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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1802763Generated: November 1, 2026

Potassium Carbonate → 2-(1-Hydroxy-1-methyl-ethyl)-pyrazolo[1,5-a]pyridine-3-carboxylic acid ethyl ester

https://huagongshe.com/reaction/1802763

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantPyridinium, 1-amino-, iodide (1:1)HCID 2733704—
Reactant4-Hydroxy-4-methyl-pent-2-ynoic acid ethyl esterHCID 11228926—
SolventDimethylformamideHCID 6228—
Product2-(1-Hydroxy-1-methyl-ethyl)-pyrazolo[1,5-a]pyridine-3-carboxylic acid ethyl esterHCID 5789926477.3%

Reaction Steps

To a suspension of 1-amino-pyridinium iodide (0.343 g, 1.54 mmol) and potassium carbonate (0.278 g, 2.01 mmol) in 2 mL N,N-dimethylformamide was added 4-hydroxy-4-methyl-pent-2-ynoic acid ethyl ester (0.262 g, 1.70 mmol) in 1 mL N,N-dimethylformamide dropwise. The mixture was stirred at room temperature for 24 h under nitrogen atmosphere, poured on to ice and filtered, and the solid was washed with water to provide the crude product as a brown solid. The filtrate was extracted with ethyl acetate and the previously filtered solid was combined with the organic extracts, which was dried over magnesium sulfate, filtered and concentrated in vacuo and the residue was purified via silica gel column chromatography (0-50% ethyl acetate in heptane) to obtain the product as a yellow solid (0.296 g, 1.19 mmol, 77% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08349883B2
Source datasetuspto-grants-2013_01
ORD IDord-a7a11646bc1f4db0be078cca6f468a20
Source noteuspto-grants-2013_01