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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1892439Generated: October 28, 2026

Ethanol, 2-(aminooxy)-, hydrochloride → 2-[(E)-1-[3-[1-(5,7-difluoroquinolin-6-yl)ethyl]triazolo[4,5-b]pyrazin-5-yl]ethylideneamino]oxyethanol

https://huagongshe.com/reaction/1892439

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanol, 2-(aminooxy)-, hydrochlorideHCID 22507086—
Reactant1-(1-(1-(5,7-Difluoroquinolin-6-yl)ethyl)-1H-[1,2,3]triazolo[4,5-b]pyrazin-6-yl)ethanoneHCID 58190554—
SolventMethanolHCID 887—
Product2-[(E)-1-[3-[1-(5,7-difluoroquinolin-6-yl)ethyl]triazolo[4,5-b]pyrazin-5-yl]ethylideneamino]oxyethanolHCID 5819053863.8%

Reaction Conditions

Temperature45 °C

Reaction Steps

To a solution of 1-(1-(1-(5,7-difluoroquinolin-6-yl)ethyl)-1H-[1,2,3]triazolo[4,5-b]pyrazin-6-yl)ethanone (76.5 mg, 0.22 mmol) in MeOH (50 mL) was added 2-(aminooxy)ethanol hydrochloride (49.0 mg, 0.43 mol). The mixture was heated at 45° C. overnight. The solvent was removed under reduced pressure. The residue was purified by column chromatography with gradient (DCM/MeOH=10:1) to give the title compound as a white solid (58.0 mg, 62%). 1H-NMR (400 MHz, DMSO-d6) δ ppm 9.23 (s, 1H), 9.01 (dd, 1H), 8.52 (d, 1H), 7.74 (d, 1H), 7.63 (dd, 1H), 6.80 (q, 1H), 4.74 (t, 1H), 4.27 (t, 2H), 3.68 (m, 2H), 2.36 (d, 3H), 2.10 (s, 3H). LCMS (method A): [MH]+=414, tR=5.44 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08507676B2
Source datasetuspto-grants-2013_08
ORD IDord-d8e354d5303e43a1b8236060c342da46
Source noteuspto-grants-2013_08