http://rdf.ncbi.nlm.nih.gov/pubchem/patent/PL-397971-A1

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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-4196
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P25-08
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D249-12
filingDate 2012-02-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c9b0360edafd88e60f9019625b021db0
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publicationDate 2013-08-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber PL-397971-A1
titleOfInvention 5- (4-Chloro-phenyl) -4- (2,4-difluorophenyl) -2,4-dihydro-3H-1,2,4-triazol-3-thion derivative, method of its preparation and its first medical application
abstract A 1,2,4-triazole derivative of general formula 1 is described, which is 5- (4-chlorophenyl) -4- (2,4-difluorophenyl) -2,4-dihydro-3H-1,2,4-triazole Anticonvulsant 3-thionium and method of obtaining 5- (4-chlorophenyl) -4- (2,4-difluorophenyl) -2,4-dihydro-3H-1,2,4-triazole-3-thione of general formula 1 , in which the 4-chlorobenzoic acid hydrazide of formula II is reacted with 2,4-difluorophenyl isothiocyanate of formula 3, the reactions being carried out in a 1: 1 molar ratio, in polar solvents, at the boiling point of the solvent. The reaction mixture is cooled to room temperature and the resulting product 1 - [(4-chlorophenyl) carbonyl] -4- (2,4-difluorophenyl) thiosemicarbazide of formula 4 is filtered off, dried and crystallized from a suitable polar solvent, preferably from ethanol. It then cyclizes in an aqueous hydroxide solution at the boiling point of the solvent, and after cooling the solution is mixed with an aqueous acid solution.
priorityDate 2012-02-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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