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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 559501Generated: October 30, 2026

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

https://huagongshe.com/reaction/559501

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 numberUS08063080B2
Source datasetuspto-grants-2011_11
ORD IDord-130978aa94e344abb751a468a34eae30
Source noteuspto-grants-2011_11