HRID265332

反应详情

EQUATION

反应方程式

HRID 265332 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

1-(2,4-Difluorophenyl)-1-(4-(4-carbamoylthiazol-2-yl)-thiophen-2-yl)-2-(1H-1,2,4-triazol-1-yl)ethanol (1.2 g) was dissolved in pyridine (7.1 ml). The solution was cooled on an ice bath, and phosphorus oxychloride (0.29 ml) was added thereto. The resultant mixture was stirred for 30 minutes. After the reaction, the reaction mixture was added with saline and extracted with ethyl acetate. An organic layer was washed once with 6N hydrochloric acid (20 ml) and then each once with water, a saturated aqueous solution of sodium hydrogencarbonate and saturated saline. After the thus-washed organic layer was dried over magnesium sulfate, the solvent was distilled out, and the residue was purified by chromatography on silica gel. Recrystallization from a solution of dichloromethane in ether was further conducted to obtain a solid (800 mg). Melting point: 172°-173° C.

WORKUP

后处理

  1. temperatureThe solution was cooled on an ice bath
  2. customAfter the reaction
  3. additionthe reaction mixture was added with saline
  4. extractionextracted with ethyl acetate
  5. washAn organic layer was washed once with 6N hydrochloric acid (20 ml)
  6. dry with materialAfter the thus-washed organic layer was dried over magnesium sulfate
  7. distillationthe solvent was distilled out
  8. customthe residue was purified by chromatography on silica gel
  9. customRecrystallization from a solution of dichloromethane in ether