Predicate |
Object |
assignee |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_f88f84fc279fe5d0b9b5ec3c88c2e2b2 |
classificationCPCInventive |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D213-75 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D247-02 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D471-04 |
classificationIPCInventive |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D471-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D405-12 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D213-75 |
filingDate |
1987-04-13-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
grantDate |
1988-06-07-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
inventor |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_867a3a71ba36939514b3a50860cb388f http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_322feee405794c458c99fb427506077b |
publicationDate |
1988-06-07-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber |
US-4749788-A |
titleOfInvention |
Process for the preparation of aryl-pyrido(1,4) benzodiazepines |
abstract |
A process is described wherein pyrido[1,4]benzodiazepines having the formula: ##STR1## wherein Q is NR 1 R 2 or ##STR2## are prepared from unsubstituted pyridobenzodiazepinones by alkylation reaction with halo-alkyl-Q followed by acylation of the other nitrogen; breaking the ring with an aryl Grignard reagent and recyclizing to add the aryl radical and form the azepine ring. Novel intermediates are thereby disclosed. |
isCitedBy |
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-5006522-A http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-5264432-A |
priorityDate |
1987-04-13-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type |
http://data.epo.org/linked-data/def/patent/Publication |