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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D253-075
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D405-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D253-075
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D253-06
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N43-707
filingDate 1982-08-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1984-03-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_860b2e0250f96bdc759ec85b74a9ba5a
publicationDate 1984-03-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-4436905-A
titleOfInvention Preparation of 4-methyl-5-oxo-3-thioxo-tetrahydro-1,2,4,-(2H,4H)-triazines
abstract 4-Methyl-5-oxo-3-thioxo-tetrahydro-1,2,4-(2H,4H)-triazines, which are intermediate products for known herbicides, can be prepared in high yields by a process in which an acyl cyanide of the general formula R-CO-CN (II) wherein R represents an optionally substituted aliphatic radical having up to 12 carbon atoms, an optionally substituted cycloalkyl radical having 3 to 10 carbon atoms, an optionally substituted phenyl or naphthyl radical or an optionally substituted heterocyclic radical, is reacted with a carboxylic acid anhydride of the general formula R1-CO-O-CO-R1 (II) in which R1 represents an optionally substituted aliphatic radical having up to 8 carbon atoms or an optionally substituted phenyl radical, in the presence of a strong acid and, if appropriate, in the presence of a solvent, at a temperature between -50 DEG and 150 DEG C., and the reaction mixture thus obtained is then reacted directly with 4-methyl-thiosemicarbazide (CH3-NH-CS-NH-NH2).
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priorityDate 1981-08-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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