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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Acetamido-5-chlorothiazole | HCID 4684134 | — |
| Reactant | HCID 178434161 | HCID 178434161 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-Acetylamino-5-(2-methyl-1,3,4-thiadiazol-5-ylthio)thiazole | HCID 15729183 | 61.6% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05369107 |
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| Source dataset | uspto-grants-1994_11 |
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| ORD ID | ord-aa61015ae5744d02b221b8966f14e1ad |
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| Source note | uspto-grants-1994_11 |
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