HRID509997

反应详情

EQUATION

反应方程式

HRID 509997 的结构方程式

CONDITIONS

反应条件

温度
70 °C

PROCEDURE

实验过程

Into a round bottom flask, [5-(5-chloro-1H-pyrrolo[2,3-b]pyridin-3-ylmethyl)-1-(4-methoxy-benzyl)-1H-pyrazol-3-yl]-(4-fluoro-benzyl)-amine (149, 0.060 g, 0.13 mmol) was dissolved in 5 mL of trifluoroacetic acid (60 mmol) and the reaction was heated at 70° C. overnight. The reaction was cooled to room temperature, then concentrated under vacuum and ethyl acetate was added. This was washed with 1 M aqueous potassium carbonate and brine, dried with sodium sulfate and purified by silica gel column chromatography, eluting with 2-20% methanol in dichloromethane. Appropriate fractions were combined and concentrated under vacuum, and the solid further washed with ethyl acetate and hexane to provide the desired compound. 1H NMR was consistent with compound structure. MS (ESI) [M+H+]+=356.85.

WORKUP

后处理

  1. temperatureThe reaction was cooled to room temperature
  2. concentrationconcentrated under vacuum and ethyl acetate
  3. additionwas added
  4. washThis was washed with 1 M aqueous potassium carbonate and brine
  5. dry with materialdried with sodium sulfate
  6. custompurified by silica gel column chromatography
  7. washeluting with 2-20% methanol in dichloromethane
  8. concentrationconcentrated under vacuum
  9. washthe solid further washed with ethyl acetate and hexane