http://rdf.ncbi.nlm.nih.gov/pubchem/patent/GB-1212273-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
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N43-707
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D253-075
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N43-707
filingDate 1968-07-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_60541e50dc6982396d5afad38175d167
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_80098fd6ba37f100275f8402efa7a9ca
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c20eee404e1ec361569aa815998d28fd
publicationDate 1970-11-11-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber GB-1212273-A
titleOfInvention 0,2,4-triazine-5-ones
abstract 1,212,273. Triazinone derivatives. FARBENFABRIKEN BAYER A.G. 24 July, 1968 [18 Aug., 1967; 22 March, 1968], No. 35333/68. Heading C2C. [Also in Division A5] Novel 1,2,4-triazine-5-ones of the formula in which R is an aliphatic hydrocarbon, cycloaliphatic hydrocarbon, araliphatic hydrocarbon, alkoxycarbonyl, heterocyclic or aryl radical, these radicals possibly being substituted by halogen, nitro, alkyl, alkoxy, alkylmercapto, alkoxycarbonyl and/or carbonyl, R<SP>1</SP> is a hydrogen or an aliphatic hydrocarbon or aryl radical, these radicals possibly being substituted by the substituents named in the definition of R, Y is R<SP>11</SP> is an alkyl, alkenyl or aralkyl radical, these radicals possibly being substituted by halogen and/or nitro, R<SP>111</SP> is hydrogen or an alkyl radical, or R<SP>11</SP> and R<SP>111 </SP>together with the nitrogen atom are a heterocyclic radical are prepared by (a) reacting a compound of tautomeric formula with R<SP>11</SP>-Hal to give compounds in which Y is -SR<SP>11</SP>; (b) reacting compounds in which Y is -SR<SP>11</SP> with R<SP>11</SP>OM (M=alkali metal) or HNR<SP>11</SP>R<SP>111</SP> to convert Y to -OR<SP>11</SP> or - NR<SP>11</SP>R<SP>111</SP>, (c) reacting benzoylformic acid ethyl ester with N-methyl-N<SP>1</SP>-methyl-aminoguanidine hydroiodide to give the product in which R = C 6 H 5 -, R<SP>1</SP>= , R<SP>11</SP> = CH 3 , R<SP>111</SP> = H. Numerous compounds of the above tautomeric formula are prepared by reacting RCOCOOH with H 2 NNHCSNHR<SP>1</SP>.
priorityDate 1967-08-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

Incoming Links

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Total number of triples: 31.