反应 #452485
ord-0debfc1f785f4189a107bae53f0f3f30
反应方程式
反应条件
后处理
- 1温度After the resulting mixture was heated
- 2温度under reflux
- 3workup.DISTILLATIONthe solvent was distilled off
- 4workup.DISSOLUTIONThe residue was dissolved in acetone (50 ml)
- 5workup.STIRRINGThe thus-obtained mixture was stirred for 1 hour
- 6其他A deposited precipitate was removed
- 7workup.DISTILLATIONthe solvent was distilled off
- 8workup.DISSOLUTIONThe residue was dissolved in ethyl ether
- 9洗涤The resulting solution was washed with an aqueous solution of sodium chloride
- 10干燥dried over anhydrous magnesium sulfate
- 11workup.DISTILLATIONThe solvent was distilled off
- 12workup.DISSOLUTIONthe residue was dissolved in methanol
- 13workup.ADDITIONfollowed by the addition of concentrated hydrochloric acid (5 ml) for acidification
- 14workup.DISTILLATIONThe solvent was distilled off
- 15其他the thus-obtained residue was crystallized from a mixed solvent of ethanol and methanol
实验过程
Thionyl chloride (6 ml) was added to a suspension of quinaldinic acid (3.463 g, 20 mmol) in chloroform (40 ml). After the resulting mixture was heated under reflux and stirring for 6 hours, the solvent was distilled off. The residue was dissolved in acetone (50 ml), followed by the addition of a solution of N-benzylpiperazine (10.576 g, 60 mmol) in acetone (50 ml). The thus-obtained mixture was stirred for 1 hour. A deposited precipitate was removed, and the solvent was distilled off. The residue was dissolved in ethyl ether. The resulting solution was washed with an aqueous solution of sodium chloride, and then dried over anhydrous magnesium sulfate. The solvent was distilled off, and the residue was dissolved in methanol, followed by the addition of concentrated hydrochloric acid (5 ml) for acidification. The solvent was distilled off and the thus-obtained residue was crystallized from a mixed solvent of ethanol and methanol, whereby 7.166 g of the title compound were obtained as white powder (yield: 97.5%).