Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2121367Generated: November 2, 2026

Ethanol → 3-(1-Fluoro-1-methylethyl)imidazo[1,2-b][1,2,4]triazine

https://huagongshe.com/reaction/2121367

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantEthane, 2-bromo-1,1-diethoxy-HCID 74852—
ReactantSodium BicarbonateHCID 516892—
Reactant3-Amino-5-(1-fluoro-1-methylethyl)-1,2,4-triazineHCID 22240088—
SolventHydrogen BromideHCID 260—
SolventWaterHCID 962—
Product3-(1-Fluoro-1-methylethyl)imidazo[1,2-b][1,2,4]triazineHCID 2224009817.3%

Reaction Conditions

Temperature75 °C

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) δ1.82 (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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06696444B2
Source datasetuspto-grants-2004_02
ORD IDord-58df843f947d4530aaa2ffbac0f1a229
Source noteuspto-grants-2004_02