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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 593749Generated: October 29, 2026

Acetohydroxamic Acid → 7-(4-Methylpyridin-3-yl)isoxazolo[4,5-b]pyridin-3-amine

https://huagongshe.com/reaction/593749

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetohydroxamic AcidHCID 1990—
ReactantPotassium CarbonateHCID 11430—
Reactant3-Fluoro-4-(4-methyl-3-pyridinyl)pyridine-2-carbonitrileHCID 86730402—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product7-(4-Methylpyridin-3-yl)isoxazolo[4,5-b]pyridin-3-amineHCID 8673040577.2%

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of 3′-fluoro-4-methyl-3,4′-bipyridine-2′-carbonitrile (0.057 g, 0.267 mmol), N-hydroxyacetamide (0.060 g, 0.802 mmol), and potassium carbonate (0.222 g, 1.604 mmol) in DMF (Ratio: 7.0, Volume: 1.170 ml) and water (Ratio: 1.000, Volume: 0.167 ml) was stirred at 80° C. for 3 hr. The reaction mixture was filtered through a disposable fritted funnel. The filter cake was washed with EtOAc. Layers in the filtrate were separated and the aqueous phase was extracted with EtOAc (3×). The organic phases were combined, dried over Na2SO4, filtered, concentrated, and further dried under high vacuum to afford the title compound as a brown solid (49 mg, 0.206 mmol, 77% yield). ESI MS (M+H)+=227.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09242967B2
Source datasetuspto-grants-2016_01
ORD IDord-b59121337c564839b76c0882000208e6
Source noteuspto-grants-2016_01