HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 660440Generated: October 29, 2026
Potassium Iodide → HCID 57811380, compound
https://huagongshe.com/reaction/660440
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Propanoic acid, 2-bromo-2-methyl-, ethyl ester | HCID 11745 | — |
| Reactant | HCID 178509206 | HCID 178509206 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 57811380 | HCID 57811380 | 27.3% |
Reaction Steps
Ethyl 2-bromo-2-methylpropanoate (184 μL, 1.239 mmol) was added to a solution of 5-amino-4-(4-cyclopropylnaphthalen-1-yl)-4H-1,2,4-triazole-3-thiol (0.35 g, 1.239 mmol) in DMF (2.5 mL) and heated at 60° C. for 20 hours after which time a few crystals of potassium iodide were added and the mixture heated at 70° C. for a further 24 h. The temperature was then increased to 90° C. and the mixture heated for an additional 6 days. The mixture was allowed to cool to room temperature, concentrated and dissolved in dichloromethane. Triethylamine and water were added and the layers separated. The aqueous layer was extracted with dichloromethane (2×) and the combined organic extracts dried over NaSO4, filtered, concentrated and purified by column chromatography (ethyl acetate) to afford ethyl 2-(5-amino-4-(4-cyclopropylnaphthalen-1-yl)-4H-1,2,4-triazol-3-ylthio)-2-methylpropanoate as a tan solid (0.134 g, 27%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08084483B2 |
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| Source dataset | uspto-grants-2011_12 |
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| ORD ID | ord-31cd91b705234e68a2854cc1a6fc15db |
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| Source note | uspto-grants-2011_12 |
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