HRID269079

反应详情

EQUATION

反应方程式

HRID 269079 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

3

CONDITIONS

反应条件

温度
90 °C

PROCEDURE

实验过程

A mixture of commercially available 2-amino-5-bromopyridine (50.0 g, 289 mmol), trimethylsilylacetylene (112 mL, 809 mmol), Et3N (120 mL, 867 mmol), PdCl2(PPh3)2 (4.06 g, 2 mol %) and PPh3 (1.52 g, 2 mol %) in DMF (290 mL) was purged for 10 min with argon. Then CuI (340 mg, 1 mol %) was added and the reaction mixture was heated up to 90° C., stirring was continued at 90° C. for 4.5 h. Cooled to 23° C., the reaction mixture was concentrated in vacuum to remove all volatiles, poured the residue onto water (300 mL) and extracted with ethyl acetate (3×500 mL). The combined organic layers were washed with water (300 mL) and brine (2×250 mL), dried over MgSO4. Removal of the solvent in vacuum left a dark brown residue which was purified by flash chromatography with n-heptane and acetone to give the title compound as a brown solid (41.65 g, 76%). MS (ISP) 191 [(M+H)+].

WORKUP

后处理

  1. customwas purged for 10 min with argon
  2. additionThen CuI (340 mg, 1 mol %) was added
  3. temperatureCooled to 23° C.
  4. concentrationthe reaction mixture was concentrated in vacuum
  5. customto remove all volatiles
  6. additionpoured the residue onto water (300 mL)
  7. extractionextracted with ethyl acetate (3×500 mL)
  8. washThe combined organic layers were washed with water (300 mL) and brine (2×250 mL)
  9. dry with materialdried over MgSO4
  10. customRemoval of the solvent in vacuum
  11. waitleft a dark brown residue which
  12. customwas purified by flash chromatography with n-heptane and acetone