7-phenyl-1, 4-diazepane compounds, process for their preparation, and pharmaceutical compositions containing them
US6040303A · kind A · utility
Assignee
Inventors
Key dates
| Filing date | Aug 27, 1998 |
| Grant date | Mar 21, 2000 |
| Priority date | — |
| Expiry date | Aug 27, 2018 |
Classification
- Technology area (CPC Y)Emerging Cross-Sectional Technologies
- CPC primaryY02P20/55
- WIPO fieldPharmaceuticals
- WIPO sectorChemistry
Abstract
Neurokinin-antagonistic compounds corresponding to formula I: ##STR1## in which R.sup.1 is hydrogen or lower alkyl, PA1 R.sup.2 is hydrogen, lower alkyl, lower alkoxy, halogen or trifluoromethyl, and PA1 R.sup.3 is hydrogen, lower alkyl, lower alkoxy, halogen or trifluoromethyl, or PA1 R.sup.2 and R.sup.3 together are alkylenedioxy with 1 to 2 carbon atoms, bonded to adjacent carbon atoms of the phenyl ring, PA1 R.sup.4 is hydrogen, lower alkyl, lower alkoxy, halogen or trifluoromethyl, and PA1 R.sup.5 is hydrogen, lower alkyl, lower alkoxy, halogen or trifluoromethyl, or PA1 R.sup.4 and R.sup.5 together are alkylenedioxy with 1 to 2 carbon atoms, bonded to adjacent carbon atoms of the phenyl ring, PA1 R.sup.6 is lower alkyl, halogen or trifluoromethyl, PA1 R.sup.7 is lower alkyl, halogen or trifluoromethyl, PA1 A is a --(CH.sub.2).sub.n -- group in which n represents an integer from 1 to 3, or an --NH--(CH.sub.2).sub.m -- group in which m represents an integer from 2 to 3, and PA1 B is an alkylene chain with 1 to 3 carbon atoms optionally substituted by lower alkyl, and physiologically acceptable salts thereof and processes for the preparation of these compounds.
Source: USPTO / EPO open patent data. Objective bibliographic and citation counts.