Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1373828Generated: October 31, 2026

Potassium Fluoride → 2-(4-Fluorophenyl)-3-(4-pyridinyl)pyrazolo[1,5-a]pyridine

https://huagongshe.com/reaction/1373828

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium FluorideHCID 522689—
Reactant4-(Tri-n-butylstannyl)pyridineHCID 2737318—
Reactant2-(4-Fluorophenyl)-3-bromopyrazolo[1,5-a]pyridineHCID 21948678—
CatalystHCID 178418397HCID 178418397—
SolventTolueneHCID 1140—
SolventDiethyl EtherHCID 3283—
Product2-(4-Fluorophenyl)-3-(4-pyridinyl)pyrazolo[1,5-a]pyridineHCID 9857146—

Reaction Steps

To a solution of 2-(4-fluorophenyl)-3-bromopyrazolo[1,5-α]pyridine (0.2 g, 0.68 mmol) and 4-(tributylstannyl)pyridine (0.38 g, 1 mmol) in dry toluene (10 mL) was added tetrakis(triphenylphosphine)palladium (0) (0.03 g, 0.03 mmol) and the mixture was heated at reflux temperature under a nitrogen atmosphere for about 48 hours. The mixture was cooled to room temperature and diluted with diethyl ether (40 mL). The mixture was poured into a 10% aqueous solution of potassium fluoride (20 mL) and the mixture was stirred for 1 hour. The biphasic mixture was filtered through a pad of diatomaceous earth and the organic phase was separated. The aqueous phase was extracted with diethyl ether (10 mL) and the combined organic phases are washed with brine, dried over anhydrous magnesium sulfate, filtered and the solvent evaporated under reduced pressure. The residue was purified using silica gel chromatography with 20% ethyl acetate in hexanes, followed by 50% ethyl acetate in hexanes, as eluent to give the title compound as an off white solid, 0.16 g (80%). 1H NMR (CDCl3) δ 8.58 (br s, 2H), 8.50 (d, 1H, J=7.2 Hz), 7.63 (d, 1H, 9 Hz), 7.52 (m, 2H), 7.27–7.20 (m, 3H), 7.06 (t, 2H, 8.7 Hz), 6.86 dt, 1H, J=7, 1 Hz). MS (+ve ion electrospray) 290 (100), (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07163940B2
Source datasetuspto-grants-2007_01
ORD IDord-011bd4f3af484060b5c45a3071a60fc2
Source noteuspto-grants-2007_01