http://rdf.ncbi.nlm.nih.gov/pubchem/patent/SU-1456434-A1

Outgoing Links

Predicate Object
assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_c4c2a511a2086c8ccc1c65796c28d672
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D487-04
filingDate 1987-01-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1989-02-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e220fdf4e2295c6b7ff8510f8f88fcee
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6122fbb7ae0a8d07fa479321d9a8b532
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_0cfab6b13ef323f9004c392dfa3ec1a3
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e0609b54feb003f3b76d6399efbf32f8
publicationDate 1989-02-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber SU-1456434-A1
titleOfInvention 9-methoxy-4-phenyl-1(4n)-oxopyridazino/3,4-c/cynnolines
abstract The invention relates to a heterocyclic compound, in particular 9-methoxy-4-phenyl-1 (4H) -oxopyridazino C3,4-c cinnolines, containing in position 2 methyl or cyano group and in position 8 methoxy group or hydrogen, which can be used as active substances or as intermediates for their synthesis. The goal is to create new structural bonds for heterocyclic substances. Their synthesis is carried out by the reaction of 6-amino-5-aryl-1-phenyl-1H-pyridazinone-4 with sodium nitrite in acetic acid at room temperature for 15-30 hours. Yield,%; t.p. &amp;C; Gross f-a: a) 80, 280, C, gH (N + OI; b) 78, 227, c) 85,6,290, C, 9H, K40e. 3 il. te
priorityDate 1987-01-12-04:00^^<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: 24.