http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-103965059-B

Outgoing Links

Predicate Object
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C23-18
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C209-88
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C211-40
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C209-62
filingDate 2013-02-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2017-12-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 2017-12-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-103965059-B
titleOfInvention The method that one kind prepares (1R, 2S) 2 (3,4 difluorophenyl) cyclopropylamine
abstract The present invention relates to a kind of method of formula I (1R, 2S) 2 (3,4 difluorophenyl) cyclopropylamine;Described method is with 1 (3,4 difluorophenyls) ethene is raw material, successively Formulas I DL body is obtained by noval chemical compound formula IV, Formula V, split by the pure organic chiral acid of mapping, separation obtains Formulas I salt, free to obtain pure compound of formula I, Formulas I is preparation anticoagulant ticagrelor key intermediate;This method process safety, environment-friendly, cost is cheap, is adapted to large-scale production.
priorityDate 2013-02-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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