反应 #2298652

ord-4a0510c5cc494337a982ce1b30adb051

反应方程式

N#CN1CCN(c2n[nH]c3ccccc23)CC1
4-(1H-indazol-3-yl)-1-piperazinecarbonitrile
[Na+].[OH-]
NaOH
c1ccc2c(N3CCNCC3)n[nH]c2c1
desired compound
收率 73.0%
c1ccc2c(N3CCNCC3)n[nH]c2c1
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. 1
    温度at reflux for 4.5 hours
  2. 2
    温度The reaction was cooled in an ice bath
  3. 3
    萃取The basic solution was extracted with ethyl acetate
  4. 4
    洗涤The ethyl acetate was washed with H2O
  5. 5
    干燥dried with MgSO4
  6. 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.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: USRE039265E1uspto-grants-2006_09