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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1434681Generated: November 2, 2026

2-Aminothiazole → 4-Acetyl-n-(thiazol-2-yl)benzenesulfonamide

https://huagongshe.com/reaction/1434681

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-AminothiazoleHCID 2155—
Reactant4-Acetylbenzenesulfonyl chlorideHCID 266418—
SolventPyridineHCID 1049—
SolventDichloromethaneHCID 6344—
Product4-Acetyl-n-(thiazol-2-yl)benzenesulfonamideHCID 2108252970%

Reaction Steps

A solution of 4-acetyl-benzenesulfonyl chloride (50 mmol) and 2-aminothiazole (50 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-acetyl-N-thiazol-2-yl-benzenesulfonamide (35 mmol) as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07615569B2
Source datasetuspto-grants-2009_11
ORD IDord-c6d290bbaf614ea19e21631e3c9af60c
Source noteuspto-grants-2009_11