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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 559499Generated: October 26, 2026

2-Aminothiazole → 4-bromo-N-(1,3-thiazol-2-yl)benzene-1-sulfonamide

https://huagongshe.com/reaction/559499

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-AminothiazoleHCID 2155—
Reactantp-Bromobenzenesulfonyl chlorideHCID 7396—
SolventPyridineHCID 1049—
SolventDichloromethaneHCID 6344—
Product4-bromo-N-(1,3-thiazol-2-yl)benzene-1-sulfonamideHCID 66930485%

Reaction Steps

A solution of 4-bromo-benzenesulfonyl chloride (100 mmol) and 2-aminothiazole (100 mmol) in dichloromethane and pyridine (300 mL, 8:2) was stirred for one day. After concentrated in vacuo, the residue was diluted with ethyl acetate (500 mL) and the solution was washed with 1N HCl solution, sat NaHCO3, dried over MgSO4, and concentrated in vacuo. The residue was recrystallized in ethyl acetate to give 4-bromo-N-thiazol-2-yl-benzenesulfonamide (85 mmol) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08063080B2
Source datasetuspto-grants-2011_11
ORD IDord-cb89c4a71c3349dea7583ac879f71fac
Source noteuspto-grants-2011_11