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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1657002Generated: October 31, 2026

m-Chloroperbenzoic acid → 2-Amino-5-(5-trifluoromethylpyridin-2-ylsulfinyl)thiazole

https://huagongshe.com/reaction/1657002

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
Reactant2-Amino-5-(5-trifluoromethylpyridin-2-ylthio)thiazoleHCID 15729200—
SolventDichloromethaneHCID 6344—
Product2-Amino-5-(5-trifluoromethylpyridin-2-ylsulfinyl)thiazoleHCID 1572920581.9%

Reaction Steps

To a solution of 2-amino-5-(5-trifluoromethylpyridin-2-ylthio)thiazole (0.6 g) in dichloromethane (20 ml) was added portionwise 3-chloroperbenzoic acid (0.6 g) at 5° C. with stirring. The mixture was stirred at 5° C. for 3 hours. The reaction mixture was washed with aqueous sodium bicarbonate and dried over magnesium sulfate. The solvent was concentrated under reduced pressure to give solid. The solid was subjected to column chromatography on silica gel (silica gel 60, 70-230 mesh; Merck: 30 g) and eluted with a mixture of chloroform and methanol (10:1). The fractions containing the objective compound were combined and concentrated under reduced pressure to give 2-amino-5-(5-trifluoromethylpyridin-2-ylsulfinyl)thiazole (0.52 g, yield: 81.9%). mp: 144°-145° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05256675
Source datasetuspto-grants-1993_10
ORD IDord-faaa2f8cb7da41e4a467e7ae572ff0cb
Source noteuspto-grants-1993_10