HRID1755365

反应详情

EQUATION

反应方程式

HRID 1755365 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

3

CONDITIONS

反应条件

温度
100 °C

PROCEDURE

实验过程

A mixture of (S)-6-chloro-N-(6-(2-methylpyrrolidin-1-yl)pyridin-2-yl)imidazo[1,2-b]pyridazin-8-amine (0.08 g, 0.243 mmol), 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoic acid (0.066 g, 0.268 mmol), Pd2(dba)3 (0.028 g, 0.049 mmol), X-phos (0.046 g, 0.097 mmol) and Na2CO3 (0.103 g, 0.992 mmol) in dioxane (20 mL) and water (5 mL) was heated to 100° C. for 16 h in a sealed tube under N2 atmosphere then concentrated in vacuo. The residue was purified by chromatography (silica gel, 15 g, 200-300 mesh, MeOH:dichloromethane=1:10) to afford (S)-4-(8-(6-(2-methylpyrrolidin-1-yl)pyridin-2-ylamino)imidazo[1,2-b]pyridazin-6-yl)benzoic acid (90 mg) as a yellow solid. LC-MS: [M+1]+=415, tR=1.660 min. This contained unidentified impurities and was used directly without further purification.

WORKUP

后处理

  1. concentrationthen concentrated in vacuo
  2. customThe residue was purified by chromatography (silica gel, 15 g, 200-300 mesh, MeOH:dichloromethane=1:10)