HRID447071

反应详情

EQUATION

反应方程式

HRID 447071 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

CONDITIONS

反应条件

温度
110 °C

PROCEDURE

实验过程

To a round bottom flask is added 3-chloro-4,5-dimethyl-6-((R)-3-methyl-piperazin-1-yl)-pyridazine (500 mg, 2.07 mmol), 4-fluorophenylboronic acid (580 mg, 4.15 mmol) sodium carbonate (440 mg, 4.15 mmol), toluene (16 mL) and water (8 mL). The reaction mixture is purged with nitrogen for 20 min. Tetrakis(triphenylphosphine) palladium (50 mg, 0.103 mmol) is added and the mixture is heated to 110° C. for 18 h. The reaction mixture is concentrated and partitioned between ethylacetate and water. It is extracted with ethylacetate twice and the combined organic phases are dried with sodium sulfate and concentrated. It is purified by column chromatography (0-25% methanol/methylene chloride) to give 480 mg of 3-(4-fluoro-phenyl)-4,5-dimethyl-6-((R)-3-methyl-piperazin-1-yl)-pyridazine (83%).

WORKUP

后处理

  1. customThe reaction mixture is purged with nitrogen for 20 min
  2. concentrationThe reaction mixture is concentrated
  3. custompartitioned between ethylacetate and water
  4. extractionIt is extracted with ethylacetate twice
  5. dry with materialthe combined organic phases are dried with sodium sulfate
  6. concentrationconcentrated
  7. customIt is purified by column chromatography (0-25% methanol/methylene chloride)