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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1429887Generated: November 3, 2026

p-Fluoronitrobenzene → 3-(4-nitrophenyl)[1,3]oxazolo[4,5-b]pyridin-2(3H)-one

https://huagongshe.com/reaction/1429887

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-FluoronitrobenzeneHCID 9590—
ReactantSodium hydrideHCID 24758—
ReactantOxazolo(4,5-b)pyridin-2(3H)-oneHCID 2799900—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product3-(4-nitrophenyl)[1,3]oxazolo[4,5-b]pyridin-2(3H)-oneHCID 5857763419.3%

Reaction Steps

A solution of oxazolo[4,5-b]pyridin-2(3H)-one (200 mg) in DMF (3.5 mL) was treated with a 60% dispersion of sodium hydride in mineral oil (62 mg) and the resulting mixture stirred at ambient temperature for 5 min. The mixture was treated with 1-fluoro-4-nitrobenzene (248 mg) then stirred at 100° C. for 17 h. After this time, the reaction mixture was cooled to ambient temperature, diluted with ethyl acetate (100 mL), washed with water (2×50 mL), 5% aqueous lithium chloride (50 mL) then brine (50 mL), dried over sodium sulfate, and filtered and the filtrate was concentrated under reduced pressure. The residue obtained was purified by chromatography (silica, heptane to 1:1 ethyl acetate/heptane) to afford 3-(4-nitrophenyl)[1,3]oxazolo[4,5-b]pyridin-2(3H)-one (73 mg) as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08940758B2
Source datasetuspto-grants-2015_01
ORD IDord-948ca18536704351b06848ad7e97a344
Source noteuspto-grants-2015_01