HRID1818195

反应详情

EQUATION

反应方程式

HRID 1818195 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

CONDITIONS

反应条件

温度
4 °C

PROCEDURE

实验过程

A solution of tert-butyl 4-[2-(4-amino-7-bromo-2-ethoxymethyl-1H-imidazo[4,5-c]quinolin-1-yl)ethyl]-4-oxidopiperazine-1-carboxylate (8.84 g, 16.1 mmol) in chloroform (400 mL) was cooled to 4° C. Phosphorous trichloride (9.82 mL, 113 mmol) was added dropwise, and the reaction was stirred for 45 minutes at 4° C. Water (one drop) was added to the reaction, which was allowed to warm to ambient temperature. The chloroform was removed under reduced pressure, and the residue was dissolved in ethanol (150 mL). Hydrogen chloride (21.5 mL of a 3 M solution in ethanol) was added, and the reaction was heated at reflux for 25 minutes. The reaction was allowed to cool to room temperature; a precipitate formed and was isolated by filtration to provide 6.86 g of 7-bromo-2-ethoxymethyl-1-(2-piperazin-1-ylethyl)-1H-imidazo[4,5-c]quinolin-4-amine dihydrochloride as a light yellow solid.

WORKUP

后处理

  1. temperatureto warm to ambient temperature
  2. customThe chloroform was removed under reduced pressure
  3. dissolutionthe residue was dissolved in ethanol (150 mL)
  4. additionHydrogen chloride (21.5 mL of a 3 M solution in ethanol) was added
  5. temperaturethe reaction was heated
  6. temperatureat reflux for 25 minutes
  7. temperatureto cool to room temperature
  8. customa precipitate formed
  9. customwas isolated by filtration