HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1875873Generated: October 25, 2026
2-Aminothiazole → N-(thiazol-2-yl)-1H-imidazole-1-carbothioamide
https://huagongshe.com/reaction/1875873
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Aminothiazole | HCID 2155 | — |
| Reactant | 1,1'-Thiocarbonyldiimidazole | HCID 80264 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-(thiazol-2-yl)-1H-imidazole-1-carbothioamide | HCID 10750950 | 83.1% |
Reaction Steps
To thiazol-2-amine (2.12 g, 21.17 mmol) in acetonitrile (30 mL) and tetrahydrofuran (5 mL) was added di(1H-imidazol-1-yl)methanethione (4.90 g, 27.5 mmol). The reaction was stirred at 60° C. for 5 hours. The reaction was cooled to room temperature and the precipitate was filtered and washed with cold acetonitrile (2×15 mL) to afford an orange-brown powder. The product, N-(thiazol-2-yl)-1H-imidazole-1-carbothioamide (3.70 g, 17.60 mmol, 83% yield), was taken directly to the next step without any further characterization.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08309577B2 |
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| Source dataset | uspto-grants-2012_11 |
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| ORD ID | ord-aaddb676184541509234f6b1acb5d3a0 |
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| Source note | uspto-grants-2012_11 |
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