摘要 |
A process for the preparation of carbapenem-type antibacterial agents involving the following reaction: wherein R<SUP>1 </SUP>is a C<SUB>1</SUB>-C<SUB>3 </SUB>alkyl group, n is 0, 1 or 2, A is a C<SUB>1</SUB>-C<SUB>3 </SUB>alkylene group, L is a leaving group, R<SUP>3 </SUP>is a hydrogen atom, a C<SUB>1</SUB>-C<SUB>3 </SUB>alkyl group or an amino protecting group, and the hydroxyl or carboxyl groups are optionally independently protected. In such process, amine compound (1) or a salt thereof acts as a synthetic intermediate. Such process is a less expensive and highly safe synthetic route for carbapenem-type antibacterial agents suitable for large-scale synthesis.
|