HRID976278
反应详情
EQUATION
反应方程式
REACTANTS
反应物
PRODUCTS
生成物
AUXILIARIES
试剂、催化剂与溶剂
PROCEDURE
实验过程
2 g (5.0 mmol)of N-[3-(1,1,2,2-tetrafluoro-ethoxy)-phenyl]-4-(2-chloro-4-pyridyl)-2-pyrimidineamine are stirred for 44 h at 100° in 30 ml of 3-amino-1-propanol. After concentration by evaporation and chromatography (methylene chloride:methanol:conc. ammonia solution=95:5:1), N-[3-(1,1,2,2-tetrafluoro-ethoxy)-phenyl]-4-[2-(3-hydroxy-propyl-amino)-4-pyridyl]-2-pyrimidineamine is obtained; m.p. 141°-145°, MS(FAB): 438 (M+ +H), Rf =0.28 (methylene chloride:methanol:conc. ammonia solution=95:5:1).
WORKUP
后处理
- concentrationAfter concentration
- customby evaporation and chromatography (methylene chloride:methanol:conc. ammonia solution=95:5:1)