http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-104725367-B

Outgoing Links

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D417-12
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D417-12
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P35-00
filingDate 2015-03-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2017-06-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 2017-06-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-104725367-B
titleOfInvention The ketoxime medicine of tetrahydro benzothiazol 7, preparation method and applications
abstract The present invention relates to the oxime compound of tetrahydro benzothiazol 7, the structural formula of the medicine includes the cis-isomer and transisomer of the ketoxime of tetrahydro benzothiazol 7: Medicine also includes above-mentioned cis-trans-isomer pharmaceutically acceptable salt (HX).Specific preparation process is that the cyclohexanedione (raw material 1) of 2 bromo 1,3 and thioamides flow back overnight under conditions of ethanol as solvent, obtains the ketone of 2 substituted-tetrahydro benzothiazole 7 (intermediate 2);Intermediate 2 and hydroxylamine hydrochloride are flowed back in anhydrous ethanol solvent under the effect of glacial acetic acid sodium, the ketoxime of 2 substituted-tetrahydro benzothiazole 7 (intermediate 3) is obtained;Intermediate 3 and propargyl bromide are dissolved in anhydrous acetonitrile, in the presence of sodium hydride, stirring reaction obtains the ketoxime ether of 2 substituted-tetrahydro benzothiazole 7 (intermediate 4);Intermediate 4 is made into catalyst in CuI and obtains the ketoxime class medicine of tetrahydro benzothiazol 7 with 1,3 Dipolar Cycloadditions of azide intermediate generation.And be applied in preparation treatment anti-gastric cancer medicament.
priorityDate 2015-03-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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