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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1656983Generated: October 31, 2026

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

https://huagongshe.com/reaction/1656983

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 acetate (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-1,3,4-thiadiazol-5-ylthio)thiazole (1.65 g, yield: 60.7%). mp: 242°-244° C. IR (Nujol): 3250, 1695, 1550, 1300 cm-1

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05256675
Source datasetuspto-grants-1993_10
ORD IDord-33375a0fb4514007ba34e570f50669df
Source noteuspto-grants-1993_10