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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D233-56
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D231-12
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D249-08
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D231-12
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D521-00
filingDate 1996-02-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_352c7a1377c300ecdc17d9ec92575464
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_85e1ad9def512701803f591a89a2dac2
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_cd25a2b69379b5d95d4be7b387de8c4e
publicationDate 1996-09-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber WO-9627589-A1
titleOfInvention Process for preparing n-substituted pyrazoles
abstract A process is disclosed for preparing N-substituted pyrazoles having the general formula (I), in which R<1> stands for C1 to C12 alkyl or C7 to C20 phenylalkyl, and R<2>, R<3>, R<4> represent independently from each other hydrogen, C1 to C12 alkyl, C7 to C20 phenylalkyl or optionally substituted aryl residues, by reacting pyrazoles having the general formula (II), in which R<2>, R<3> and R<4> have above-said meanings, with an alcohol having the general formula (III) R<1>-O-H, in which R<1> has above-said meanings, at temperatures from 50 to 400 DEG C in the presence of a catalyst. The reaction of pyrazole (II) with compound (III) is carried out in a molar ratio from 0.001:1 to 1:1 in the liquid phase at a slight negative pressure up to an overpressure of 250 bars. Acids, their alkyl esters and/or their anhydrides are used as catalysts in a molar ratio from 0.0001:1 to 0.5:1 in relation to pyrazole (II).
priorityDate 1995-03-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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