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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12P41-00
filingDate 1992-09-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_bb320b6157f6e51277096fb8e5fd23da
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publicationDate 1994-04-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-H0690790-A
titleOfInvention Process for producing optically active 1,4-dihydropyridine-3,5-dicarboxylic acid / monoester derivative
abstract (57) [Summary] [Structure] The compound represented by the formula (I) is asymmetrically hydrolyzed by the action of a protease, and the obtained optically active 1,4-dihydropyridine compound represented by the formula (II) is collected. Optically active (4R) -1,4-dihydro-characterized in that 2,6-Dimethyl-4- (nitrophenyl) pyridine- Method for producing 3,5-dicarboxylic acid / monoester derivative (wherein R represents a CN group, NO 2 group, R 1 S (O) n group, or COOH group; R 1 is a lower alkyl, substituted Represents an optionally substituted aryl group or an optionally substituted aralkyl group, and n is an integer of 0 to 2). [Chemical 1] [Effect] The compound of formula (II) useful as a pharmaceutical intermediate can be easily obtained with high optical purity.
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