http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-H06271547-A
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_01249be6ad92a1f01c99b5987ca16162 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D237-32 |
| filingDate | 1993-03-22-04:00^^<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 | 1994-09-27-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | JP-H06271547-A |
| titleOfInvention | 4- (p-chloro-1-cyanobenzyl) -1 (2H) -phthalazinone and process for producing the same |
| abstract | (57) [Summary] [Structure] 1,4-dichlorophthalazine represented by the following formula (II) is reacted with 4-chlorobenzylanide represented by the following formula (III) to obtain the following formula (IV): After synthesizing I-chloro-4- (p-chloro-1-cyanobenzyl) -phthalazine shown below, 4- (p-chloro-1-cyanobenzyl) represented by the following formula (I) is obtained by hydrolysis. -1 (2H) -phthalazinone is prepared. [Chemical 1] [Effect] The compound of the above formula (I) is 4- (p-chlorobenzyl) -2- (hexahydro-1-methyl-1). H-azepin-4-yl) -1 (2H) -phthalazinone It can be effectively used as a synthetic intermediate of a phthalazinone derivative which is effective as a medicine such as hydrochloride . |
| priorityDate | 1993-03-22-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 42.