http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CH-505842-A
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_d629f98a51b15993f56f9e04fdea237f |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C08G59-245 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C08G59-24 |
| filingDate | 1967-01-11-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_00fff36a2a59161fedda0f8b8b6d1307 |
| publicationDate | 1971-04-15-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | CH-505842-A |
| titleOfInvention | Process for the preparation of new 1,4-benzodiazepines or their 4-oxides |
| abstract | derivatives of the general formula (I), and N-trifluoroethyl substituted amino-benzophenones and anilines used as intermediates for the preparation of (I) (see "Preparation"). where X and Y = H, halogen, trifluoromethyl, nitro, alkyl or alkoxy. R1 and R2 = H, alkyl or free or esterified hydroxy, pref. an alkanoyloxy group. If R1 or R2 is a free or esterified hydroxy, the other is a hydrogen atom and the compound exists as the 4-oxide if R1 or R2 independently of each other are hydrogen or alkyl. The compounds have CNS activity, acting as tranquillisers and are not so toxic at the active dose as previously used medicines in this filed. |
| priorityDate | 1966-01-14-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 83.