HRID1926069

反应详情

EQUATION

反应方程式

HRID 1926069 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

CONDITIONS

反应条件

温度
60 °C

PROCEDURE

实验过程

A mixture of tert-butyl {2-[4-({3-chloro-4-[3-(trifluoromethyl)phenoxy]phenyl}amino)-5H-pyrrolo[3,2-d]pyrimidin-5-yl]ethyl}carbamate (1.12 g), 2N hydrochloric acid (15 mL) and tetrahydrofuran (30 mL) was stirred at 60° C. for 20 hrs. The solvent was evaporated under reduced pressure, ethanol was added, and the mixture was further concentrated. The precipitated crystals were collected by filtration and the crystals were washed with ethyl acetate to give the title compound (1.07 g) as pale-yellow crystals.

WORKUP

后处理

  1. customThe solvent was evaporated under reduced pressure, ethanol
  2. additionwas added
  3. concentrationthe mixture was further concentrated
  4. filtrationThe precipitated crystals were collected by filtration
  5. washthe crystals were washed with ethyl acetate