http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2018113710-A1

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classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/Y02P20-55
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07H19-12
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07H19-12
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filingDate 2017-12-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_706e954022e16d611cb3c7db311c3cb9
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6f903ff5f6cf385ffd8b209c97cf630a
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publicationDate 2018-06-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber WO-2018113710-A1
titleOfInvention METHOD FOR PREPARING β-NUCLEOSIDE COMPOUND
abstract Provided in the present invention is a method for preparing a β -nucleoside compound, comprising the steps of: 1) performing a silylation reaction of a nitrogenous base or an analogue thereof in the presence of TMSOTf to obtain the nitrogenous base or the analogue thereof being protected by trimethylsilyl; 2) performing a direct glycosylation reaction of the reaction liquid, without being isolated, and a five- or six-membered ring saccharide or a derivative thereof closed by a hydroxy protecting group to obtain a closed β -nucleoside compound; and 3) performing a deprotection reaction to obtain the β -nucleoside compound. The method uses a one-pot process to prepare the key intermediate of the β -nucleoside compound, and the yield of the β -configuration substance increases significantly. The method has the advantages of a simple operation, saving energy and protecting the environment, and is suitable for industrial application.
priorityDate 2016-12-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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