http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-S6110588-A

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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D311-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P37-08
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-435
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D221-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D491-052
filingDate 1985-01-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b7ef2dfcf2a6b4130683d11ecbb21ab1
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_14b4535ff4cd736bb445a2d85f953919
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publicationDate 1986-01-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-S6110588-A
titleOfInvention 1-azaxanthone derivative and preparation thereof
abstract NEW MATERIAL:A compound expressed by formula I [ring A is substituted by halogen, nitro, alkyl, alkoxyl or butadienylene group (-CH=CH-CH=CH-) forming benzene ring with the two adjacent carbon atoms at the 6-, 7-, 8- and 9-positions; R1 is H, alkyl, phenyl, amino, alkoxycarbonyl or OH; R2 is cyano, alkoxycarbonyl or -CONH2]. EXAMPLE:Ethyl 7-ethyl-2-methyl-1-azaxanthone-3-carboxylate. USE:An antiallergic agent. PREPARATION:A compound expressed by formula II, e.g. 2-amino-6-ethyl-4-oxo- 4H-1-benzopyran-3-carboxaldehyde, is reacted with an active methylene compound, e.g. ethyl acetoacetate, or an acetylenecarboxylic acid derivative.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-5952338-A
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priorityDate 1985-01-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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