反应详情

To a cooled and stirred solution of 3-{4-[4-trifluoromethyl-6-(6-trifluoromethyl-pyridin-3-yl)-pyrimidin-2-yl]-pyridin-2-yl}-benzenesulfonic acid tert-butylamide (0.71 g) in dichloromethane (12 ml) was added TFA (12 ml) and the reaction mixture was allowed to stir at room temperature for 15 h. The mixture was evaporated to dryness, poured into 2N Na2CO3 solution (25 ml) and extracted with ethyl acetate (3×50 ml). The combined organic layers were washed with brine (50 ml), dried (MgSO4) and evaporated. Further purification by crystallization (ethyl acetate/heptane) yielded the title compound as a white solid (0.51 g, 49%). MS (ISP) 526.2 [(M+H)+]; mp 258° C.

1. temperatureTo a cooled
2. customThe mixture was evaporated to dryness
3. additionpoured into 2N Na2CO3 solution (25 ml)
4. extractionextracted with ethyl acetate (3×50 ml)
5. washThe combined organic layers were washed with brine (50 ml)
6. dry with materialdried (MgSO4)
7. customevaporated
8. customFurther purification
9. customby crystallization (ethyl acetate/heptane)