Diazepine derivatives
US4382032A · kind A · utility
Assignee
Inventors
Key dates
| Filing date | Jul 30, 1982 |
| Grant date | May 3, 1983 |
| Priority date | — |
| Expiry date | Jul 30, 2002 |
Classification
- Technology area (CPC Y)Emerging Cross-Sectional Technologies
- CPC primaryY02A50/30
- WIPO fieldPharmaceuticals
- WIPO sectorChemistry
Abstract
There is presented imidazodiazepines of the formula ##STR1## wherein A together with the two carbon atoms denoted as .alpha. and .beta. is the group ##STR2## R.sup.1 is hydrogen, lower alkyl, lower alkoxymethyl, halogen, nitro or a group of the formula --COOR.sup.4, R.sup.2 is hydrogen, trifluoromethyl or halogen, PA1 R.sup.3 is hydrogen, trifluoromethyl, halogen or lower alkyl, R.sup.4 is methyl, ethyl or isopropyl and X is an oxygen or sulphur atom and the carbon atom denoted as .gamma. has the (S)-- or (R,S)-- configuration, and their pharmaceutically acceptable acid addition salts. The compounds are useful in the antagonization of the central-depressant, muscle relaxant, ataxic, blood pressure-lowering and respiratory-depressant properties of 1,4-benzodiazepines which have tranquillizing activity. They can also be used for suppressing the activities on the central nervous system of 1,4-benzodiazepines used in other fields of therapy, for example, of schistosomicidally-active 1,4-benzodiazepines. Also provided are methods to produce the above compounds.
Source: USPTO / EPO open patent data. Objective bibliographic and citation counts.