HRID1773751

反应详情

EQUATION

反应方程式

HRID 1773751 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

CONDITIONS

反应条件

温度
70 °C

PROCEDURE

实验过程

A solution of tert-butyl 6-(3,5-dimethylisoxazol-4-yl)-2-ethoxy-4-formyl-1H-benzo[d]imidazole-1-carboxylate (100 mg, 0.26 mmol), pentafluoroiodoethane (350 mg, 1.42 mmol) and DMF was cooled to −15° C. under nitrogen. Tetra(dimethlamino)ethylene was added (0.33 mL, 1.42 mmol) and the reaction mixture was irradiated with a sun lamp. A thick precipitate formed, and after 30 minutes, the reaction mixture was diluted with ethyl acetate filtered. The filtrate was washed with water and the organic layer was concentrated and dissolved in ethanol (3 mL) and 4M HCl in dioxane (1 mL) and heated to 70° C. for 1 h. The reaction mixture was concentrated and purified by reverse-phase HPLC to give the desired product as a white powder.

WORKUP

后处理

  1. customthe reaction mixture was irradiated with a sun lamp
  2. customA thick precipitate formed
  3. filtrationfiltered
  4. washThe filtrate was washed with water
  5. concentrationthe organic layer was concentrated
  6. dissolutiondissolved in ethanol (3 mL)
  7. concentrationThe reaction mixture was concentrated
  8. custompurified by reverse-phase HPLC