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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1892387Generated: October 31, 2026

Ethanol, 2-(aminooxy)- → HCID 50991634, compound

https://huagongshe.com/reaction/1892387

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanol, 2-(aminooxy)-HCID 3014186—
Reactant1-(3-(Difluoro(quinolin-6-yl)methyl)-[1,2,4]triazolo[4,3-b]pyridazin-6-yl)ethanoneHCID 58190468—
SolventMethanolHCID 887—
ProductHCID 50991634HCID 5099163455.3%

Reaction Steps

A solution of 1-(3-(difluoro(quinolin-6-yl)methyl)-[1,2,4]triazolo[4,3-b]pyridazin-6-yl)ethanone (54 mg, 0.159 mmol) and 2-(aminooxy)ethanol (intermediate S) (36.1 mg, 0.318 mmol) in 8 mL of MeOH was stirred at it overnight. Solvent was evaporated and the residue was partitioned between water and EtOAc. Aqueous layer was extracted with EtOAc twice. Organic layers were combined, washed with brine and dried over Na2SO4. Solvent was evaporated and the crude was purified by HPLC (basic with 0.05% NH4OH) to give 35 mg (55%) of the title compound as a white solid. 1H-NMR (400 MHz, MeOH-d4) δ ppm 8.98 (d, 1H), 8.52 (d, 1H), 8.43 (s, 1H), 8.23 (d, 1H), 8.19 (d, 1H), 8.06 (d, 1H), 8.04 (d, 1H), 7.66 (m, 1H), 4.36 (m, 2H), 3.84 (m, 2H), 2.18 (s, 3H). LCMS (method B): [MH]+=398.9, tR=2.29 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08507676B2
Source datasetuspto-grants-2013_08
ORD IDord-83462306c9be47ffba1b74e5f376ebf1
Source noteuspto-grants-2013_08