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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 225430Generated: October 27, 2026

Benzenesulfonyl chloride → HCID 22174837, compound

https://huagongshe.com/reaction/225430

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzenesulfonyl chlorideHCID 7369—
ReactantSodium hydrideHCID 24758—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 22174830HCID 22174830—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 22174837HCID 2217483791%

Reaction Steps

A solution of 4-(4-benzylpiperazin-1-yl)-1H-indazole (2.34 g, 8.00 mmol) in dry dimethyl formamide is treated with 0.48 g unwashed 60% NaH in mineral oil (12.0 mmol of NaH). After stirring under nitrogen for 15 min, the reaction is treated with benzenesulfonylchloride (1.53 mL, 12.0 mmol), stirred for 24 hr at ambient temperature, treated with saturated aqueous NaHCO3 and water and extracted with ether. The organic layer is washed sequentially with water and brine, dried over MgSO4 and concentrated in vacuo to give a residue. The residue is purified by flash chromatography on silica gel using 1:1 ethyl acetate:hexanes as eluant to afford the free amine of the title compound as an oil (3.14 g, 91%). A portion of this oil (432 mg, 1.0 mmol) is dissolved in ether and treated with 1.0M HCl in ether (1.1 mL, 1.1 mmol). The resulting solid is filtered, washed with ether, and dried under vacuum to provide the title compound as a light tan solid, mp 208-209° C., identified by HNMR and mass spectral analyses.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07557098B2
Source datasetuspto-grants-2009_07
ORD IDord-7cd37b52b51040e286cd55bb2d4c3390
Source noteuspto-grants-2009_07