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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 408802Generated: October 27, 2026

Potassium Carbonate → 3-(3,5-Difluorophenyl)-2-ethylpyrazolo[1,5-a]pyridine

https://huagongshe.com/reaction/408802

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant(3,5-Difluorophenyl)boronic acidHCID 2734338—
Reactant2-Ethyl-3-iodopyrazolo[1,5-a]pyridineHCID 16114933—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
Solvent1,4-DioxaneHCID 31275—
Product3-(3,5-Difluorophenyl)-2-ethylpyrazolo[1,5-a]pyridineHCID 5837933480%

Reaction Conditions

Temperature100 °C

Reaction Steps

2-Ethyl-3-iodopyrazolo[1,5-a]pyridine (0.5 g, 2.0 mmol) and (3,5-difluorophenyl)boronic acid (0.35 g, 2.2 mmol) [Aldrich 471925] were stirred in dioxane (12 mL). A solution of potassium carbonate (0.29 g, 2.1 mmol) in water (2.8 mL) was added. Tetrakis-(triphenylphosphine)palladium(0) (0.13 g, 0.1 mmol) was added and the mixture was heated at 100° C. for 16 h. After cooling, the mixture was diluted with ethyl acetate and washed with water and brine. The extracts were dried over magnesium sulfate, filtered, concentrated and purified on silica gel with ethyl acetate in hexanes (0-10%) to give the desired compound (0.41 g, 80%). LCMS for C15H13F2N2 (M+H)+: m/z=259.2. 1H NMR (300 MHz, DMSO-d6): δ 8.67 (m, 1H), 7.64 (m, 1H), 7.25 (m, 1H), 7.18 (m, 3H), 6.90 (m, 1H), 2.89 (m, 2H), 1.22 (m, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08759359B2
Source datasetuspto-grants-2014_06
ORD IDord-50cdc95021744e579493276c99fbd4b0
Source noteuspto-grants-2014_06