Reaction #4866
ord-29e2e1d3d5724c9c82294db3f2de9b86
Reaction equation
Reactants
Reagents
Solvents
Conditions
Workup
- 1FiltrationInsoluble materials are filtered off
- 2Concentrationthe filtrate is concentrated to dryness under reduced pressure
- 3workup.DISSOLUTIONThe residue is dissolved in ethyl acetate
- 4Washwashed with 1% hydrochloric acid, 5% aqueous sodium bicarbonate solution
- 5DryingThe ethyl acetate solution is then dried
- 6Concentrationconcentrated to dryness under reduced pressure
- 7OtherThe residue thus obtained
- 8Otheris purified by silica gel chromatography (solvent, ethyl acetate:benzene=5:2)
Procedure
3.25 g of (Z)-2-(2-tritylaminothiazol-4-yl)-2-[(2-pyrrolidon-3-yl)oxyimino]acetic acid are dissolved in 200 ml of tetrahydrofuran, and 3.14 g of benzhydryl 7β-amino-3-[(1-methyl-1H-tetrazol-5-yl)thiomethyl]-3-cephem-4-carboxylate, 1.03 g of 1-hydroxybenzotriazole and 1.57 g of dicyclohexylcarbodiimide are added thereto. The mixture is stirred at room temperature for 2 hours. Insoluble materials are filtered off, and the filtrate is concentrated to dryness under reduced pressure. The residue is dissolved in ethyl acetate, and washed with 1% hydrochloric acid, 5% aqueous sodium bicarbonate solution and an aqueous saturated sodium chloride solution, successively. The ethyl acetate solution is then dried and concentrated to dryness under reduced pressure. The residue thus obtained is purified by silica gel chromatography (solvent, ethyl acetate:benzene=5:2). 3.7 g of benzhydryl 7β-{(Z)-2-(2-tritylaminothiazol-4-yl)-2-[(2-pyrrolidon-3-yl)oxyimino]acetamido}-3-[(1-methyl-1H-tetrazol-5-yl)thiomethyl]- 3-cephem-4-carboxylate are obtained.