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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetohydroxamic Acid | HCID 1990 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3-Fluoro-4-(4-methyl-3-pyridinyl)pyridine-2-carbonitrile | HCID 86730402 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 7-(4-Methylpyridin-3-yl)isoxazolo[4,5-b]pyridin-3-amine | HCID 86730405 | 77.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09242967B2 |
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| Source dataset | uspto-grants-2016_01 |
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| ORD ID | ord-b59121337c564839b76c0882000208e6 |
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| Source note | uspto-grants-2016_01 |
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