http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CA-1214171-A
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_c7ad58d3c0b071069a8ee0cb8c8ba2e8 |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D253-075 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N43-707 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 |
| filingDate | 1982-08-27-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| grantDate | 1986-11-18-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_860b2e0250f96bdc759ec85b74a9ba5a |
| publicationDate | 1986-11-18-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | CA-1214171-A |
| titleOfInvention | Process for the preparation of 4-methyl-5-oxo-3- thioxo-tetrahydro-1,2,4-(2h, 4h)-triazines |
| abstract | A b s t r a c t Process for the preparation of 4-methyl-5-oxo-3-thioxo-tetrahydro-1,2,4-(2H, 4H)-triazines 4-methyl-5-oxo-3-thioxo-tetr2hydro-1,2,4-(2H,4H)-triazines,which are intermediate products for known herb-icides, can be prepared in high yields by a-process in which an acyl cyanide of the general formula R - C0 - 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 napthyl radical or an optionally substituted heterocyclic radical, is reacted with a carboxylic acid anhydride of the general formula R1 -CO-O-CO-R1 (III) 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 and 150°C, and the reaction mixture thus obtained is then reacted directly with 4-methyl-thiosemicarbazide (CH3-NH-CS-NH-NH2). |
| priorityDate | 1981-08-29-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 83.