http://rdf.ncbi.nlm.nih.gov/pubchem/patent/GB-1325280-A

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D215-42
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D471-04
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D215-42
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D471-04
filingDate 1972-03-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_73721ff34cc708be39123bfe4abca1ac
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_30f9265d640f53df222a1cb8d0a19479
publicationDate 1973-08-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber GB-1325280-A
titleOfInvention 3-substituted-as-triazino-5,6-c-quinolines
abstract 1325280 3 - Substituted - as - triazino[5,6-c]- quinolines MORTON-NORWICH PRODUCTS Inc 22 March 1972 [5 April 1971] 13497/72 Heading C2C Novel compounds of the Formula I wherein R is chloro, amino, 2-hydroxyethylamino, methoxy or diallylamino may be prepared by treating as-triazino[5,6-c]quinoline- 3(4-H)-one with phosphorus oxychloride to yield the compound I in which R is chloro and optionally reacting the product with ammonia, 2-aminoethanol, sodium methoxide or diallylamine respectively. The intermediate as-triazino[5,6-c]quinoline- 3(4H)-one may be prepared by reacting 4- chloro - 3 - nitroquinoline with ethyl carbazate to yield ethyl 3-(3-nitro-4-quinolyl)carbazate hydrochloride which is reduced to ethyl 3-(3- amino - 4 - quinolyl)carbazate hydrochloride which is cyclized with sodium methoxide to as - triazino[5,6-c]quinolin - 3 - ol sodium salt which on acidification yields the required ketone. Pharmaceutical compositions of the compounds I show antifungal activity when administered topically with the usual excipients.
priorityDate 1971-04-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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Total number of triples: 33.