反应 #2298652
ord-4a0510c5cc494337a982ce1b30adb051
反应方程式
4-(1H-indazol-3-yl)-1-piperazinecarbonitrile
NaOH
→
desired compound
收率 73.0%
3-(1-Piperazinyl)-1H-indazole
收率 73.0%
溶剂
反应条件
详细条件
See reaction.notes.procedure_details.
后处理
- 1温度at reflux for 4.5 hours
- 2温度The reaction was cooled in an ice bath
- 3萃取The basic solution was extracted with ethyl acetate
- 4洗涤The ethyl acetate was washed with H2O
- 5干燥dried with MgSO4
- 6浓缩concentrated
实验过程
A mixture of 4-(1H-indazol-3-yl)-1-piperazinecarbonitrile (8.0 g, 0.04 mol) and 25% H2SO4 (100 ml) was stirred at reflux for 4.5 hours. The reaction was cooled in an ice bath and made basic by the dropwise addition of 50% NaOH. The basic solution was extracted with ethyl acetate. The ethyl acetate was washed with H2O, dried with MgSO4, and concentrated to afford 5.2 g (73%) of the desired compound, as a solid. The solid was recrystallized twice from toluene to afford 3.0 g of 3-(1-piperazinyl)-1H-indazole, m.p.=153°-155° C.