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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 640718Generated: October 31, 2026

Allyl iodide → 2-(Allyloxy)-4-(3-fluorophenyl)-6-methoxyquinoline-3-carbonitrile

https://huagongshe.com/reaction/640718

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl iodideHCID 11166—
ReactantSodium hydrideHCID 24758—
Reactant4-(3-Fluorophenyl)-6-methoxy-2-oxo-1,2-dihydroquinoline-3-carbonitrileHCID 11415165—
SolventDimethylformamideHCID 6228—
Product2-(Allyloxy)-4-(3-fluorophenyl)-6-methoxyquinoline-3-carbonitrileHCID 11404847—

Reaction Steps

To a solution of 4-(3-fluorophenyl)-6-methoxy-2-oxo-1,2-dihydroquinoline-3-carbonitrile (1.00 g, 3.40 mmol) in 20 mL of N,N-dimethylformamide at 0° C. was added sodium hydride (163 mg of 60% dispersion in mineral oil, 4.08 mmol). After 30 minutes, allyl iodide was added (0.342 mL, 3.74 mmol), and the reaction was stirred for 2 hours. The reaction was quenched with water and partitioned between EtOAc and water, and the organic layer was washed with brine, dried over Na2SO4, filtered, and concentrated in vacuo. The crude residue was subjected to flash chomatography through SiO2 (5-60% EtOAc/hexane) to provide the second eluting product as the titled compound. 1H NMR, difference nOe, and HMQC NMR spectral data for the product were consistent with the titled compound. ESI+ MS: 335.1 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07692017B2
Source datasetuspto-grants-2010_04
ORD IDord-20b30a7b552c40d2a652fd6f80353e4c
Source noteuspto-grants-2010_04