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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_ea1b68e771064dc02716ccad70b3f40a
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07F9-6561
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07F9-6561
filingDate 2020-02-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_dee00fa67408e88a1b42720afcf80543
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_3a0f9b71dbc445d8751e5581398d3069
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_3e2c6ebbc61462cf87a17b82c51fb6e7
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_28042fd7a580df96e1e6de0289c435e2
publicationDate 2021-08-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-113248538-A
titleOfInvention A kind of new synthetic method of remdesivir
abstract The invention discloses a new synthetic method for synthesizing Redcivir. The synthesis method of the present invention uses D-ribose as a raw material, and undergoes a series of reactions such as oxidation, cyclohexanone protection, silanization protection, substitution, substitution, deprotection, coupling, and deprotection to synthesize Redcivir. At the same time, the invention optimizes the post-processing operation, and has the advantages of short reaction time, high yield, low cost, and suitability for industrial production. The Remdesivir structure involved in the present invention is:
priorityDate 2020-02-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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