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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1374708Generated: October 29, 2026

Sodium Carbonate → 3-(2,6-Difluoro-4-pyridinyl)-2-(4-fluorophenyl)pyrazolo[1,5-a]pyridine

https://huagongshe.com/reaction/1374708

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant2,6-Difluoropyridine-4-boronic acidHCID 2762747—
Reactant2-(4-Fluorophenyl)-3-bromopyrazolo[1,5-a]pyridineHCID 21948678—
CatalystHCID 178418476HCID 178418476—
SolventDimethylformamideHCID 6228—
Product3-(2,6-Difluoro-4-pyridinyl)-2-(4-fluorophenyl)pyrazolo[1,5-a]pyridineHCID 985845325.1%

Reaction Steps

A solution of 3-bromo-2-(4-fluorophenyl)-pyrazolo[1,5-a]pyridine (from Example le, 570 mg, 1.96 mmol), 2,6-difluoro-4-pyridyl-boronic acid (340 mg, 2.15 mmol) and dichlorobis(triphenylphosphine)palladium (137 mg, 0.196 mmol) in DMF (10.0 mL) was placed in a pre-heated oil bath at 110° C. To the reaction was added, in a dropwise manner, 2M sodium carbonate (2.00 mL, 4.00 mmol). The reaction was allowed to stir for 45 min before cooling to room temperature and filtering through a Celite 545 pad. The Celite filter was washed with ethyl acetate and the filtrate was concentrated to dryness at 50° C. under vacuum. The residue was dissolved in methylene chloride and dried (MgSO4). The drying agent was removed by filtration and the filtrate was concentrated and purified by silica gel chromatography to yield the title compound (160 mg, 0.492 mmol, 25%). 1H NMR (CDCl3) δ 8.53(d, 1H, J=6.8 Hz), 7.67(d, 1H, J=8.8 Hz), 7.53(dd, 2H, J=5.6, 8.0 Hz), 7.31(t, 1H, J=7.6 Hz), 7.11(t, 2H, J=8.4 Hz), 6.93(t, 1H, J=6.8 Hz), 6.75(s, 2H). MS (ES+ve): 326 (90, M+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07166597B2
Source datasetuspto-grants-2007_01
ORD IDord-96215039734a4d5694ec23d25c02db3a
Source noteuspto-grants-2007_01