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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 130430Generated: October 25, 2026

5-Bromothiophene-2-sulfonyl chloride → 5-Bromo-N-{5-(cis-3,5-dimethyl-1-piperazinyl)-2-[(phenylmethyl)oxy]phenyl]-2-thiophenesulfonamide

https://huagongshe.com/reaction/130430

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Bromothiophene-2-sulfonyl chlorideHCID 2733924—
Reactant5-(cis-3,5-Dimethyl-1-piperazinyl)-2-[(phenylmethyl)oxy]anilineHCID 59007092—
SolventPyridineHCID 1049—
SolventDichloromethaneHCID 6344—
Product5-Bromo-N-{5-(cis-3,5-dimethyl-1-piperazinyl)-2-[(phenylmethyl)oxy]phenyl]-2-thiophenesulfonamideHCID 59007096—

Reaction Steps

A solution of 5-(cis-3,5-dimethyl-1-piperazinyl)-2-[(phenylmethyl)oxy]aniline (D39) (300 mg, 0.96 mmol) in dichloromethane (5 ml) and pyridine (5 ml) was added 5-bromo-2-thiophenesulfonyl chloride (505 mg, 1.93 mmol) and the mixture stirred at room temperature for 4 hours. The mixture was then reduced in vacuo and the residue purified by SCX (eluting with methanol then ammonia 2M in methanol). The appropriate fractions were combined and reduced and the residue purified by trituaration with methanol to afford the title compound (D42). MS (ES+) m/e 536/538 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07381728B2
Source datasetuspto-grants-2008_06
ORD IDord-4ecedd6316164cc78f6a55d979f81622
Source noteuspto-grants-2008_06