HRID1898817

反应详情

EQUATION

反应方程式

HRID 1898817 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

PROCEDURE

实验过程

A mixture of 9.9 g (0.10 mol) of copper (I) chloride with 300 mL of acetonitrile was prepared and 8.7 mL (6.8 g, 0.066 mol) of 90 percent t-butyl nitrite was added with stirring. After 10 minutes 9.5 g (0.033 mol) of 8-amino-2-benzylthio-5-chloro[1,2,4]triazolo[1,5-a]pyridine was added and the reaction mixture was allowed to react with stirring for 3 days. The mixture was then diluted with dichloromethane and 2N aqueous hydrochloric acid, and after mixing this well, the phases were separated. The organic layer was washed with 2N aqueous hydrochloric acid and concentrated by evaporation under reduced pressure. The residue was chromatographed on silica gel eluting with dichloromethane to obtain 6.5 g (63 percent of theory) of the title compound as a yellow powder melting at 103°-104° C.

WORKUP

后处理

  1. customwas prepared
  2. customto react
  3. stirringwith stirring for 3 days
  4. additionafter mixing this well, the phases
  5. customwere separated
  6. washThe organic layer was washed with 2N aqueous hydrochloric acid
  7. concentrationconcentrated by evaporation under reduced pressure
  8. customThe residue was chromatographed on silica gel eluting with dichloromethane