http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-102796105-B

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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D487-04
filingDate 2012-08-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2014-08-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_cf0d5b17df9219b28db0eea29944ad40
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_68739c75b22b429ac3c9c13fc6952eec
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d1c65df8e5e4340998ecf70862224845
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publicationDate 2014-08-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-102796105-B
titleOfInvention 2, 5, 6, 7-tetrahydropyrrolo[3, 4-c] pyridazine-3-one, its derivative and synthesis method thereof
abstract The invention relates to a medicinal intermediate 2, 5, 6, 7-tetrahydropyrrolo[3, 4-c] pyridazine-3-one with a structure shown in the following formula and its derivative, wherein R=H, -CO2Me, -CO2Et, -CO2Bu-T, -CO2CH2Ph or -CH2Ph. The preparation method comprises: taking N-R-pyrrolidin-3-one as a starting material, and reacting it with secondary amine to generate enamine; then subjecting ethyl glyoxylate and the enamine to a nucleophilic addition reaction, and reacting its product with hydrazine directly to form an aromatic ring, thus obtaining 6-R-2, 5, 6, 7-tetrahydropyrrolo[3, 4-c] pyridazine-3-one; and removing the substituent R, thus obtaining the 2, 5, 6, 7-tetrahydropyrrolo[3, 4-c] pyridazine-3-one. After further synthesis and modification, the compound can be transformed into molecules with the potential bioactivity of treating diseases of the cardiovascular system and the central nervous system.
priorityDate 2012-08-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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