HRID332641

反应详情

EQUATION

反应方程式

HRID 332641 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

PROCEDURE

实验过程

(R)-8-(Benzyloxy)-5-(2-bromo-1-(tert-butyldimethylsilyloxy)ethyl)quinolin-2(1H)-one (5.0 g, 10.2 mmol) was dissolved in dimethyl formamide (90 mL) and water (10 mL). Sodium iodide (1.7 g, 11.3 mmol) and sodium azide (0.7 g, 11.3 mmol) were added sequentially. The reaction mixture was stirred at RT until all the solid was in solution. The solution was heated at 80° C. for 40 hours and then cooled to RT and diluted with water (300 mL). The aqueous layer was extracted with DCM, and the combined organic extracts were dried (magnesium sulfate), filtered, and concentrated under reduced pressure. The crude residue was recrystallised from ethyl acetate and iso-hexane to afford the desired compound (3.6 g, 78%), which was used without further purification in the next step.

WORKUP

后处理

  1. temperatureThe solution was heated at 80° C. for 40 hours
  2. temperaturecooled to RT
  3. extractionThe aqueous layer was extracted with DCM
  4. dry with materialthe combined organic extracts were dried (magnesium sulfate)
  5. filtrationfiltered
  6. concentrationconcentrated under reduced pressure
  7. customThe crude residue was recrystallised from ethyl acetate and iso-hexane