HRID1843628

反应详情

EQUATION

反应方程式

HRID 1843628 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

CONDITIONS

反应条件

温度
70 °C

PROCEDURE

实验过程

100 mg (0.16 mmol) of 1-(3-{4-[2-(tert-butylamino)pyridin-4-yl]-1-(4-methoxybenzyl)-1H-pyrazol-3-yl}phenyl)-3-[4-(trifluoromethyl)phenyl]urea were dissolved in 5 ml of trifluoroacetic acid and the mixture heated at 70° C. under stirring. After 16 hours the solution was poured into icy water, neutralized with aqueous NaHCO3 and extracted with dichloromethane. The organic layer was then dried over Na2SO4 and evaporated to dryness. The product was purified by chromatography on a silica gel column eluted with dichloromethane-methanol (gradient from 1% to 5%) obtaining 50 mg (71% yield) of the title compound.

WORKUP

后处理

  1. extractionextracted with dichloromethane
  2. dry with materialThe organic layer was then dried over Na2SO4
  3. customevaporated to dryness
  4. customThe product was purified by chromatography on a silica gel column
  5. washeluted with dichloromethane-methanol (gradient from 1% to 5%)