HRID503834

反应详情

EQUATION

反应方程式

HRID 503834 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

CONDITIONS

反应条件

温度
50 °C

PROCEDURE

实验过程

A 200-mL round-bottomed flask equipped with mechanical stirrer was charged with 5-Methyl-4-nitro-1-(pyridin-4-yl)methyl-1H-benzimidazole (881 mg, 3.46 mmol), iron powder (−325 mesh, 3.87 g, 6.92 mmol) and acetic acid (50 mL), and the resulting mixture stirred at 50° C. for 15 min. After this time the reaction was cooled to room temperature, diluted with 1:1 methylene chloride/methanol (1 L) and filtered through a pad of Celite 521. After washing the filter cake with 1:1 methylene chloride/methanol (2×50 mL), the filtrate was concentrated in vacuo. The resulting residue was dissolved in methylene chloride (50 mL) and vigorously stirred with 1M aqueous sodium hydroxide (50 mL). The resulting emulsion was filtered through a pad of Celite 521, the pad washed with methylene chloride (2×25 mL) and the organic layer of the filtrate separated and dried over sodium sulfate. Removal of the drying agent by filtration, followed by evaporation of the filtrate in vacuo gave a residue which was purified by flash chromatography. This purified material was dissolved in warm methylene chloride (15 mL) and the solution diluted with hexanes (35 mL). The resulting precipitate was filtered, washed with hexanes (3×100 mL) and dried under reduced pressure for 1.5 h to afford compound 2d as an off-white solid.

WORKUP

后处理

  1. customA 200-mL round-bottomed flask equipped with mechanical stirrer
  2. temperatureAfter this time the reaction was cooled to room temperature
  3. filtrationfiltered through a pad of Celite 521
  4. washAfter washing the filter cake with 1:1 methylene chloride/methanol (2×50 mL)
  5. concentrationthe filtrate was concentrated in vacuo
  6. dissolutionThe resulting residue was dissolved in methylene chloride (50 mL)
  7. stirringvigorously stirred with 1M aqueous sodium hydroxide (50 mL)
  8. filtrationThe resulting emulsion was filtered through a pad of Celite 521
  9. washthe pad washed with methylene chloride (2×25 mL)
  10. customthe organic layer of the filtrate separated
  11. dry with materialdried over sodium sulfate
  12. customRemoval of the drying agent
  13. filtrationby filtration
  14. customfollowed by evaporation of the filtrate in vacuo
  15. customgave a residue which
  16. customwas purified by flash chromatography
  17. dissolutionThis purified material was dissolved in warm methylene chloride (15 mL)
  18. additionthe solution diluted with hexanes (35 mL)
  19. filtrationThe resulting precipitate was filtered
  20. washwashed with hexanes (3×100 mL)
  21. customdried under reduced pressure for 1.5 h