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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D265-32
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D413-14
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D209-48
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D413-14
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D265-32
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D209-48
filingDate 2014-04-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2017-12-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 2017-12-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-105085508-B
titleOfInvention A kind of method for synthesizing razaxaban key intermediate
abstract The invention discloses one kind to synthesize razaxaban key intermediate (S) 2 { [base of 2 oxygen 3 (4 (3 oxygen morpholine) phenyl) oxazolidine 5] methyl } iso-indoles 1, the method of 3 diketone, 4 (4 first ammonia alkenyl phenyl) 3 morpholones and (S) { 1 (chloro-carbonic acid ester group) 2 [2 (1,3 dioxy iso-indoles) base] ethyl } halide salt are carried out into ring closure reaction to produce.This method is easy to operate, raw material is easy to get, yield may be up to 90% or so, obtained (S) 2 { [base of 2 oxygen 3 (4 (3 oxygen morpholine) phenyl) oxazolidine 5] methyl } iso-indoles 1,3 diketone purity are good, purity may be up to more than 98%, be suitably applied industrialized production.
priorityDate 2014-04-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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