Cephalosporins and their production
US4086340A · kind A · utility
Assignee
Inventors
Key dates
| Filing date | May 12, 1976 |
| Grant date | Apr 25, 1978 |
| Priority date | — |
| Expiry date | May 12, 1996 |
Classification
- Technology area (CPC C)Chemistry; Metallurgy
- CPC primaryC07D501/20
- WIPO fieldOrganic fine chemistry
- WIPO sectorChemistry
Abstract
Cephalosporins of the formula ##STR1## their pharmaceutically-acceptable, nontoxic salts, and hydrates thereof are produced, wherein PA1 A is hydrogen; unsubstituted or substituted alkyl; aryl; or R.sub.1 --X--, wherein PA1 X is --CO-- or --SO.sub.2 --, and PA1 R.sub.1 is hydrogen, unsubstituted or substituted alkyl; aryl; thienyl; furyl; amino; alkylamino; dialkylamino; pyrrolidyl; or piperidyl; Or when PA1 X is --CO--, PA1 R.sub.1 can also be alkoxy; PA1 B is phenyl, methylphenyl, chlorophenyl, hydroxyphenyl or the moiety ##STR2## E is hydrogen, hydroxyl or acetoxy; and C is a center of chirality. These compounds are particularly useful for their antimicrobial and, particularly, antibacterial effects.
Source: USPTO / EPO open patent data. Objective bibliographic and citation counts.