http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-113004352-B

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Predicate Object
classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/Y02P20-55
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07H15-18
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07H1-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07H15-04
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07H15-18
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07H15-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07H1-00
filingDate 2018-11-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2022-04-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 2022-04-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-113004352-B
titleOfInvention Preparation method of fondaparinux sodium and fondaparinux sodium monosaccharide intermediate
abstract The invention discloses a fondaparinux sodium and a preparation method of a fondaparinux sodium monosaccharide intermediate, which takes glucosamine protected at C4 and C6 as raw materials, obtaining methyl 3-O-benzyl-4, 6-O-benzylidene-2- (benzyloxycarbonyl) amino-2-deoxy-alpha-D-glucopyranoside through methylation, amidation and benzylation, then, a dehydroxylation protecting group protection reaction is carried out to obtain a fondaparinux sodium monosaccharide fragment intermediate methyl3-O-benzyl-2- (benzyloxycarbonyl) amino-2-deoxy-alpha-D-glucopyranoside, and the fondaparinux sodium is prepared from the intermediate methyl3-O-benzyl-2- (benzyloxycarbonyl) amino-2-deoxy-alpha-D-glucopyranoside. The preparation method has the advantages of simple process, less side reaction impurities and high yield, and is suitable for large-scale preparation of fondaparinux sodium in order to meet the requirement of industrial production of fondaparinux sodium.
priorityDate 2018-11-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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