HRID409094

反应详情

EQUATION

反应方程式

HRID 409094 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

CONDITIONS

反应条件

温度
25 °C

PROCEDURE

实验过程

Into a 100 mL round-bottom flask, was placed a solution of tert-butyl (3R)-3-[4-amino-3-[4-(2,6-difluorophenoxy)phenyl]-1H-pyrazolo[3,4-d]pyrimidin-1-yl]piperidine-1-carboxylate (450 mg, 0.86 mmol, 1.00 equiv) in dichloromethane (40 mL). CF3COOH (10 mL) to added dropwise with stirring at 25° C. over 10 min and the resulting solution was stirred for 3 h at 25° C. and then concentrated under vacuum. The resulting solution was diluted with dichloromethane and washed with aqueous sodium bicarbonate and brine. The organics were dried over anhydrous sodium sulfate and concentrated under vacuum to give 410 mg of 3-[4-(2,6-difluorophenoxy)phenyl]-1-[(3R)-piperidin-3-yl]-1H-pyrazolo[3,4-d]pyrimidin-4-amine as a white solid.

WORKUP

后处理

  1. customInto a 100 mL round-bottom flask, was placed
  2. stirringthe resulting solution was stirred for 3 h at 25° C.
  3. concentrationconcentrated under vacuum
  4. additionThe resulting solution was diluted with dichloromethane
  5. washwashed with aqueous sodium bicarbonate and brine
  6. dry with materialThe organics were dried over anhydrous sodium sulfate
  7. concentrationconcentrated under vacuum