Process for 3-H-3-cephem esters
US4065618A · kind A · utility
Assignee
Inventor
Key dates
| Filing date | Sep 3, 1976 |
| Grant date | Dec 27, 1977 |
| Priority date | — |
| Expiry date | Sep 3, 1996 |
Classification
- Technology area (CPC C)Chemistry; Metallurgy
- CPC primaryC07D501/59
- WIPO fieldOrganic fine chemistry
- WIPO sectorChemistry
Abstract
7-Amino-(or 7-acylamido)-3-(disubstituted-amino)-3-cephem-4-carboxylic acid esters are prepared with the corresponding 3-chloro-3-cephem ester or 3-alkyl-(or aryl)-sulfonyloxy-3-cephem esters and a secondary amine, e.g., diphenylmethyl 7-[2-(2-thienyl)acetamido]-3-morpholino-3-cephem-4-carboxylate is prepared with the corresponding 3-methyl-sulfonyloxy ester and morpholine. The 3-amino-substituted cephem esters are useful intermediates undergoing reduction with diborane to the corresponding 3H-3-cephem esters or, alternatively, they are reacted with Grignard reagents, e.g., phenylmagnesium bromide to provide, for example, the 3-phenyl-3-cephem ester.
Source: USPTO / EPO open patent data. Objective bibliographic and citation counts.