HRID2366856

反应详情

EQUATION

反应方程式

HRID 2366856 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

CONDITIONS

反应条件

温度
80 °C

PROCEDURE

实验过程

4-bromo-1-(2-chloroethyl)-1H-pyrazole (317 mg, 1.513 mmol, for a preparation see Intermediate 54) was dissolved in N,N-dimethylformamide (DMF) (5 mL) and cesium carbonate (740 mg, 2.270 mmol) added with N-methyl-1-phenylmethanamine (0.973 mL, 7.57 mmol, available from Aldrich). The mixture was heated to 80° C. for 3 hours then allowed to stir at 80° C. overnight. The mixture was cooled to room temperature and loaded on to a 20 g SCX cartridge. The SCX was eluted with MeOH (100 ml) and 2M methanolic ammonia (100 ml). The basic fraction was evaporated to a colourless oil, loaded on to a 25+M Biotage silica column and eluted with a gradient of 0 to 2.5% 2M methanolic ammonia in DCM. The product containing fractions were evaporated to a pale yellow oil (155 mg). LCMS (Method C): Rt=0.67, MH+=294

WORKUP

后处理

  1. temperatureThe mixture was cooled to room temperature
  2. washThe SCX was eluted with MeOH (100 ml) and 2M methanolic ammonia (100 ml)
  3. customThe basic fraction was evaporated to a colourless oil
  4. washeluted with a gradient of 0 to 2.5% 2M methanolic ammonia in DCM
  5. additionThe product containing fractions
  6. customwere evaporated to a pale yellow oil (155 mg)