HRID489754

反应详情

EQUATION

反应方程式

HRID 489754 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

3

CONDITIONS

反应条件

温度
80 °C

PROCEDURE

实验过程

Under a nitrogen atmosphere, a mixture of 5-isopropoxy-3-bromopyridine (847.0 mg, 3.92 mmol), N-methyl-N-(tert-butoxycarbonyl)-4-penten-2-amine (784.7 mg, 3.94 mmol), palladium(II) acetate (9.0 mg, 0.04 mmol), tri-o-tolylphosphine (50.0 mg, 0.16 mmol), triethylamine (0.73 g, 7.21 mmol), and anhydrous acetonitrile (2 mL) was stirred and heated under reflux at 80° C. for 20 h. The mixture, containing solids was cooled, diluted with water (10 mL), and extracted with CHCl3 (3×10 mL). The combined CHCl3 extracts were dried (Na2SO4), filtered, and concentrated by rotary evaporation to give an oily residue (1.56 g). The crude product was purified by column chromatography on silica gel, eluting with 25-40% (v/v) ethyl acetate in hexane. Selected fractions containing the product were combined and concentrated to give 1.15 g (87.8%) of a light-amber oil.

WORKUP

后处理

  1. temperatureheated
  2. additionThe mixture, containing solids
  3. temperaturewas cooled
  4. extractionextracted with CHCl3 (3×10 mL)
  5. dry with materialThe combined CHCl3 extracts were dried (Na2SO4)
  6. filtrationfiltered
  7. concentrationconcentrated by rotary evaporation