HRID40844

反应详情

EQUATION

反应方程式

HRID 40844 的结构方程式

PROCEDURE

实验过程

(R)-tert-butyl 4-(1-aminoethyl)piperidine-1-carboxylate (43.82 mg, 0.19 mmol) was added to a solution of 2-(perfluorophenoxy)-4-(1-tosyl-5-(trifluoromethyl)-1H-pyrrolo[2,3-b]pyridin-3-yl)pyrimidine-5-carbonitrile (100 mg, 0.16 mmol) and the reaction mixture was stirred at room temperature for 2 hours. The crude mixture was concentrated to dryness and the resulting residue was purified on silica gel by flash column chromatography to afford the title compound (70 mg, 65% yield).

WORKUP

后处理

  1. concentrationThe crude mixture was concentrated to dryness
  2. customthe resulting residue was purified on silica gel by flash column chromatography