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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1044150Generated: October 30, 2026

p-Fluoronitrobenzene → 1-(4-nitrophenyl)-1H-pyrazolo[3,4-b]pyridine

https://huagongshe.com/reaction/1044150

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-FluoronitrobenzeneHCID 9590—
ReactantCesium carbonateHCID 10796—
ReactantSodium hydrideHCID 24758—
Reactant1H-pyrazolo(3,4-b)pyridineHCID 2755850—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product1-(4-nitrophenyl)-1H-pyrazolo[3,4-b]pyridineHCID 58577249—

Reaction Steps

To a stirred solution of 1H-pyrazolo[3,4-b]pyridine (300 mg) in DMF (3.0 mL) was added sodium hydride (101 mg) (60% in mineral oil) with ice-cooling. The mixture was stirred at room temperature for 30 min, and then 1-fluoro-4-nitrobenzene (355 mg) was added. After stirring at room temperature for 2 h, the mixture was warmed up to 50° C. The mixture was stirred at 50° C. for 12 h. Cesium carbonate (821 mg) was added and the mixture was stirred at 100° C. for 12 h, and treated with water and AcOEt. The insoluble material was filtered off. The organic layer was separated and the aqueous layer was extracted with AcOEt. The organic layer was combined, dried over MgSO4 and concentrated in vacuo. The residue was used for the next reaction.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08563575B2
Source datasetuspto-grants-2013_10
ORD IDord-a7c9529ae6144f6eb6c603245cfe937f
Source noteuspto-grants-2013_10