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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1982278Generated: November 2, 2026

4-Bromoaniline → N-(4-Bromophenyl)-4-[(propane-2-sulfonyl)amino]benzamide

https://huagongshe.com/reaction/1982278

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-BromoanilineHCID 7807—
ReactantTriethylamineHCID 8471—
ReactantSodium BicarbonateHCID 516892—
Reactant4-[(Propane-2-sulfonyl)amino]benzoyl chlorideHCID 13489981—
SolventDichloromethaneHCID 6344—
ProductN-(4-Bromophenyl)-4-[(propane-2-sulfonyl)amino]benzamideHCID 1348998252.7%

Reaction Steps

A mixture of 250 mg of 4-isopropanesulfonamidobenzoylchloride 1, 181 mg of 4-bromoaniline 2, 106 mg of triethylamine, and 5 ml of methylene chloride is stirred at room temperature for 5 minutes. The reaction mixture is neutralized with a sodium bicarbonate solution, and extracted with methylene chloride. The organic layer is concentrated under reduced pressure, and the residue is chromatographed on a column of silica-gel. The eluate with 3% methanolmethylene chloride is concentrated, and the residue is crystallized from ethyl acetate-isopropyl ether. The crude resulting crystals are recrystallized from ethyl acetateisopropyl ether to give 200 mg of 4'-bromo-4-isopropanesulfonamidobenzanilide 3 as pure specimen, m.p. 213°-214° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04595780
Source datasetuspto-grants-1986_06
ORD IDord-b2d4a1026a424abfac07f803ca26f855
Source noteuspto-grants-1986_06