http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EA-016304-B1

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filingDate 2007-11-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_9c2adced89f8d75b368ffcae1aeabb11
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a720a8eaa4b29726c2d6e6bf31271774
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_0e28a214189463466f8c96116ff143f4
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_25b79a95ba54f63641657e0243802ffd
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1b5709cd7724590d211a61ddee04eb50
publicationDate 2012-04-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EA-016304-B1
titleOfInvention METHOD OF SULPHINYLATION OF DERIVATIVE PYRAZOL
abstract The present invention relates to a new method for sulfinylation of a pyrazole derivative, characterized in that 5-amino-1- [2,6-dichloro-4- (trifluoromethyl) phenyl] -1H-pyrazole-3-carbonitrile (II) is reacted with a sulfinylating agent S in the presence of at least one amino / acid complex in which the amine (s) is (are) selected from secondary and / or tertiary amines and the acid (s) is (are) selected from fluoride hydrochloric, hydrochloric, hydrobromic and hydroiodic acids and derivatives of sulfones acid minutes, adding a halogenating agent, wherein S represents [CFS (O)] O or CFS (O) X, wherein X is fluoro, chloro, bromo, iodo, hydroxy, or a salt of an alkali or alkaline earth metal hydroxy; or mixtures thereof, where the temperature of the reaction mixture never exceeds 39 ° C.
priorityDate 2006-11-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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Total number of triples: 409.