http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-H045272-A

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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D211-90
filingDate 1990-04-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6481bf2453b6eb23ed454737494c038b
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d9f28f10a7a0cd54ccf81ac975130efe
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publicationDate 1992-01-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-H045272-A
titleOfInvention Preparation of 1,4-dihydropyridine derivative
abstract PURPOSE: To prepare nicardipine by reacting one of ester groups of 2,6- diomethyl-4-(3-nitrophenyl)-1,4-dihydropyridine-3,5-dicarboxylic acid dimethyl ester, with N-benzyl-N-methylaminoethanolate. n CONSTITUTION: A compound of formula I is reacted with a compound of formula II (M is a metal atom, particularly Na, K preferred), at 30-120°C for 2-70 hours to form a compound of formula III through the exchange of the ester. The compound of the formula II can be added as it is, but it can be effectively prepared in situ from N-benzyl-N-methylaminoethanol in the presence of a strong base such as Na, NaOH, KOCH 3 or the like. The reaction is performed in a solvent such as THF, toluene, dioxane or the like. The compound of the formula I is prepared by the reaction of 3-nitrobenzaldehyde, methyl acetoacetate, and ammonia. By the above-mentioned process, the compound of the formula III can be prepared with high purity and high yield. n COPYRIGHT: (C)1992,JPO
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-4951156-A
priorityDate 1990-04-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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