http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-102040547-B

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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C335-26
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G01N21-78
filingDate 2010-10-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2013-07-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a9fc19631830071b5c2cf57e372c7b2a
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1693a7f3a5d0b1d575ba9ae5ccebb36b
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4874f08d3ef9ba0db69b521d10f35839
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publicationDate 2013-07-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-102040547-B
titleOfInvention Salicyl thiourea derivative, preparation method and application
abstract The invention provides salicyl thiourea derivatives. The salicyl thiourea derivatives D1 and D2 are generated at high yield by reacting acetylsalicylic acid serving as a raw material and green solid phosgene serving as a chlorization reagent to obtain corresponding acyl chloride, reacting the acyl chloride with ammonium thiocyanate to obtain corresponding isothiocyanate under the catalysis of PEG-400, and performing an addition reaction on the isothiocyanate and arylamine. A preparation method has the advantages of simplicity and convenience in operation, mild reaction conditions, simplicity in aftertreatment and the like. A large number of studies discover that receptors D1 and D2 can identify F<->, Ac<-> and H2PO4<-> in DMSO (2*10<-3> to 3-2*10<-5> mol.L<-1>); and the D2 can realize specific selective identification in a system with 30 percent of H2O to 70 percent of DMSO.
priorityDate 2010-10-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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