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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 427442Generated: October 30, 2026

p-Bromobenzenesulfonyl chloride → HCID 6734934, compound

https://huagongshe.com/reaction/427442

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Bromobenzenesulfonyl chlorideHCID 7396—
ReactantTriethylamineHCID 8471—
Reactant1-(4-Pyridyl)piperazineHCID 70517—
SolventDichloromethaneHCID 6344—
ProductHCID 6734934HCID 673493473.2%

Reaction Steps

A solution of 1-(4-pyridyl)piperazine (0.49 g) and triethylamine (0.7 ml) in dry dichloromethane (20 ml) was treated slowly with a solution of 4-bromophenylsulphonyl chloride (0.77 g) in dry dichloromethane (10 ml). The reaction mixture was then stirred under argon for 2 hours. The dichloromethane solvent was removed by evaporation and the residue dissolved in ethyl acetate. The organic extracts were washed with water, brine, dried (MgSO4) and evaporated to yield a white crystalline solid which was recrystallised from ethyl acetate to give 1-(4-pyridyl)-4-(4-bromophenylsulphonyl)piperazine (0.84 g) as a solid, m.p. 199-200° C.: microanalysis, found: C, 47.3; H, 4.1; N, 10.9%; C15H16BrN3O2S requires: C, 47.1; H, 4.22; N, 11.0%; NMR: (CDCl3) 3.13(t,4H), 3.42(t,4H), 6.62(dd,2H), 7.67(q,4H), 8.29(d,2H): MS: m/z 382 (MH)−.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06313127B1
Source datasetuspto-grants-2001_11
ORD IDord-d9ce987aa31c44f39775564a23a78877
Source noteuspto-grants-2001_11