http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-110684036-B

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classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/Y02P20-55
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C303-32
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D493-22
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D493-22
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C309-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C303-32
filingDate 2019-11-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2022-04-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 2022-04-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-110684036-B
titleOfInvention Method for preparing eribulin mesylate
abstract The invention relates to a preparation method of eribulin mesylate. The reaction involves reacting 2- [ (2S) -2-benzoyloxy ] -3- [ (2R,3R,3aS,7R,10S,11S,12S,13R,14S,15S,16E,21S,24S,27S,29R,31R,32aS) -12,13, 15-tris [ [ (1, 1-dimethylethyl) dimethylsilyl ] oxy ] -3,3a,4,5,6,7,8,9,10,11,12,13,14,15,18,19,20,21,22,23,24,25,26,27,28,29,30,31,32,32 a-triacontahydro-3-methoxy-29-methyl-23, 30-bis (methylene) -5, 18-dioxy-7, 11:10,14:21,24:27, 31-tetracyclooxy-2H-cyclotriundec [ b ] furan-2-yl ] propane The group ] -1H-phthalimide (N-ERBL-05) is used as an intermediate, and the eribulin mesylate is prepared through three steps of reactions.
priorityDate 2019-11-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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