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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1656989Generated: October 30, 2026

Potassium Carbonate → 2-Amino-4-methyl-5-(2-pyridylthio)thiazole

https://huagongshe.com/reaction/1656989

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant2-Amino-5-bromo-4-methyl-1,3-thiazole hydrochlorideHCID 18954728—
ReactantHCID 178418616HCID 178418616—
SolventDimethylformamideHCID 6228—
Product2-Amino-4-methyl-5-(2-pyridylthio)thiazoleHCID 1895473548%

Reaction Conditions

Temperature90 °C

Reaction Steps

A mixture of 2-amino-5-bromo-4-methylthiazole hydrochloride (4.5 g), 2-mercaptopyridine (2.3 g) and potassium carbonate (7.0 g) in N,N-dimethylformamide (100 ml) was heated at 90° C. for 3 hours with stirring. The reaction mixture was concentrated under reduced pressure and water was added to this residue. The mixture was extracted with a mixture of tetrahydrofuran and ethyl acetate, washed with aqueous saturated sodium chloride 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: 300 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 oil. Again the oil was subjected to column chromatography on silica gel (silica gel 60, 70-230 mesh; Merck: 200 g) and eluted with a mixture of dichloromethane and acetone (5:1). The fractions containing the objective compound were combined and concentrated under reduced pressure to give 2-amino-4-methyl-5-(2-pyridylthio)thiazole (2.1 g, yield: 47.9%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05256675
Source datasetuspto-grants-1993_10
ORD IDord-44fe6396a3d6416fb4769b7ad40d08ac
Source noteuspto-grants-1993_10