AU2009271325A1 - Biocatalytic processes for the preparation of substantially stereomerically pure fused bicyclic proline compounds - Google Patents

Biocatalytic processes for the preparation of substantially stereomerically pure fused bicyclic proline compounds Download PDF

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Publication number
AU2009271325A1
AU2009271325A1 AU2009271325A AU2009271325A AU2009271325A1 AU 2009271325 A1 AU2009271325 A1 AU 2009271325A1 AU 2009271325 A AU2009271325 A AU 2009271325A AU 2009271325 A AU2009271325 A AU 2009271325A AU 2009271325 A1 AU2009271325 A1 AU 2009271325A1
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AU
Australia
Prior art keywords
gly
ala
leu
ser
val
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.)
Abandoned
Application number
AU2009271325A
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English (en)
Inventor
Michael D. Clay
Jeffrey Colbeck
John M. Gruber
James Lalonde
Jack Liang
Jagadeesh Mavinhalli
Benjamin Mijts
Sheela Muley
John D. Munger Jr.
Lisa M. Newman
Roger Sheldon
Xiyun Zhang
Jun Zhu
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.)
Merck Sharp and Dohme LLC
Original Assignee
Merck Sharp and Dohme Ltd
Merck Sharp and Dohme LLC
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 Merck Sharp and Dohme Ltd, Merck Sharp and Dohme LLC filed Critical Merck Sharp and Dohme Ltd
Publication of AU2009271325A1 publication Critical patent/AU2009271325A1/en
Assigned to MERCK SHARP & DOHME CORP. reassignment MERCK SHARP & DOHME CORP. Request for Assignment Assignors: CODEXIS, INC.
Abandoned legal-status Critical Current

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Classifications

    • 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
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
    • C07D403/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
    • 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
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
    • C07D403/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
    • C07D487/04—Ortho-condensed systems
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D491/00—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
    • C07D491/02—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
    • C07D491/04—Ortho-condensed systems
    • 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
    • C12P13/24—Proline; Hydroxyproline; Histidine
    • 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
    • C12P17/10—Nitrogen as only ring hetero atom
    • 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
    • C12P17/18—Preparation of heterocyclic carbon compounds with only O, N, S, Se or Te as ring hetero atoms containing at least two hetero rings condensed among themselves or condensed with a common carbocyclic ring system, e.g. rifamycin
    • C12P17/188—Heterocyclic compound containing in the condensed system at least one hetero ring having nitrogen atoms and oxygen atoms as the only ring heteroatoms
    • 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
    • C12Y—ENZYMES
    • C12Y104/00—Oxidoreductases acting on the CH-NH2 group of donors (1.4)
    • C12Y104/03—Oxidoreductases acting on the CH-NH2 group of donors (1.4) with oxygen as acceptor (1.4.3)
    • C12Y104/03004—Monoamine oxidase (1.4.3.4)

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Wood Science & Technology (AREA)
  • Zoology (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Genetics & Genomics (AREA)
  • General Health & Medical Sciences (AREA)
  • General Engineering & Computer Science (AREA)
  • Health & Medical Sciences (AREA)
  • Biochemistry (AREA)
  • Microbiology (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Biotechnology (AREA)
  • Analytical Chemistry (AREA)
  • Preparation Of Compounds By Using Micro-Organisms (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Peptides Or Proteins (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Indole Compounds (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
AU2009271325A 2008-06-24 2009-06-23 Biocatalytic processes for the preparation of substantially stereomerically pure fused bicyclic proline compounds Abandoned AU2009271325A1 (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US7524308P 2008-06-24 2008-06-24
US61/075,243 2008-06-24
PCT/US2009/048255 WO2010008828A2 (en) 2008-06-24 2009-06-23 Biocatalytic processes for the preparation of substantially stereomerically pure fused bicyclic proline compounds

Publications (1)

Publication Number Publication Date
AU2009271325A1 true AU2009271325A1 (en) 2010-01-21

Family

ID=41550950

Family Applications (1)

Application Number Title Priority Date Filing Date
AU2009271325A Abandoned AU2009271325A1 (en) 2008-06-24 2009-06-23 Biocatalytic processes for the preparation of substantially stereomerically pure fused bicyclic proline compounds

Country Status (10)

Country Link
US (4) US8178333B2 (https=)
EP (2) EP2307419B1 (https=)
JP (1) JP2011525533A (https=)
KR (1) KR20110048509A (https=)
CN (2) CN102131813B (https=)
AU (1) AU2009271325A1 (https=)
CA (1) CA2728226A1 (https=)
ES (1) ES2438576T3 (https=)
MX (1) MX2010014500A (https=)
WO (1) WO2010008828A2 (https=)

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CN103450066B (zh) * 2012-05-30 2017-03-15 博瑞生物医药（苏州）股份有限公司 特拉匹韦中间体的制备方法
AR091192A1 (es) 2012-05-30 2015-01-21 Chemo Iberica Sa Procedimiento multicomponente para la preparacion de compuestos biciclicos
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CN105441401B (zh) * 2014-09-01 2019-11-08 上海弈柯莱生物医药科技有限公司 一种单胺氧化酶及其在合成手性氮杂双环化合物中的应用
CN105624128B (zh) * 2014-11-26 2020-03-17 上海弈柯莱生物医药科技有限公司 一种固定化单胺氧化酶及其在合成手性氮杂双环化合物中的应用
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CN114292825B (zh) * 2021-12-17 2023-08-18 武汉大学 一种托品酮的合成方法
CN114317631B (zh) * 2021-12-17 2023-11-07 武汉大学 单胺氧化酶在制备托品酮中的应用
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CN114774382A (zh) * 2022-04-07 2022-07-22 扬州联澳生物医药有限公司 立体选择性制备6,6-二甲基-3-氮杂双环[3.1.0]己烯化合物的方法
CN114751853B (zh) * 2022-04-11 2023-10-13 扬州联澳生物医药有限公司 6,6-二甲基-3-氮杂双环[3.1.0]己烷化合物的制备方法
CN114958938B (zh) * 2022-05-13 2023-12-08 金达威生物技术(江苏)有限公司 一种稠合二环脯氨酸甲酯盐酸盐的制备方法
CN114736882B (zh) * 2022-05-20 2023-09-22 苏州百福安酶技术有限公司 一种单胺氧化酶及其应用
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Also Published As

Publication number Publication date
US20100063300A1 (en) 2010-03-11
US8859784B2 (en) 2014-10-14
CN102131813A (zh) 2011-07-20
US20120244581A1 (en) 2012-09-27
ES2438576T3 (es) 2014-01-17
US20120289709A1 (en) 2012-11-15
KR20110048509A (ko) 2011-05-11
CA2728226A1 (en) 2010-01-21
EP2307419A4 (en) 2012-07-04
EP2307419A2 (en) 2011-04-13
US8178333B2 (en) 2012-05-15
EP2307419B1 (en) 2013-11-06
CN102816106A (zh) 2012-12-12
WO2010008828A2 (en) 2010-01-21
US8574876B2 (en) 2013-11-05
CN102131813B (zh) 2014-07-30
MX2010014500A (es) 2011-05-30
WO2010008828A3 (en) 2010-04-29
JP2011525533A (ja) 2011-09-22
EP2481737A1 (en) 2012-08-01
US20120130087A1 (en) 2012-05-24

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Owner name: MERCK SHARP & DOHME CORP.

Free format text: FORMER APPLICANT(S): CODEXIS, INC.

MK5 Application lapsed section 142(2)(e) - patent request and compl. specification not accepted