反应详情
EQUATION
反应方程式
REACTANTS
反应物
PRODUCTS
产物
AUXILIARIES
试剂、催化剂与溶剂
CONDITIONS
反应条件
- 温度
- 0 °C
PROCEDURE
实验过程
Isobutylchloroformate (0.17 mL, 1.33 mmol) was added to a solution of Example 72k (0.40 g, 0.88 mmol) in dry CH2Cl2 (15 mL). Triethylamine (0.23 ml, 1.67 mmol) was added and the reaction mixture was stirred at 0° C. for 1 h. It was brought to room temperature, treated with water and extracted with chloroform. The organic layer was washed with water, brine, dried, concentrated and crystallised using ethyl acetate to obtain the title compound as a white solid. Yield: 0.280 g, (58%). 1H NMR (DMSO-d6): δ 0.80 (d, 6H, 2CH3), 1.70-1.80 (m, 5H, 2CH2, CH), 2.50-2.89 (m, 11H, 4CH2, CH3), 3.90 (d, 2H, CH2), 5.19 (s, 2H, CH2), 7.55 (s, 1H, Ar), 7.75 (s, 1H, Ar), 8.10 (s, 1H, Ar), 8.20 (s, 1H, Ar). MS: m/e (EI+) 565 (M+).
WORKUP
后处理
- customwas brought to room temperature
- extractionextracted with chloroform
- washThe organic layer was washed with water, brine
- customdried
- concentrationconcentrated
- customcrystallised