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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1434679Generated: October 26, 2026

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

https://huagongshe.com/reaction/1434679

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 numberUS07615569B2
Source datasetuspto-grants-2009_11
ORD IDord-b0ab6d0f2a8943d5ac9a9aa56c844e59
Source noteuspto-grants-2009_11