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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethanol, 2-(aminooxy)-, hydrochloride | HCID 22507086 | — |
| Reactant | 1-(1-(1-(5,7-Difluoroquinolin-6-yl)ethyl)-1H-[1,2,3]triazolo[4,5-b]pyrazin-6-yl)ethanone | HCID 58190554 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 2-[(E)-1-[3-[1-(5,7-difluoroquinolin-6-yl)ethyl]triazolo[4,5-b]pyrazin-5-yl]ethylideneamino]oxyethanol | HCID 58190538 | 63.8% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08507676B2 |
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| Source dataset | uspto-grants-2013_08 |
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| ORD ID | ord-d8e354d5303e43a1b8236060c342da46 |
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| Source note | uspto-grants-2013_08 |
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