http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-107523594-B

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Predicate Object
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12P17-18
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D495-04
classificationIPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12R1-39
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D495-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12P17-18
filingDate 2017-03-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2018-08-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 2018-08-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-107523594-B
titleOfInvention The synthetic method of clopidogrel and its sulfate
abstract The invention discloses the synthetic methods of a kind of clopidogrel and its sulfate, include the following steps:O-chlorobenzaldehyde, nitrilation sodium, ammonium chloride reaction, 2 amino 2 (2 chlorphenyl) acetonitriles are generated, then generate 2 amino 2 (2 chlorphenyl) acetic acid under the effect of the catalyst, are split, purifying generates S 2 amino 2 (2 chlorphenyl) acetic acid;Methanol is added, reaction generates S 2 amino 2 (2 chlorphenyl) methyl acetate;It reacts, purifies in a solvent with α thiophene ethanol p-methyl benzenesulfonic acid esters, generate S α (2 thiophene ethylamino) 2 (2 chlorphenyl) methyl acetate;2 (2 chlorphenyl) methyl acetates of S α (2 thiophene ethylamino) are reacted with formaldehyde, and purifying obtains clopidogrel.Raw material supply of the present invention is sufficient, at low cost;Easily-controlled reaction conditions, easy to operate, technological process is simple, to equipment without particular/special requirement, is suitable for large-scale production.
priorityDate 2017-03-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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