http://rdf.ncbi.nlm.nih.gov/pubchem/patent/KR-20050108682-A

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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D211-90
filingDate 2004-05-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_11e0a3413653805f3d077260da4c965d
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_9641b0777ae25f3ac94416ace98ba823
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publicationDate 2005-11-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber KR-20050108682-A
titleOfInvention An improved synthetic method of lacidipine
abstract The present invention relates to an improved method for synthesizing lacidipine, and more particularly, to a method for synthesizing lacidipine, which has a simple process, easy reaction conditions, greatly improved yield, and mass production. In the present invention, phthalaldehyde and triphenylphosphoranylidene acetic acid 1,1-dimethylethyl ester are reacted to (E) -3- (2-formylphenyl) -2-propenic acid 1,1-dimethylethyl ester Preparing a first step; A second step of preparing lassidipine by reacting (E) -3- (2-formylphenyl) -2-propenic acid 1,1-dimethylethyl ester obtained in the above step with ethyl 3-aminocrotonate In the method of synthesizing lacidipine comprising the above step, the reaction is carried out at room temperature using tetrahydrofuran as a reaction solvent and recrystallized with hexane to obtain a yield of 100 ~ 110% (E) -3- (2 -Formylphenyl) -2-propenic acid 1,1-dimethylethyl ester crude product is obtained, and then the second step of the reaction is carried out as it is.
priorityDate 2004-05-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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