HRID253418

反应详情

EQUATION

反应方程式

HRID 253418 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

CONDITIONS

反应条件

温度
80 °C

PROCEDURE

实验过程

(4-Benzyloxy-2-fluoro-5-methoxy-phenyl)-(1-triisopropylsilanyl-1H-pyrrolo[2,3-b]pyridin-3-yl)-methanol (84, 1.49 g, 2.79 mmol) was dissolved in acetonitrile (50 mL) and trifluoroacetic Acid (1.1 mL) was added. The reaction was stirred for 5 minutes. Triethylsilane (2.2 mL) was added to the reaction. The reaction was heated at 80° C. for 6 hours. The reaction was concentrated and the crude material was dissolved into ethyl acetate and washed with 1 N HCl, saturated sodium bicarbonate, and brine. The organic portion was dried over anhydrous sodium sulfate and concentrated. The solid obtained was used in the next reaction without further purification (85, 833 mg, 83%). MS (ESI) [M+H+]+=363.4.

WORKUP

后处理

  1. concentrationThe reaction was concentrated
  2. dissolutionthe crude material was dissolved into ethyl acetate
  3. washwashed with 1 N HCl, saturated sodium bicarbonate, and brine
  4. dry with materialThe organic portion was dried over anhydrous sodium sulfate
  5. concentrationconcentrated
  6. customThe solid obtained
  7. customwas used in the next reaction without further purification (85, 833 mg, 83%)