HRID241432

反应详情

EQUATION

反应方程式

HRID 241432 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

In a thermally controlled reactor, stir a mixture of 2-bromo-1-[4-(trifluoromethyl)phenyl]propan-1-one (500 g, 1.78 mol, 1 equiv), IPA (5 L), 2-aminopyrimidine (205 g, 2.13 mol, 1.2 equiv), and sodium bicarbonate (298.8 g, 3.55 mol, 2 equiv) at 80° C. for 18 hours. Cool the suspension, and concentrate in vacuo. Dilute the resulting mixture in DCM (5 L), and wash with brine (2 L). Re-extract the brine wash with DCM (2.5 L); combine all the organic phases; and dry over MgSO4; filter; and collect the filtrate. Concentrate the filtrate to dryness under reduced pressure, and slurry the resulting red gum in Et2O (1.5 L). Collect the resulting solid by filtrate, and air dry for 45 min to give the title compound as a fine, off white solid (108 g, 22% yield). MS (m/z) 278 (M+1).

WORKUP

后处理

  1. temperatureCool the suspension
  2. concentrationconcentrate in vacuo
  3. additionDilute the resulting mixture in DCM (5 L)
  4. washwash with brine (2 L)
  5. washRe-extract the brine wash with DCM (2.5 L)
  6. dry with materialand dry over MgSO4
  7. filtrationfilter
  8. customand collect the filtrate
  9. concentrationConcentrate the filtrate to dryness under reduced pressure
  10. customCollect the resulting solid by filtrate, and air
  11. customdry for 45 min