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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1840602Generated: November 3, 2026

3-(Bromomethyl)benzene-1-sulfonyl chloride → HCID 23447331, compound

https://huagongshe.com/reaction/1840602

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(Bromomethyl)benzene-1-sulfonyl chlorideHCID 23447389—
ReactantHCID 23447422HCID 23447422—
ProductHCID 23447331HCID 23447331—

Reaction Steps

A solution of 4-[3-(bromomethyl)benzenesulfonyl]-1-(4-cyanobenzyl)-2-piperazinone (1.21 g) obtained from 1-(4-cyanobenzyl)-2-piperazinone hydrochloride and 3-(bromomethyl)benzenesulfonyl chloride according to a method described in Reference Example 6 and imidazole (613 mg) in DMF (20 ml) was stirred at room temperature overnight. The reaction solution was concentrated under reduced pressure, and to the residue was added ethyl acetate. The mixture was washed with sodium bicarbonate solution and saturated brine, dried (MgSO4) and concentrated, and the residue was purified with silica gel column chromatography (ethyl acetate: methanol containing 10% ammonia solution=85: 15) to give pale yellow amorphous of 1-(4-cyanobenzyl)-4-[3-(1H-imidazol-1-ylmethyl)benzenesulfonyl]-2-piperazinone (734 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06680312B2
Source datasetuspto-grants-2004_01
ORD IDord-ba86d92651f0441ca23e321ca63872e7
Source noteuspto-grants-2004_01