HRID1423321

反应详情

EQUATION

反应方程式

HRID 1423321 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

3

CONDITIONS

反应条件

温度
80 °C

PROCEDURE

实验过程

6-fluoro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)quinoline (996.4 mg, 3.65 mmol), K3PO4 (1933.6 mg, 9.12 mmol), and PdCl2(dppf).CH2Cl2 (248 mg, 0.30 mmol) was added to a solution of 5-chloro-3-iodo-N,N-bis((2-(trimethylsilyl)ethoxy)methyl)pyrazolo[1,5-a]pyrimidin-7-amine (1684.3 mg, 3.04 mmol) in dioxane (18 mL) and H2O (3 mL). The resulting mixture was stirred at 80° C. under argon overnight. The mixture was diluted with H2O and then extracted with ethyl acetate (×2). The combined organic layers were washed with brine and dried with Na2SO4. Evaporation and purification by column chromatography afforded 5-chloro-3-(6-fluoroquinolin-3-yl)-N,N-bis((2-(trimethylsilyl)ethoxy)methyl)pyrazolo[1,5-a]pyrimidin-7-amine: LCMS tR=3.34 Min (5 min run, UV254nm), Mass calculated for, M+573.2, observed LC/MS m/z 574.2 (M+H).

WORKUP

后处理

  1. extractionextracted with ethyl acetate (×2)
  2. washThe combined organic layers were washed with brine
  3. dry with materialdried with Na2SO4
  4. customEvaporation and purification by column chromatography