HRID1416963

反应详情

EQUATION

反应方程式

HRID 1416963 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

3

PROCEDURE

实验过程

To a mixture of 0.1 g (0.23 mmol) of 2-bromo-6-(4-fluorophenyl)-5-[4-(methylsulfonyl)phenyl]-pyridine-3-carbonitrile (Example 3), 10 ml of toluene and 4 ml of ethanol was added 34 mg (0.28 mMol) of phenylboric acid and a solution of 71 mg (0.52 mMol) of K2CO3 in 1 ml water. To the resulting reaction mixture was added 18 mg of tetrakis(triphenylphosphine)palladium. The mixture was held at reflux overnight, cooled to room temperature, poured into 75 ml of water and extracted with dichloromethane. The combined organic solutions were washed once with 10% NaOH solution, once with brine, dried over MgSO4 and evaporated to dryness to give a yellowish oil which crystallized upon standing. Trituration with ether gave 74.5 mg (76%) of a white powder: m.p. 230-231° C.

WORKUP

后处理

  1. customTo the resulting reaction mixture
  2. temperatureat reflux overnight
  3. extractionextracted with dichloromethane
  4. washThe combined organic solutions were washed once with 10% NaOH solution, once with brine
  5. dry with materialdried over MgSO4
  6. customevaporated to dryness
  7. customto give a yellowish oil which
  8. customcrystallized