282782B6 (ru)
TR (1) TR199903210T2 (ru)
TW (1) TW589301B (ru)
WO (1) WO1999010519A1 (ru)

Families Citing this family (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DK1095160T3 (da) * 1998-07-09 2004-05-17 Lonza Ag Fremgangsmåde til fremstilling af (1R,4S)-2-azabicyclo[2.2.1]hept-5-en-3-on-derivater
DE19962543A1 (de) 1999-12-23 2001-07-05 Degussa Chromatographische Enantiomerentrennung von bicyclischen Lactamen
US6780635B2 (en) * 2001-12-27 2004-08-24 Council Of Scientific And Industrial Research Process for the preparation of optically active azabicyclo heptanone derivatives
EP1348765B1 (en) * 2002-03-28 2006-05-24 Council of Scientific and Industrial Research Process for the preparation of optically active azabicyclo heptanone derivatives
HU227663B1 (en) * 2007-07-09 2011-10-28 Univ Szegedi Resolution process
ES2969969T3 (es) 2010-01-27 2024-05-23 Viiv Healthcare Co Combinaciones de dolutegravir y lamivudina para el tratamiento de la infección por VIH
CN103695495B (zh) * 2014-01-14 2014-08-27 营口三征新科技化工有限公司 一种制备(1R,4s)-(-)-2-氮杂双环[2,2,1]庚-5-烯-3-酮的方法

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DK0424064T3 (da) * 1989-10-16 1995-06-26 Chiroscience Ltd Chirale azabicycloheptanoner og fremgangsmåde til fremstilling deraf
GB9108384D0 (en) 1991-04-19 1991-06-05 Enzymatix Ltd Bicycloheptanes
SK285228B6 (sk) * 1997-05-13 2006-09-07 Lonza Ag Spôsob výroby racemického alebo opticky aktívnehoderivátu 4-(hydroxymetyl)-2-cyklopenténu a racemicky N-butyryl-1-amino-4- (hydroxymetyl)-2-cyklopentén

Also Published As

Publication number Publication date
ID25830A (id) 2000-11-09
EE03934B1 (et) 2002-12-16
BR9810472A (pt) 2000-09-19
JP3565868B2 (ja) 2004-09-15
GB9717928D0 (en) 1997-10-29
IS5297A (is) 1999-12-14
PL191108B1 (pl) 2006-03-31
TR199903210T2 (xx) 2000-07-21
HUP0002661A2 (hu) 2000-12-28
WO1999010519A1 (en) 1999-03-04
ATE233323T1 (de) 2003-03-15
TW589301B (en) 2004-06-01
HRP990408A2 (en) 2000-04-30
SI1003903T1 (en) 2003-08-31
KR100479894B1 (ko) 2005-03-30
DE69811677T2 (de) 2003-10-16
KR20010014078A (ko) 2001-02-26
AU9738698A (en) 1999-03-16
NO996368D0 (no) 1999-12-21
NO320081B1 (no) 2005-10-17
SK282782B6 (sk) 2002-12-03
DK1003903T3 (da) 2003-06-10
AP9901721A0 (en) 1999-12-31
CA2295017A1 (en) 1999-03-04
NO996368L (no) 2000-02-21
YU69399A (sh) 2002-06-19
HU222657B1 (hu) 2003-09-29
AU738897B2 (en) 2001-09-27
IS2201B (is) 2007-02-15
HUP0002661A3 (en) 2001-12-28
BR9810472B1 (pt) 2011-01-11
CN1133749C (zh) 2004-01-07
HRP990408B1 (en) 2006-05-31
DE69811677D1 (de) 2003-04-03
RS49542B (sr) 2007-02-05
AP1104A (en) 2002-09-04
CN1261405A (zh) 2000-07-26
EP1003903A1 (en) 2000-05-31
HK1025796A1 (en) 2000-11-24
JP2001504354A (ja) 2001-04-03
US6340587B1 (en) 2002-01-22
PT1003903E (pt) 2003-06-30
IN183908B (ru) 2000-05-13
CZ471699A3 (cs) 2000-06-14
IL133541A0 (en) 2001-04-30
EP1003903B1 (en) 2003-02-26
PL337647A1 (en) 2000-08-28
SK184499A3 (en) 2000-09-12
AR016395A1 (es) 2001-07-04
NZ501880A (en) 2001-08-31
ES2193568T3 (es) 2003-11-01
EA001964B1 (ru) 2001-10-22
CZ294302B6 (cs) 2004-11-10
EE200000075A (et) 2000-10-16
IL133541A (en) 2003-10-31

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