HRID563946

反应详情

EQUATION

反应方程式

HRID 563946 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

3

PROCEDURE

实验过程

To a solution of 3-bromopyridine (4.75 gm, 30 mmol) and 3-aminopyridine (1.88 gm, 20 mmol) in dry toluene (8 mL) was added sodium t-butoxide (2.3 gm, 24 mmol), tris(dibenylideneacetone) dipalladium(0) (63 mg, 0.069 mmol), and 9,9-dimethyl-4,5-bis(diphenylphosphino)xanthene (XANTPHOS) (183 mg, 0.317 mmol). The vessel was capped with a septum, degassed (3×), and heated at 100 C for ˜24 hours. The cooled reaction was diluted with methylene chloride, washed with NaHCO3 solution, water, and the organic layer dried over anhydrous sodium sulfate, filtered and the solvent concentrated to a small volume. Upon addition of diethyl ether and a few drops of methanol the product precipitated. After stirring this mixture for ˜15 hours the purified product was isolated by filtration to give 2.89 gm (84% yield) of the title compound.

WORKUP

后处理

  1. customThe vessel was capped with a septum
  2. customdegassed (3×)
  3. temperatureheated at 100 C for ˜24 hours
  4. customThe cooled reaction
  5. washwashed with NaHCO3 solution, water
  6. dry with materialthe organic layer dried over anhydrous sodium sulfate
  7. filtrationfiltered
  8. concentrationthe solvent concentrated to a small volume
  9. additionUpon addition of diethyl ether and a few drops of methanol the product
  10. customprecipitated
  11. customwas isolated by filtration