HRID389044

反应详情

EQUATION

反应方程式

HRID 389044 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

CONDITIONS

反应条件

温度
80 °C

PROCEDURE

实验过程

3-Chloro-6-(4-cyclopropylpiperazin-1-yl)pyridazine (8.0 g, 33.5 mmol), acetonitrile (100 mL), 1 M sodium carbonate solution (100.5 mL, 100.5 mmol) and bis(triphenylphosphine)palladium(II) chloride (1.17 g, 1.67 mmol) were mixed and degassed in vacuo under nitrogen. 3,4-Methylenedioxybenzeneboronic acid (8.34 g, 50.3 mmol) was added and the mixture was heated to 80° C. for 16 h. The precipitated product was filtered and washed with acetonitrile and water, and dried in vacuo. The solid was suspended in methanol (500 mL) and 2,2 equivalents of a 4M HCl in dioxane solution was added. The formed solution was filtered, concentrated in vacuo and acetonitrile (100 mL) was added. The suspension was stirred for 1 h, filtered and the solid dried in vacuo to yield 3-(1,3-benzodioxol-5-yl)-6-(4-cyclopropylpiperazin-1-yl)pyridazine as a yellow powder, 11.4 g, 86%.

WORKUP

后处理

  1. customdegassed in vacuo under nitrogen
  2. filtrationThe precipitated product was filtered
  3. washwashed with acetonitrile and water
  4. customdried in vacuo
  5. addition2,2 equivalents of a 4M HCl in dioxane solution was added
  6. filtrationThe formed solution was filtered
  7. concentrationconcentrated in vacuo and acetonitrile (100 mL)
  8. additionwas added
  9. filtrationfiltered
  10. customthe solid dried in vacuo