HRID1890969

反应详情

EQUATION

反应方程式

HRID 1890969 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

PROCEDURE

实验过程

To a microwave vessel was added 3-bromo-6-(6-methyl-[1,2,4]triazolo[4,3-b]pyridazin-3-ylsulfanyl)-quinoline (200 mg, 0.54 mmol), 1-ethyl-4-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-1H-pyrazole (149 mg, 0.67 mmol), K2CO3 (186 mg, 1.34 mmol), 1,4-dioxane (7 mL) and water (3.5 mL). The solution was degassed by bubbling nitrogen for 10 min and then Pd(dppf)2Cl2 dichloromethane (20 mg, 0.0269 mmol) was added. The microwave vessel was capped and reacted in a microwave reactor at 120° C. for 20 min. The microwave vessel was cooled and then the mixture was extracted into dichloromethane and washed with water. The volatiles were removed in vacuo and the residue absorbed onto silica gel and purified by flash chromatography (SiO2, dichloromethane:CH3OH 100:0-80:20) to obtain 3-(1-ethyl-1H-pyrazol-4-yl)-6-(6-methyl-[1,2,4]triazolo[4,3-b]pyridazin-3-ylsulfanyl)-quinoline as a brown oil (7% yield).

WORKUP

后处理

  1. customThe solution was degassed
  2. customby bubbling nitrogen for 10 min
  3. customThe microwave vessel was capped
  4. customreacted in a microwave reactor at 120° C. for 20 min
  5. temperatureThe microwave vessel was cooled
  6. extractionthe mixture was extracted into dichloromethane
  7. washwashed with water
  8. customThe volatiles were removed in vacuo
  9. customthe residue absorbed onto silica gel
  10. custompurified by flash chromatography (SiO2, dichloromethane:CH3OH 100:0-80:20)