Réaction #55411
ord-2b641d84180448b3873fe599834e67dc
Équation de réaction
Réactifs
Réactifs
Solvants
Conditions de réaction
Traitement
- 1workup.ADDITIONA suspension of 3.85 g
- 2AutreThe reaction mixture was evaporated to dryness and water and ethyl acetate
- 3workup.ADDITIONwere added to the residue
- 4AutreThe layers were separated
- 5workup.ADDITIONethyl acetate was added to the aqueous phase and it
- 6workup.ADDITIONwas acidified to pH 2.5 by addition of 6N hydrochloric acid
- 7FiltrationThe mixture was filtered
- 8Autrethe layers were separated
- 9Extractionthe aqueous phase was extracted with ethyl acetate
- 10LavageThe extract was washed with water
- 11Séchagedried (MgSO4)
- 12Autreevaporated to dryness
Mode opératoire
A suspension of 3.85 g. (0.01 mol.) of 7-amino-3-[1-(2-carbamoylethyl)tetrazol-5-ylthiomethyl]-3-cephem-4-carboxylic acid in 50 ml. of dry dimethylformamide was treated with 2 ml. of triethylamine and the mixture was stirred for 15 minutes at 25°. The activated ester of trifluoromethylmercaptoacetic acid (2.57 g., 0.016 mol.) was added to the mixture and it was stirred an additional hour. The reaction mixture was evaporated to dryness and water and ethyl acetate were added to the residue. The layers were separated, ethyl acetate was added to the aqueous phase and it was acidified to pH 2.5 by addition of 6N hydrochloric acid. The mixture was filtered, the layers were separated and the aqueous phase was extracted with ethyl acetate. The extract was washed with water, dried (MgSO4) and evaporated to dryness to give the title compound.