Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 347694Generated: October 27, 2026

Ethanol → 3-Trifluoromethyl-imidazo[1,2-B][1,2,4]triazine

https://huagongshe.com/reaction/347694

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantEthane, 2-bromo-1,1-diethoxy-HCID 74852—
ReactantSodium BicarbonateHCID 516892—
Reactant5-(Trifluoromethyl)-1,2,4-triazin-3-amineHCID 11542832—
SolventHydrogen BromideHCID 260—
SolventWaterHCID 962—
Product3-Trifluoromethyl-imidazo[1,2-B][1,2,4]triazineHCID 1162246922.5%

Reaction Conditions

Temperature60 °C

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, J 0.8), 8.30 (1H, d, J 0.9), 8.73 (1H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07176203B2
Source datasetuspto-grants-2007_02
ORD IDord-1168689260204daf8fc2fa27cab32373
Source noteuspto-grants-2007_02