http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-H07224058-A

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_01249be6ad92a1f01c99b5987ca16162
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-55
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P37-08
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D403-04
filingDate 1994-02-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_fbe43855b942a475bedf494719099a32
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_999651c94e031e10a7c3cda55c853768
publicationDate 1995-08-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-H07224058-A
titleOfInvention Process for producing 4- (p-chlorobenzyl) -2- (hexahydro-1-methyl-1H-azepin-4-yl) -1 (2H) -phthalazinone or a salt thereof
abstract (57) [Summary] [Structure] 4- (p-chloro-1-cyanobenzyl)- 4- (p-chloro-1-cyanobenzyl) -2-by reacting 1 (2H) -phthalazinone with 1-methyl-1-azoniabicyclo [3.2.0] -heptane chloride. (Hexahydro-1-methyl-1H-azepine-4- 4- (p-chlorobenzyl) -2- (hexahydro-1-methyl-1H-azepine-4-, characterized in that it is hydrolyzed and decarboxylated after obtaining yl) -1 (2H) -phthalazinone. Il) -1 (2H) -phthalazinone or a salt thereof. [Effect] According to the present invention, azelastine or a salt thereof can be industrially advantageously produced under mild conditions.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-102391253-A
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/KR-100426534-B1
priorityDate 1994-02-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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