HRID505410

反应详情

EQUATION

反应方程式

HRID 505410 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

PROCEDURE

实验过程

The title compound is synthesized according to General Procedure A. 100 mg of 2-[2-(2-amino-4-methylpyridin-6-yl)ethyl]-6-bromo-3H-imidazo[4,5-b]pyridine in 5.0 ml dioxane, 903 μl Na2CO3 solution, 78 mg of 4-benzoxyphenylboronic acid, 13 mg of PdCl2(PCy3)2, 110° C. for 70 h, 20 ml of CH2Cl2/H2O, 120 mg of crude title compound is purified by recrystallization from 5.0 ml isopropyl alcohol to yield 57 mg of the pure title compound as colorless solid. M.p. 225° C. ESI-MS: 436.3 (MH+). TLC: Rf=0.35 (dichloromethane/methanol 10:1).

WORKUP

后处理

  1. customThe title compound is synthesized
  2. custom20 ml of CH2Cl2/H2O, 120 mg of crude title compound is purified by recrystallization from 5.0 ml isopropyl alcohol