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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 466007Generated: October 29, 2026

Ethanol → 3-(2-Phenylpyrazolo[1,5-a]pyridin-3-yl)-2-hydroxyiminopropionic acid

https://huagongshe.com/reaction/466007

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantPotassium HydroxideHCID 14797—
ReactantHydroxyamine hydrochlorideHCID 443297—
Reactant3-(2-Phenylpyrazolo[1,5-a]pyridin-3-yl)-2-thioxopropionic acidHCID 15158173—
SolventWaterHCID 962—
Product3-(2-Phenylpyrazolo[1,5-a]pyridin-3-yl)-2-hydroxyiminopropionic acidHCID 5367942869.8%

Reaction Steps

A mixture of 3-(2-phenylpyrazolo[1,5-a]pyridin-3-yl)-2-thioxopropionic acid (3.74 g), hydroxylamine hydrochloride (2.63 g), 85% potassium hydroxide (2.50 g) and 80% aqueous ethanol (22.4 ml) was refluxed for 3 hours. After cooling, to the reaction mixture was added water (40 ml) and the resulting precipitates were filtered off. The filtrate was washed with methylene chloride (20 ml) twice, acidified with 10% aqueous hydrochloric acid (pH≈2), and extracted with ethyl acetate (20 ml) twice. The organic layer was washed with water (10 ml) and a saturated aqueous solution of sodium chloride and dried over magnesium sulfate. The solvent was removed to give 3-(2-phenylpyrazolo[1,5-a]pyridin-3-yl)-2-hydroxyiminopropionic acid (2.60 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05155114
Source datasetuspto-grants-1992_10
ORD IDord-acd8396db8fa4c719e29254af4576e6f
Source noteuspto-grants-1992_10