Intermediates for the preparation of beta-lactam antibiotics
US5053500A · kind A · utility
0Cited by
7References
5Claims
0Family size
Assignee
Inventors
Key dates
| Filing date | Jul 20, 1990 |
| Grant date | Oct 1, 1991 |
| Priority date | — |
| Expiry date | Jul 20, 2010 |
Classification
- Technology area (CPC Y)Emerging Cross-Sectional Technologies
- CPC primaryY02P20/55
- WIPO fieldOrganic fine chemistry
- WIPO sectorChemistry
Abstract
Cephalosporin derivatives of the formulae ##STR1## wherein X is sulphur, oxygen, methylene or sulphinyl, R3 is hydrogen or methoxy, R54 is hydrogen or a carboxyl protecting group, R.sup.51 is a (1-4C)alkyl group, R.sup.4 is hydrogen, (1-4C)alkyl, halo(1-4C)alkyl, hydroxy(1-4C)alkyl, (1-4C)alkoxy(1-4C)alkyl, carboxy (1-4C)alkyl, amino (1-4C)alkyl, cyano(1-4C)alkyl, (1-4C)alkanoylamino(1-4C)alkyl, allyl, furfuryl, benzyl or pyridyl(1-4C)alkyl and R.sup.52 is an amino protecting group and salts thereof are useful as intermediates in the preparation of cephalosporin antibiotics.
Source: USPTO / EPO open patent data. Objective bibliographic and citation counts.