HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1656988Generated: November 2, 2026
Potassium Carbonate → 2-Amino-4-methyl-5-(2-pyrimidinylthio)thiazole
https://huagongshe.com/reaction/1656988
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 178418793 | HCID 178418793 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-Amino-4-methyl-5-(2-pyrimidinylthio)thiazole | HCID 15729188 | 58% |
Reaction Steps
A mixture of 2-amino-5-bromo-4-methylthiazole hydrochloride (1.15 g), 2-mercaptopyrimidine (0.6 g) and potassium carbonate (1.7 g) in N,N-dimethylformamide (20 ml) was heated at 90° C. for 3.5 hours with stirring. The reaction mixture was poured into ice water. 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: 100 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-amino-4-methyl-5-(2-pyrimidinylthio)thiazole (0.65 g, yield: 58.0%). mp: 165°-170° C. (dec.) IR (Nujol): 3300, 3175, 1630, 1555, 1490, 1320 cm-1
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05256675 |
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| Source dataset | uspto-grants-1993_10 |
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| ORD ID | ord-b7fc3d6e311d4898a112258e82979214 |
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| Source note | uspto-grants-1993_10 |
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