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http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_1195105daef381efe9b92af8e8a56a63
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P3-10
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07H17-02
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P3-10
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07H17-02
filingDate 2019-01-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2022-07-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b022c0137c0238e9e8df2270ce00a9db
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_0f2aea01309b9b97a63616b3df361bbe
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b8e4cba53d4728d561990b69da190d47
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d4cccd0989a7f004a14c9a6fb0e51f1c
publicationDate 2022-07-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-11377465-B2
titleOfInvention Pyranoglucose-substituted pyrazole compound, preparation method thereof and application thereof
abstract A pyranoglucose-substituted pyrazole compound, used as a pharmaceutical intermediate, having the structural formula represented by formula (9c). The present invention further relates to an intermediate compound represented by formula (10c) or a salt thereof. The present invention further relates to a preparation method of the aforementioned intermediate compound and a method of using the same to prepare an SGLT inhibitor. By means of the novel key intermediate, the preparation technique of an SGLT inhibitor is greatly simplified. In addition, because the intermediate can be precipitated in the form of a salt and is easy to purify, the purity of the SGLT inhibitor is significantly increased, compared with the original preparation pathway (crude product purity can reach 99% or more). (I)
priorityDate 2018-01-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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