HRID231547

反应详情

EQUATION

反应方程式

HRID 231547 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

A solution of 7-(3-aminopropoxy)-2-methyl-1,2,3,4-tetrahydroisoquinoline (5.43 g) in methanol (70 ml) is slowly added over a period of 45 minutes to a stirred solution of 3,4-dimethoxy-1,2,5-thiadiazole-1-oxide (3.68 g) in 375 ml of methanol at a temperature of 3° C. The reaction mixture is stirred for an additional one hour and 25.0 g anhydrous ammonia is bubbled in over a period of 10 minutes. The resulting mixture is warmed to RT with stirring and the solution is evaporated in vacuo. The near-white solid residue is dissolved in hot 95% ethanol, filtered hot and rinsed with hot ethanol. The solution is cooled with stirring, then stirred in an ice bath for 30 minutes and filtered. The resulting solid is washed with cold ethanol and diethyl ether and dried in air, giving the desired tetrahydroisoquinoline thiadiazole-1-oxide as a white powder, M.P. 193°-194° C.

WORKUP

后处理

  1. custom25.0 g anhydrous ammonia is bubbled in over a period of 10 minutes
  2. stirringwith stirring
  3. customthe solution is evaporated in vacuo
  4. dissolutionThe near-white solid residue is dissolved in hot 95% ethanol
  5. filtrationfiltered hot
  6. washrinsed with hot ethanol
  7. temperatureThe solution is cooled
  8. stirringwith stirring
  9. stirringstirred in an ice bath for 30 minutes
  10. filtrationfiltered
  11. washThe resulting solid is washed with cold ethanol and diethyl ether
  12. customdried in air