Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1837329Generated: November 2, 2026

Biphenyl → 7-FLUORO-6-METHOXY-4-OXO-1,4-DIHYDROQUINOLINE-3-CARBONITRILE

https://huagongshe.com/reaction/1837329

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBiphenylHCID 7095—
ReactantDiphenyl EtherHCID 7583—
Reactant2-Propenoic acid, 2-cyano-3-ethoxy-, ethyl esterHCID 78943—
Reactant3-Fluoro-4-methoxyanilineHCID 581110—
SolventTolueneHCID 1140—
SolventHexaneHCID 8058—
SolventEthyl AcetateHCID 8857—
Product7-FLUORO-6-METHOXY-4-OXO-1,4-DIHYDROQUINOLINE-3-CARBONITRILEHCID 121507022.6%

Reaction Conditions

Temperature105 °C

Reaction Steps

A mixture of 3-fluoro-4-methoxyaniline (15.31 g, 108 mmol) and ethyl (ethoxymethylene)cyanoacetate (18.36 g, 108 mmol) in toluene is heated at 100-110° C. for 4.5 hours then cooled to room temperature. A 1:1 mixture of hexane and ethyl acetate is added and the mixture is cooled on an ice bath. The solids are collected washing with hexane to provide a first crop of 26.10 g and a second crop of 1.24 g. A 2.0 g portion of this material is added to 18 mL of a 3:1 mixture of diphenyl ether:biphenyl that is heated to reflux. This mixture is heated at reflux for 4 hours then cooled and poured into hexane. The solids are collected by filtration and washed with ethyl acetate and hexane to provide 624 mg of 7-fluoro-6-methoxy-4-oxo-1,4,-dihydro-3-quinolinecarbonitrile as a brown solid. The filtrate is concentrated, the residue is dissolved in ethyl acetate and hexane is added. The resultant solid is collected by filtration to give 1.07 g of 7-fluoro-6-methoxy-4-oxo-1,4-dihydro-3-quinolinecarbonitrile as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06780996B2
Source datasetuspto-grants-2004_08
ORD IDord-893fee5c2c06414f94fab4ce5a1ff024
Source noteuspto-grants-2004_08