HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 891858Generated: October 27, 2026
Ethanol → 3-Trifluoromethyl-imidazo[1,2-B][1,2,4]triazine
https://huagongshe.com/reaction/891858
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethanol | HCID 702 | — |
| Reactant | Ethane, 2-bromo-1,1-diethoxy- | HCID 74852 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 5-(Trifluoromethyl)-1,2,4-triazin-3-amine | HCID 11542832 | — |
| Solvent | Hydrogen Bromide | HCID 260 | — |
| Solvent | Water | HCID 962 | — |
| Product | 3-Trifluoromethyl-imidazo[1,2-B][1,2,4]triazine | HCID 11622469 | 22.5% |
Reaction Steps
A stirred mixture of bromoacetaldehyde diethyl acetal (2.30 ml, 14.8 mmol) in concentrated hydrobromic acid (0.73 ml) and water (0.73 ml) was heated at reflux for 2 h, then poured into ethanol (25 ml). The solution was neutralised to pH 7 with solid sodium hydrogencarbonate, then filtered. To the filtrate was added 3-amino-5-trifluoromethyl-1,2,4-triazine (1.0079 g, 6.14 mmol) and the mixture was stirred at 60° C. for 20 h, then 80° C. for 23 h. The mixture was evaporated in vacuo, and the residue was purified by flash chromatography (silica gel, 35-50% EtOAc/isohexane) to give 0.2593 g (22%) of the title compound: 1H NMR (360 MHz, CDCl3) δ 8.20 (1H, d, J0.8), 8.30 (1H, d, J 0.9), 8.73 (1H, s).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07005431B2 |
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| Source dataset | uspto-grants-2006_02 |
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| ORD ID | ord-bd11bcd6ae594eafb2d8970b7f820a1d |
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| Source note | uspto-grants-2006_02 |
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