http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CA-1181067-A

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_c7ad58d3c0b071069a8ee0cb8c8ba2e8
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D251-38
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N43-64
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D251-38
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C313-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C337-08
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C67-00
filingDate 1982-02-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1985-01-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_618356260cd4fd586a05c07b217bb670
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e93c4b995511176045686e50ca090759
publicationDate 1985-01-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CA-1181067-A
titleOfInvention Process for the preparation of 1-amino-1,3,5-triazine- 2,4(1h, 3h)-diones
abstract ABSTRACT OF THE DISCLOSURE Herbicidal 1-amino-1,3,5-triazine-2,4(1H, 3H)-diones of the general formula (I) are obtained in good yields if an N-substituted O-aryl N-chlorocarbonyl carbamate of the general formula (II) is reacted with an isothiosemicarbazone of the general formula (III) or hydrohalide thereof, (R1 to R4 in formulae (I) to (III) having the meanings given in the description), at a temperature between 0 and 50°C, in the presence of an acid-binding agent, the open-chain intermediate products formed thereby are than heated (if appropriate without intermediate isolation), in a second stage, to a temperature between 50 and 150°C and, finally in a third stage, the 1-alkylldenosmlno-1,3,5 triazino-2,4(1H, 3H)-dione formed thereby is hydrolyzed if appropriate again without intermediate isolation) in an acid medium.
priorityDate 1981-02-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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