HRID540808

反应详情

EQUATION

反应方程式

HRID 540808 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

CONDITIONS

反应条件

温度
105 °C

PROCEDURE

实验过程

Trimethyl orthobutyrate (29.75 mL, 0.1859 mol) was added in three portions to a solution of 7-benzyloxy-N4-(2-methylpropyl)quinoline-3,4-diamine (54.6 g, 0.170 mol) in toluene (795 mL). Pyridine hydrochloride (1.96 g) was then added, and the reaction was heated at 105° C. and stirred for four hours. Additional trimethyl orthobutyrate (7 mL, 40 mmol) was then added, and the reaction was stirred for three hours. The reaction was allowed to cool to ambient temperature, and the solvent was removed under reduced pressure. The oily residue was treated with chloroform, which was removed under reduced pressure to remove residual toluene, and then again diluted with chloroform (1.2 L). The resulting solution was washed sequentially with 5% aqueous sodium bicarbonate, water, and brine; dried over magnesium sulfate; filtered; and concentrated under reduced pressure to yield 60.3 g of 7-benzyloxy-1-(2-methylpropyl)-2-propyl-1H-imidazo[4,5-c]quinoline as an oily brown solid, containing a small amount of toluene (0.93 equivalents).

WORKUP

后处理

  1. stirringthe reaction was stirred for three hours
  2. temperatureto cool to ambient temperature
  3. customthe solvent was removed under reduced pressure
  4. additionThe oily residue was treated with chloroform, which
  5. customwas removed under reduced pressure
  6. customto remove residual toluene
  7. additionagain diluted with chloroform (1.2 L)
  8. washThe resulting solution was washed sequentially with 5% aqueous sodium bicarbonate, water, and brine
  9. dry with materialdried over magnesium sulfate
  10. filtrationfiltered
  11. concentrationand concentrated under reduced pressure