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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1837337Generated: October 31, 2026

Ethanol → 4-Chloro-6-ethoxy-7-fluoro-3-quinolinecarbonitrile

https://huagongshe.com/reaction/1837337

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantTriphenylphosphineHCID 11776—
ReactantDiethyl azodicarboxylateHCID 5462977—
Reactant4-Chloro-7-fluoro-6-hydroxy-3-quinolinecarbonitrileHCID 23498076—
SolventTetrahydrofuranHCID 8028—
Product4-Chloro-6-ethoxy-7-fluoro-3-quinolinecarbonitrileHCID 23498102—

Reaction Steps

To a 0° C. mixture of 4-chloro-7-fluoro-6-hydroxy-3-quinolinecarbonitrile (185 mg, 0.83 mmol), triphenylphosphine (392 mg, 1.49 mmol) and ethanol (153 mg, 3.32 mmol) in 15 mL of tetrahydrofuran is added diethylazodicarboxylate (260 mg, 1.80 mmol). The reaction mixture is kept at 0° C. for 45 minutes then stirred at room temperature overnight. The reaction mixture is concentrated in vacuo and purified by flash column chromatography eluting with a gradient of 1 % ethyl acetate in hexane to 5% ethyl acetate in hexane provides 4-chloro-6-ethoxy-7-fluoro-3-quinolinecarbonitrile, mp 165-166° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06780996B2
Source datasetuspto-grants-2004_08
ORD IDord-eea85c27c7704985b171c5b53ff0b0e0
Source noteuspto-grants-2004_08