HRID1989671
反应详情
EQUATION
反应方程式
REACTANTS
反应物
PRODUCTS
生成物
CONDITIONS
反应条件
- 温度
- 23 °C
PROCEDURE
实验过程
To N-tert-butyl-3-{6-[4-trifluoromethyl-6-(4-trifluoromethyl-phenyl)-pyrimidin-2-yl]-pyridin-2-yl}-benzenesulfonamide (example 362) (0.232 g, 0.40 mmol) was added TFA (3 mL) and the reaction mixture was stirred at 23° C. for 16 h. The mixture was evaporated to dryness and partitioned between EtOAc and saturated NaHCO3 solution, the organic layer was dried over Na2SO4. Removal of the solvent in vacuum left a crude product which was triturated with diethyl ether to give the title compound as a white solid (0.170 g, 81%). MS (ISP) 524.8 [(M+H)+]; mp 244° C. (dec.).
WORKUP
后处理
- customThe mixture was evaporated to dryness
- custompartitioned between EtOAc and saturated NaHCO3 solution
- dry with materialthe organic layer was dried over Na2SO4
- customRemoval of the solvent in vacuum
- waitleft a crude product which
- customwas triturated with diethyl ether