HRID1829174

反应详情

EQUATION

反应方程式

HRID 1829174 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

CONDITIONS

反应条件

温度
140 °C

PROCEDURE

实验过程

Copper (I) iodide (6.4 g, 33.3 mmol), potassium carbonate (6.3 g, 45.4 mmol) and 6-bromo-2-(dimethylamino)pyridine (WO 9843971) (9 g, 45.4 mmol) were added consecutively to a solution of (5S)-5-(3,4-dichlorophenyl)-5-(1,3-dioxolan-2-ylmethyl)-2-piperidinone (WO 9807722) (10 g, 30.3 mmol), in 1-methyl-2-pyrrolidinone (50 ml), and the mixture was stirred at 140° C. for 4 hours. The cooled mixture was poured into 4N hydrochloric acid, then carefully basified using 10% aqueous ammonia. The aqueous mixture was extracted with ethyl acetate (3×200 ml), and the combined organic extracts were washed with brine, dried (MgSO4) and evaporated under reduced pressure to give an orange oil. The crude product was purified by column chromatography on silica gel using methanol:dichloromethane (5:95) as eluant, and repeated using ethyl acetate as eluant. The product was treated with 1N ethereal hydrochloric acid, and evaporated under reduced pressure to afford the title compound.

WORKUP

后处理

  1. extractionThe aqueous mixture was extracted with ethyl acetate (3×200 ml)
  2. washthe combined organic extracts were washed with brine
  3. dry with materialdried (MgSO4)
  4. customevaporated under reduced pressure
  5. customto give an orange oil
  6. customThe crude product was purified by column chromatography on silica gel
  7. additionThe product was treated with 1N ethereal hydrochloric acid
  8. customevaporated under reduced pressure