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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2184485Generated: October 29, 2026

Water → 4-[1-(Phenylsulfonyl)-1H-indazol-3-yl]-1-piperazinecarbonitrile

https://huagongshe.com/reaction/2184485

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantCyanogen BromideHCID 10476—
ReactantPotassium CarbonateHCID 11430—
Reactant1-(Benzenesulfonyl)-3-(4-methylpiperazin-1-yl)-1H-indazoleHCID 14823425—
SolventDimethyl SulfoxideHCID 679—
Product4-[1-(Phenylsulfonyl)-1H-indazol-3-yl]-1-piperazinecarbonitrileHCID 14823443—

Reaction Steps

To a stirred mixture of 3-(4- methyl-1-piperazinyl)-1-phenylsulfonyl-1H-indazole (237 g, 0.67 mole), K2CO3 (102 g, 0.74 mole) and dimethylsulfoxide (DMSO, 2000 ml), under nitrogen, was added cyanogen bromide (72 g, 0.68 mmol) 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 with ethanol-H2O yielding 4.0 g of 4-[1-(phenylsulfonyl)-1H-indazol-3-yl]-1-piperazinecarbonitrile, m.p.=178°-180° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUSRE037729E1
Source datasetuspto-grants-2002_06
ORD IDord-de235bb7c166476796d30a6a66578cc1
Source noteuspto-grants-2002_06