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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2380623Generated: November 2, 2026

Potassium Carbonate → 2-Acetylamino-5-(2-methyl-1,3,4-thiadiazol-5-ylthio)thiazole

https://huagongshe.com/reaction/2380623

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant2-Acetamido-5-chlorothiazoleHCID 4684134—
ReactantHCID 178434161HCID 178434161—
SolventDimethylformamideHCID 6228—
Product2-Acetylamino-5-(2-methyl-1,3,4-thiadiazol-5-ylthio)thiazoleHCID 1572918361.6%

Reaction Conditions

Temperature120 °C

Reaction Steps

A mixture of 2-acetylamino-5-chlorothiazole (1.76 g), 5-mercapto-2-methyl-1,3,4-thiadiazole (1.3 g) and potassium carbonate (2.0 g) in N,N-dimethylformamide (40 ml) was heated at 120° C. for 4 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 titrate (1:1), 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: 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-acetylamino-5-(2-methyl-l,3,4-thiadiazol-5-ylthio)thiazole (1.65 g, yield: 60.7%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05369107
Source datasetuspto-grants-1994_11
ORD IDord-aa61015ae5744d02b221b8966f14e1ad
Source noteuspto-grants-1994_11