HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 586227Generated: October 29, 2026
Ethanol → 3-(1-Fluoro-1-methylethyl)imidazo[1,2-b][1,2,4]triazine
https://huagongshe.com/reaction/586227
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Ethane, 2-bromo-1,1-diethoxy- | HCID 74852 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 3-Amino-5-(1-fluoro-1-methylethyl)-1,2,4-triazine | HCID 22240088 | — |
| Solvent | Hydrogen Bromide | HCID 260 | — |
| Solvent | Water | HCID 962 | — |
| Product | 3-(1-Fluoro-1-methylethyl)imidazo[1,2-b][1,2,4]triazine | HCID 22240098 | 17.3% |
Reaction Steps
A stirred mixture of bromoacetaldehyde diethyl acetal (1.20 ml, 7.73 mmol) in concentrated hydrobromic acid (0.38 ml) and water (0.38 ml) was heated at reflux for 40 min, then poured into ethanol (3 ml). The solution was neutralised to pH 7 with solid sodium hydrogencarbonate, then filtered, washing the solid with more ethanol (3 ml). To the filtrate was added 3-amino-5-(1-fluoro-1-methylethyl)-1,2,4-triazine (1.0046 g, 6.43 mmol) and the mixture was stirred at 70-80° C. for 17 h. The mixture was evaporated in vacuo, and the residue was purified by flash chromatography (silica gel, 70% EtOAc/isohexane to 15% MeOH/EtOAc, then 20% EtOAc/CH2Cl2) to give 0.2000 g (17%) of the title compound as a pale yellow solid: 1H NMR (360 MHz, CDCl3) δ 1.82 (6H, d, J 22.1 Hz), 7.97 (1H, d, J 1.3 Hz), 7.99 (1H, d, J 1.2 Hz), 8.69 (1H, d, J 1.0 Hz).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06936608B2 |
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| Source dataset | uspto-grants-2005_08 |
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| ORD ID | ord-426e69cf3a124ad982249bf497a080d4 |
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| Source note | uspto-grants-2005_08 |
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