http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EA-200900628-A1
Outgoing Links
| Predicate | Object |
|---|---|
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K31-415 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P33-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D231-44 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N47-02 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N43-56 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P33-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N43-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N43-56 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-415 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D231-44 |
| filingDate | 2007-11-05-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationDate | 2009-12-30-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | EA-200900628-A1 |
| 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 acid and sulfonic derivatives isloty, adding a halogenating agent, wherein S represents [CFS (O)] O; or CFS (O) X, where X is fluoro, chloro, bromo, iodo, hydroxy or a salt of an alkali or alkaline earth metal of a hydroxy group; 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 |
Incoming Links
Total number of triples: 31.