HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2380628Generated: October 29, 2026
Potassium Carbonate → 2-Amino-4-methyl-5-(2-pyridylthio)thiazole
https://huagongshe.com/reaction/2380628
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Amino-5-bromo-4-methyl-1,3-thiazole hydrochloride | HCID 18954728 | — |
| Reactant | HCID 178418616 | HCID 178418616 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-Amino-4-methyl-5-(2-pyridylthio)thiazole | HCID 18954735 | 48% |
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
| 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-d50d9767591e4e9ebe7d18131b2ca2c2 |
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| Source note | uspto-grants-1994_11 |
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