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classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/Y02P20-52
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/B01J31-02
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C311-51
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filingDate 1996-08-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_dfd459946343d9fa70c270630cf0ee02
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e0819f6415afd126797733a168eb11cb
publicationDate 1998-02-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-H1045705-A
titleOfInvention Method for producing optically active acylsulfonamides
abstract (57) Abstract: A process for producing an acylsulfonamide derivative having an asymmetric carbon atom substituted with an oxy group at the α-position of a carbonyl group. SOLUTION: General formula (III) having an asymmetric carbon atom substituted by an oxy group at the α-position: To the optically active carboxylic acid represented by The reaction is carried out in an inert solvent at −30 ° C. to room temperature in an inert solvent to obtain a compound of the general formula (II): After the acid chloride represented by the general formula (I) V): embedded image Is reacted in an inert solvent in the presence of 2 to 8 equivalents of an inorganic base, or 1 to 2 equivalents of a compound represented by the formula (IV): Reacting .about.2 equivalents in an inert solvent in the absence of a base, characterized by the general formula (I): A process for producing acylsulfonamides having an optical purity of 95% or more, represented by the formula:
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