24188-78-1

物理化学性质
制备方法

77077-83-9

24188-78-1
步骤2:将4-甲基-2H-异喹啉-1-酮(4.8 g)溶于三氯氧磷(50 mL)中,加热回流3小时。反应完成后,冷却至室温并减压浓缩。残余物用5 N氢氧化钠水溶液处理,随后用二氯甲烷萃取。合并有机层,用饱和食盐水洗涤,无水硫酸镁干燥。过滤后,滤液减压浓缩,所得粗产物通过Biotage快速色谱法纯化,洗脱剂为5%乙酸乙酯的己烷溶液,得到4.8 g(收率90%)目标产物1-氯-4-甲基异喹啉,为白色固体。产物结构经1H NMR(400 MHz,CDCl3)确认:δ 2.59(s,3H),7.68(t,J = 7.70 Hz,1H),7.78(m,1H),7.94(d,J = 8.31 Hz,1H),8.11(s,1H),8.35(d,J = 8.31 Hz,1H)。
参考文献:
[1] Patent: US2006/183694, 2006, A1. Location in patent: Page/Page column 73-74
[2] Patent: WO2003/99274, 2003, A1. Location in patent: Page 324-325
[3] Patent: US2007/99825, 2007, A1. Location in patent: Page/Page column 62
[4] Patent: US2008/107623, 2008, A1. Location in patent: Page/Page column 57
[5] Patent: US2008/107624, 2008, A1. Location in patent: Page/Page column 60