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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1657001Generated: November 4, 2026

Hydrochloric Acid → 2-Amino-5-(5-trifluoromethylpyridin-2-ylthio)thiazole

https://huagongshe.com/reaction/1657001

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTetrahydrofuranHCID 8028—
ReactantHCID 15729199HCID 15729199—
SolventEthanolHCID 702—
Product2-Amino-5-(5-trifluoromethylpyridin-2-ylthio)thiazoleHCID 1572920075.8%

Reaction Steps

A mixture of 2-acetylamino-5-(5-trifluoromethylpyridin-2-ylthio)thiazole (3.2 g) in a mixture of ethanol (60 ml), tetrahydrofuran (30 ml) and aqueous 6N-hydrochloric acid (10 ml) was refluxed for 3 hours with stirring. The reaction mixture was concentrated under reduced pressure and the residue was dissolved in water. The solution was adjusted to pH 8.5 using aqueous sodium bicarbonate and extracted with mixture of tetrahydrofuran and ethyl acetate (1:1) 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: 150 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-ylthio)thiazole (2.1 g, yield: 75.8%). mp: 135°-138° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05256675
Source datasetuspto-grants-1993_10
ORD IDord-a1a5db51116744fc969e6708d504580b
Source noteuspto-grants-1993_10