HRID603926

反应详情

EQUATION

反应方程式

HRID 603926 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

3

PROCEDURE

实验过程

tert-Butyl (4-{(2R,3R)-1-(4-chlorophenyl)-3-[(3-nitropyridin-2-yl)dithio]-4-oxoazetidin-2-yl}phenoxy)acetate (Method 27) (0.70 g, 1.22 mmol) was dissolved in acetone (30 mL) at room temperature, then water (10 mL) and triphenyl phosphine (0.32 g, 1.22 mmol) was added. The mixture was stirred at room temperature for 15 minutes and then concentrated under reduced pressure to afford the crude thiol as a brown oil. This crude thiol was immediately dissolved in CH2Cl2 (30 mL) and 1-benzo[1,3]dioxol-5-yl-2-bromo-ethanone (0.59 g, 2.44 mmol) was added, followed by Et3N (0.34 mL, 2.44 mmol). The mixture was stirred at room temperature for 18 hours, concentrated under reduced pressure and purified by flash-chromatography (Heptane:EtOAc 7:3 and then 2:1). The resulting product (0.90 g) was dissolved in 15 ml formic acid and stirred at room temperature for 3 hours. Concentration under reduced pressure and purification by flash-chromatography afforded the title compound.

WORKUP

后处理

  1. concentrationconcentrated under reduced pressure
  2. customto afford the crude thiol as a brown oil
  3. stirringThe mixture was stirred at room temperature for 18 hours
  4. concentrationconcentrated under reduced pressure
  5. custompurified by flash-chromatography (Heptane:EtOAc 7:3
  6. dissolutionThe resulting product (0.90 g) was dissolved in 15 ml formic acid
  7. stirringstirred at room temperature for 3 hours
  8. concentrationConcentration
  9. customunder reduced pressure and purification by flash-chromatography