HRID479946

反应详情

EQUATION

反应方程式

HRID 479946 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

CONDITIONS

反应条件

温度
50 °C

PROCEDURE

实验过程

To a solution of Benzyl-[1-(4-fluoro-benzenesulfonyl)-azetidin-3-yl]-carbamicacid tert-butyl ester (0.21 g, 0.5 mmol) in N,N′-dimethylpropyleneurea (0.5 ml) was added butylamine (0.15 g, 2 mmol) and potassium carbonate (0.07 g, 0.5 mmol), and the mixture was stirred at 50° C. for 2 days. It was then cooled to room temperature and diluted with water (20 ml). The aqueous phase was removed, and the residue dissolved in ether (20 ml). The ether solution was washed with 0.5 N HCl, saturated sodium bicarbonate solution, and brine, and dried over anhydrous sodium sulfate. It was then filtered through a pad of silica gel. The filtrate was evaporated, and the residue was triturated with hexanes to give 0.23 g of a white solid; m.p. 115-116° C.; MS (ES) m/z 474.1 (MH+); HRMS (EI) Calcd. for C25H35N3O4S (M+): 473.2348, Found: 473.2338.

WORKUP

后处理

  1. temperatureIt was then cooled to room temperature
  2. customThe aqueous phase was removed
  3. dissolutionthe residue dissolved in ether (20 ml)
  4. washThe ether solution was washed with 0.5 N HCl, saturated sodium bicarbonate solution, and brine
  5. dry with materialdried over anhydrous sodium sulfate
  6. filtrationIt was then filtered through a pad of silica gel
  7. customThe filtrate was evaporated
  8. customthe residue was triturated with hexanes