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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 587431Generated: October 31, 2026

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

https://huagongshe.com/reaction/587431

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 numberUS09226921B2
Source datasetuspto-grants-2016_01
ORD IDord-7f6b6f69761344e19675083e1129a303
Source noteuspto-grants-2016_01