http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-104945457-B

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07H1-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07H19-056
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P35-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07H19-056
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07H1-00
filingDate 2015-06-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2018-03-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 2018-03-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-104945457-B
titleOfInvention 1‑(1 ', 3 ', 4 ', 6 '-four O acetyl group α/β D glucopyanosyls)4 contraposition substituted aryl [1,2,3] triazoles and its preparation method and application
abstract With antitumor activity 1(1 ', 3 ', 4 ', 6 '-four O acetyl group α/β D glucopyanosyls)The preparation and its application of 4 contraposition substituted benzyl epoxide methyl [1,2,3] triazole series compounds, its core texture is substitution of 1,2,3 triazole derivatives on Isosorbide-5-Nitrae.Above-claimed cpd has good inhibitory activity to rectum cancer cell.It can be used as the medicine of the anti-carcinoma of the rectum.The synthetic method of above-claimed cpd includes:The preparation of the O acetyl group D glucose intermediates of 2 nitrine 1,3,4,6;The preparation of 4 contraposition substituted aryl base propargyl ethers;Click-reaction generation 1 occurs under monovalence copper catalysis in a solvent for the O acetyl group D glucose intermediate of 2 nitrine 1,3,4,6 and 4 contraposition substituted aryl propargyl ethers(1 ', 3 ', 4 ', 6 '-four O acetyl group α/β D glucopyanosyls)4 contraposition substituted benzyl epoxide methyl [1,2,3] triazole series compounds.
priorityDate 2015-06-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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