HRID1466229

反应详情

EQUATION

反应方程式

HRID 1466229 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

PROCEDURE

实验过程

4-[(2,6-Dichloro-benzoylamino)methyl]phenylboronic acid (5 g, 15.4 mmol), potassium carbonate (5 g), and [1,1′bis(diphenylphosphino)ferrocene]dichloropalladium (II) (0.56 g, 0.77 mmol) were combined in a round bottom flask. 4-Bromo-2-(t-butoxy) pyridine (3.55 g, 15.4 mmol) was dissolved in 20 mL DMF and added to the flask under stirring. The flask was flushed with nitrogen and 10 mL water was added. The reaction mixture was stirred at 70° C. for two hours. After cooling the mixture was poured into 300 mL ethyl acetate and washed with water and brine. The organic phase was dried with magnesium sulfate and evaporated under vacuum. The crude N-[4-(2-tert-butoxy-pyridin-4-yl)-benzyl]-2,6-dichloro-benzamide was further purified by silica gel chromatography (eluent: hexone/ethyl acetate 1:1).

WORKUP

后处理

  1. additionadded to the flask
  2. customThe flask was flushed with nitrogen and 10 mL water
  3. additionwas added
  4. stirringThe reaction mixture was stirred at 70° C. for two hours
  5. temperatureAfter cooling the mixture
  6. additionwas poured into 300 mL ethyl acetate
  7. washwashed with water and brine
  8. dry with materialThe organic phase was dried with magnesium sulfate
  9. customevaporated under vacuum
  10. customThe crude N-[4-(2-tert-butoxy-pyridin-4-yl)-benzyl]-2,6-dichloro-benzamide was further purified by silica gel chromatography (eluent: hexone/ethyl acetate 1:1)