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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1478693Generated: October 31, 2026

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

https://huagongshe.com/reaction/1478693

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, 1 H), 7.64 (m, 1 H), 7.25 (m, 1 H), 7.18 (m, 3 H), 6.90 (m, 1 H), 2.89 (m, 2 H), 1.22 (m, 3 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09403847B2
Source datasetuspto-grants-2016_08
ORD IDord-58369dbe70c6489d8650b0eb66f0bcc7
Source noteuspto-grants-2016_08