反应 #2298651

ord-bb8a164b80884f129ec2b101bfba4921

反应方程式

O
H2O
CN1CCN(c2nn(S(=O)(=O)c3ccccc3)c3ccccc23)CC1
3-(4-methyl-1-piperazinyl)-1-phenylsulfonyl-1H-indazole
O=C([O-])[O-].[K+].[K+]
K2CO3
N#CBr
cyanogen bromide
N#CN1CCN(c2nn(S(=O)(=O)c3ccccc3)c3ccccc23)CC1
4-[1-(Phenylsulfonyl)-1H-indazol-3-yl]-1-piperazinecarbonitrile

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    其他The solid, which precipitated from solution
  2. 2
    过滤was collected by filtration
  3. 3
    洗涤was washed well with H2O affording 168 g (68%) of product
  4. 4
    其他A 5.2 g sample was recrystallized twice from ethanol-H2O yielding 4.0 g of 4-[1-(phenylsulfonyl)-1H-indazol-3-yl]-1-piperazinecarbonitrile, m.p.=178°-180° C.

实验过程

To a stirred mixture of 3-(4-methyl-1-piperazinyl)-1-phenylsulfonyl-1H-indazole (237 g, 0.67 mol), K2CO3 (102 g, 0.74 mol) and dimethylsulfoxide (DMSO, 2000 ml), under nitrogen, was added cyanogen bromide (72 g, 0.68 mol) dissolved in DMSO (525 ml). The reaction was stirred at ambient temperature for 5.5 hours and was then poured into H2O (7 l). The solid, which precipitated from solution, was collected by filtration and was washed well with H2O affording 168 g (68%) of product. A 5.2 g sample was recrystallized twice from ethanol-H2O yielding 4.0 g of 4-[1-(phenylsulfonyl)-1H-indazol-3-yl]-1-piperazinecarbonitrile, m.p.=178°-180° C.

来源

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