HRID1934839

反应详情

EQUATION

反应方程式

HRID 1934839 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

PROCEDURE

实验过程

Crude (2R-trans)-1-[[[4-chloro-5-[[(chloromethyl)sulfonyl]amino]-2-fluorophenyl]amino]carbonyl]-4-fluoro-2-pyrrolidinecarboxylic acid (173.43 g) was suspended in 550 mL of dichloromethane and 0.65 mL (0.61 g, 8.4 mmol) of N,N-dimethylformamide was added, followed by the dropwise addition of 58 mL (95 g, 0.80 mol) of thionyl chloride at room temperature, and stirring was continued at room temperature. After 2.5 hours, the mixture became homogeneous. After 22 hours, the mixture was poured into 500 mL of ice-water, the layers were separated and the aqueous layer was extracted with dichloromethane (twice with 75 mL). The organic layers were combined, washed with saturated aqueous sodium bicarbonate (twice with 400 mL), dried over magnesium sulfate and evaporated under reduced pressure to afford 140.69 g of the crude title compound (84.7% yield from the isocyanate).

WORKUP

后处理

  1. customwas continued at room temperature
  2. waitAfter 22 hours
  3. customthe layers were separated
  4. extractionthe aqueous layer was extracted with dichloromethane (twice with 75 mL)
  5. washwashed with saturated aqueous sodium bicarbonate (twice with 400 mL),
  6. dry with materialdried over magnesium sulfate
  7. customevaporated under reduced pressure