Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 130441Generated: October 25, 2026

p-Bromobenzenesulfonyl chloride → 4-Bromo-N-[5-(cis-3,5-dimethyl-1-piperazinyl)-2-(methyloxy)phenyl]benzenesulfonamide

https://huagongshe.com/reaction/130441

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Bromobenzenesulfonyl chlorideHCID 7396—
Reactant4-MethylmorpholineHCID 7972—
Reactant5-(cis-3,5-Dimethyl-1-piperazinyl)-2-(methyloxy)anilineHCID 59007063—
SolventDichloromethaneHCID 6344—
Product4-Bromo-N-[5-(cis-3,5-dimethyl-1-piperazinyl)-2-(methyloxy)phenyl]benzenesulfonamideHCID 44452776—

Reaction Steps

A solution of 5-(cis-3,5-dimethyl-1-piperazinyl)-2-(methyloxy)aniline (D4) (1.20 g, 5.1 mmol) in dichloromethane (35 ml) was treated with morpholinomethyl-polystyrene HL resin (2.45 g, 4.2 mmol/g loading, 10.29 mmol) followed by 4-bromobenzenesulfonyl chloride (2.60 g, 10.2 mmol). The resulting solution was stirred at room temperature overnight (˜24hours)and then the resin filtered off with methanol and the solvent evaporated in vacuo. The residue was passed through an SCX column eluting first with methanol followed by 2M ammonia in methanol. The relevant fractions were collected, combined and the solvent evaporated in vacuo. The crude product was purified by Flashmaster causing an elution gradient of 0 to 10% methanol in dichloromethane. The relevant fractions were collected, combined and the solvent evaporated to afford the title compound (E106). MS (ES+) m/e 454/456 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07381728B2
Source datasetuspto-grants-2008_06
ORD IDord-5f4f9e09ca37412db2a3eae206990843
Source noteuspto-grants-2008_06