反应详情

To a suspension of 7β-amino-3-methanesulfonyloxy-3-cephem-4-carboxylic acid diphenylmethyl ester hydrochloride (1.49 g: 3 mMol.) and (Z)-2-(2-t-butoxycarbonylaminothiazol-4-yl)-2-pentenoic acid (1.03 g: 3.45 mMol.) in dichloromethane (30 ml) is added at -30° C. N-methylmorpholine (1.1 ml : 10 mMol.) and, after 2 minutes, phenyl dichlorophosphate (0.49 ml: 3.27 mMol.), and the mixture is stirred at the same temperature for 1 hour and 20 minutes. The reaction mixture is mixed with 1N-hydrochloric acid (6 ml) and extracted with ethyl acetate. The extract is washed with water, aqueous 5% sodium hydrogen carbonate, and brine, dried over sodium sulfate, and concentrated. The residue (2.6 g) is dissolved in hot isopropanol (100 ml), cooled, and the separating pale yellow powder is collected by filtration to give 7β-[(Z)-2-(2-t-butoxycarbonylaminothiazol-4-yl)-2-pentenoylamino]-3-methanesulfonyloxy-3-cephem-4-carboxylic acid diphenylmethyl ester (2.01 g). Yield: 91%.

1. additionis added at -30° C
2. extractionextracted with ethyl acetate
3. washThe extract is washed with water, aqueous 5% sodium hydrogen carbonate, and brine
4. dry with materialdried over sodium sulfate
5. concentrationconcentrated
6. dissolutionThe residue (2.6 g) is dissolved in hot isopropanol (100 ml)
7. temperaturecooled
8. filtrationthe separating pale yellow powder is collected by filtration