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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 6975Generated: October 25, 2026

p-Toluenesulfonic acid → N-[4-bromo-2-chlorobenzoyl]-5-bromothiophene-2-sulfonamide

https://huagongshe.com/reaction/6975

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acidHCID 6101—
Reactant4-Bromo-2-chlorobenzoic acidHCID 108829—
Reactant5-Bromo-2-thiophenesulfonamideHCID 1241304—
SolventDichloromethaneHCID 6344—
ProductN-[4-bromo-2-chlorobenzoyl]-5-bromothiophene-2-sulfonamideHCID 22019517—

Reaction Steps

An 8 mL reaction vial is charged with 4-bromo-2-chlorobenzoic acid (0.39 mmol, 1.5 eq) and 2.0 mL of dichloromethane. A stock solution (4.0 mL) containing 5-bromothiophene-2-sulfonamide (0.26 mmol, 1 eq) and N,N-[dimethyl]-4-aminopyridine (48 mg, 0.39 mmol, 1.5 eq) in dichloromethane is added, followed by 0.261 g carbodiimide polystyrene resin (2.0 mmol/g, 0.52 mmol, 2.0 eq, Novabiochem) and the vial is capped and shaken. After 72 hr, 0.77 g sulphonated polystyrene resin (MP-TsOH) is added (1.53 mmol/g, 1.17 mmol, Argonaut). After about 18 hr the reaction mixture is filtered and concentrated under reduced pressure. Chromatography was applied to the residue and fractions containing product were combined and concentrated under reduce pressure to provide the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07084170B2
Source datasetuspto-grants-2006_08
ORD IDord-084376ff6cbd402bbcddd99c0de3c3d7
Source noteuspto-grants-2006_08