AU2002232037A1 - Synthesis of chiral intermediates useful in preparing pharmacologically active compounds - Google Patents

Synthesis of chiral intermediates useful in preparing pharmacologically active compounds

Info

Publication number
AU2002232037A1
AU2002232037A1 AU2002232037A AU3203702A AU2002232037A1 AU 2002232037 A1 AU2002232037 A1 AU 2002232037A1 AU 2002232037 A AU2002232037 A AU 2002232037A AU 3203702 A AU3203702 A AU 3203702A AU 2002232037 A1 AU2002232037 A1 AU 2002232037A1
Authority
AU
Australia
Prior art keywords
synthesis
active compounds
pharmacologically active
intermediates useful
chiral intermediates
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
AU2002232037A
Inventor
Raveendra Khandurao Tikare
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.)
Fermenta Biotech Ltd
Original Assignee
Fermenta Biotech Ltd
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 Fermenta Biotech Ltd filed Critical Fermenta Biotech Ltd
Publication of AU2002232037A1 publication Critical patent/AU2002232037A1/en
Abandoned legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D223/00Heterocyclic compounds containing seven-membered rings having one nitrogen atom as the only ring hetero atom
    • C07D223/14Heterocyclic compounds containing seven-membered rings having one nitrogen atom as the only ring hetero atom condensed with carbocyclic rings or ring systems
    • C07D223/16Benzazepines; Hydrogenated benzazepines
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C255/00Carboxylic acid nitriles
    • C07C255/01Carboxylic acid nitriles having cyano groups bound to acyclic carbon atoms
    • C07C255/32Carboxylic acid nitriles having cyano groups bound to acyclic carbon atoms having cyano groups bound to acyclic carbon atoms of a carbon skeleton containing at least one six-membered aromatic ring
    • C07C255/36Carboxylic acid nitriles having cyano groups bound to acyclic carbon atoms having cyano groups bound to acyclic carbon atoms of a carbon skeleton containing at least one six-membered aromatic ring the carbon skeleton being further substituted by hydroxy groups
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D207/00Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D207/02Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D207/04Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
    • C07D207/10Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D207/16Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D209/00Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D209/02Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D209/00Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D209/02Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
    • C07D209/04Indoles; Hydrogenated indoles
    • C07D209/30Indoles; Hydrogenated indoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to carbon atoms of the hetero ring
    • C07D209/42Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D233/00Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
    • C07D233/04Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
    • C07D233/28Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D233/30Oxygen or sulfur atoms
    • C07D233/32One oxygen atom
    • C07D233/38One oxygen atom with acyl radicals or hetero atoms directly attached to ring nitrogen atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D487/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02Heterocyclic 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
    • C07D487/04Ortho-condensed systems
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D495/00Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
    • C07D495/02Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
    • C07D495/10Spiro-condensed systems
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12NMICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N9/00Enzymes; Proenzymes; Compositions thereof; Processes for preparing, activating, inhibiting, separating or purifying enzymes
    • C12N9/88Lyases (4.)
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12PFERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
    • C12P13/00Preparation of nitrogen-containing organic compounds
    • C12P13/002Nitriles (-CN)
    • C12P13/004Cyanohydrins
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12PFERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
    • C12P13/00Preparation of nitrogen-containing organic compounds
    • C12P13/04Alpha- or beta- amino acids
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07BGENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
    • C07B2200/00Indexing scheme relating to specific properties of organic compounds
    • C07B2200/07Optical isomers
    • YGENERAL 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
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02PCLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P20/00Technologies relating to chemical industry
    • Y02P20/50Improvements relating to the production of bulk chemicals
    • Y02P20/582Recycling of unreacted starting or intermediate materials

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Zoology (AREA)
  • Engineering & Computer Science (AREA)
  • Wood Science & Technology (AREA)
  • Health & Medical Sciences (AREA)
  • Genetics & Genomics (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • General Engineering & Computer Science (AREA)
  • General Health & Medical Sciences (AREA)
  • Microbiology (AREA)
  • Biotechnology (AREA)
  • Biochemistry (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Molecular Biology (AREA)
  • Medicinal Chemistry (AREA)
  • Biomedical Technology (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Preparation Of Compounds By Using Micro-Organisms (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Peptides Or Proteins (AREA)
AU2002232037A 2000-11-23 2001-11-21 Synthesis of chiral intermediates useful in preparing pharmacologically active compounds Abandoned AU2002232037A1 (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
GB0028523A GB2369615B (en) 2000-11-23 2000-11-23 Process
GB0028523.9 2000-11-23
PCT/IB2001/002794 WO2002042244A2 (en) 2000-11-23 2001-11-21 Synthesis of chiral intermediates useful in preparing pharmacologically active compounds

Publications (1)

Publication Number Publication Date
AU2002232037A1 true AU2002232037A1 (en) 2002-06-03

Family

ID=9903694

Family Applications (1)

Application Number Title Priority Date Filing Date
AU2002232037A Abandoned AU2002232037A1 (en) 2000-11-23 2001-11-21 Synthesis of chiral intermediates useful in preparing pharmacologically active compounds

Country Status (8)

Country Link
US (1) US20040048346A1 (en)
EP (1) EP1335988A2 (en)
JP (1) JP2004514662A (en)
AU (1) AU2002232037A1 (en)
BR (1) BR0115570A (en)
CA (1) CA2427473A1 (en)
GB (1) GB2369615B (en)
WO (1) WO2002042244A2 (en)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8547440B2 (en) * 2010-01-29 2013-10-01 Nokia Corporation Image correction for image capturing with an optical image stabilizer
WO2011099029A1 (en) * 2010-02-15 2011-08-18 Laila Nutraceuticals A novel boswellia low polar gum resin extract and its synergistic compositions
CN111733192B (en) * 2020-07-03 2021-12-03 湖北大学 Novel enzyme catalysis method for preparing cinnamic acid from cinnamaldehyde and application
EP4001422A1 (en) 2020-11-20 2022-05-25 Enzymaster Deutschland GmbH Preparation of optically active cyanohydrins from aldehydes and ketones using a biphasic hydroxynitrile lyase-catalyzed hydrocyanation process

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH02229135A (en) * 1989-02-28 1990-09-11 Kyowa Gas Chem Ind Co Ltd Production of 2-hydroxy-4-phenylbutyric acid
EP0547655A1 (en) * 1991-12-11 1993-06-23 Duphar International Research B.V Method of preparing optically active cyanohydrins
US5552317A (en) * 1995-05-26 1996-09-03 Industrial Technology Research Institute Method for preparing optically active homophenylalanine and esters thereof using lipase from wheat germ or Candida lipolytica

Also Published As

Publication number Publication date
GB2369615A (en) 2002-06-05
GB2369615B (en) 2002-12-11
US20040048346A1 (en) 2004-03-11
JP2004514662A (en) 2004-05-20
EP1335988A2 (en) 2003-08-20
WO2002042244A3 (en) 2002-08-15
BR0115570A (en) 2004-02-25
GB2369615A8 (en) 1900-01-01
GB0028523D0 (en) 2001-01-10
CA2427473A1 (en) 2002-05-02
WO2002042244A2 (en) 2002-05-30

Similar Documents

Publication Publication Date Title
AU3771100A (en) Synthesis of epothilones
IL214165A0 (en) Intermediates useful in the synthesis of statin derivatives
AU2002213248A1 (en) Synthesis of epothilones and relates analogs
AU3565999A (en) Synthesis of azetidine derivatives
HK1084114A1 (en) Compounds for synthesizing intermediate useful in the preparation of atorvastatin
AU7830400A (en) Synthesis of insulin derivatives
AU2003245572A1 (en) Preparation of chiral amino-nitriles
AU2001269063A1 (en) Shortened synthesis of 3,3-diarylpropylamine derivatives
AU2001244692A1 (en) Novel crystal form of pyrrolidylthiocarbapenem derivative
AU2001285325A1 (en) Use of threo-methylphenidate compounds to enhance memory
AU2001269685A1 (en) Crystallization of 4-diphosphocytidyl-2-c-methylerythritol synthesis
AU2001268589A1 (en) Cross linked solid supports for solid phase synthesis
AU2002232037A1 (en) Synthesis of chiral intermediates useful in preparing pharmacologically active compounds
AU5587200A (en) Synthesis of substituted amidines
AU2002316593A1 (en) Solid phase synthesis of arylretinamides
AU2252101A (en) New synthesis of SPLA2 inhibitors
AU7918200A (en) Oxidation process for the preparation of intermediates useful in the synthesis of diarylpyridines
AU2001277728A1 (en) Biphenylcarboxamidoisoindoline compounds, processes for the preparation of the same and intermediates for the synthesis thereof
AU2002358357A1 (en) Improvements relating to frequency synthesis
GB0112322D0 (en) Synthesis of chiral intermediates
AU2001232752A1 (en) Intermediates for biologically active compounds
AU2001277801A1 (en) Process for preparing 2,3-diaminopropanols and synthesis of other compounds using 2,3-diaminopropanols
AU1695901A (en) Process for the preparation of intermediates useful in the synthesis of diarylpyridines
AU2001243435A1 (en) Intermediates useful for the synthesis of huperzine a
AU3790200A (en) Synthesis of intermediates useful in preparing tricyclic compounds