反应详情
EQUATION
反应方程式
REACTANTS
反应物
PRODUCTS
生成物
AUXILIARIES
试剂、催化剂与溶剂
PROCEDURE
实验过程
A solution of phosphorous pentachloride (0.380 g, 1.8 mmol) in dichloromethane (9.5 ml) was added to t-butyl (6R,7R)-3-[(4RS)-2-oxotetrahydrofuran-4-yl]-7-phenoxyacetamidoceph-3-em-4-carboxylate (0.554 g, 1.2 mmol) and N-methylmorpholine (265 μh, 2.4 mmol) in dichloromethane (15 ml) at <-20° C. under argon. Stirred 0.5 h at -15°±5° C. then methanol (3.5 ml) added, stirred 0.75 h then water (10 ml) added and stirred vigorously 1 h. The dichloromethane was removed in vacuo. ethyl acetate added and the aqueous layer adjusted to pH7 with dilute ammonium hydroxide and extracted twice with ethyl acetate. The extracts were washed with brine, dried, concentrated and flash chromatographed on silica gel eluting with 40,50,60,70,75% ethyl acetate in hexane to provide the title compound as a foam (0.120 g, 29%): (Found: M+, 340.1113. C15H20N2O5S requires M, 340.1093); νmax (CH2Cl2) 1775, 1715, 1367, 1155 cm-1 ; δH (250 MHz, CDCl3) 1.54 (9H, s , 1.97 (2H, bs), 2.35-2.95 (2H, m), 3.26 and 3.49 3.28 and 3.49 (2H, 2ABq, J 17.7 Hz), 4.0-4.45 (3H, m), 4.77, 4.79 (1H, 2d, J 4.7 Hz), 4.93, 4.95 (1H, 2d, J 4.7 Hz).
WORKUP
后处理
- stirringstirred 0.75 h
- stirringstirred vigorously 1 h
- customThe dichloromethane was removed in vacuo
- additionethyl acetate added
- extractionextracted twice with ethyl acetate
- washThe extracts were washed with brine
- customdried
- concentrationconcentrated
- customflash chromatographed on silica gel eluting with 40,50,60,70,75% ethyl acetate in hexane