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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 377619Generated: October 25, 2026

2-(Phenylamino)benzonitrile → Ethyl 4-amino-2-oxo-1-phenyl-1,2-dihydro-quinoline-3-carboxylate

https://huagongshe.com/reaction/377619

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(Phenylamino)benzonitrileHCID 252880—
ReactantPropanedioic acid, monoethyl esterHCID 3595298—
ReactantSodiumHCID 5360545—
ReactantEthanol sodium ethoxideHCID 23706232—
SolventEthanolHCID 702—
ProductEthyl 4-amino-2-oxo-1-phenyl-1,2-dihydro-quinoline-3-carboxylateHCID 1935622151.7%

Reaction Steps

Into a sodium ethoxide/ethanol solution which had been prepared from 2.07 g (90 mmol) of metallic sodium and 75 ml of anhydrous ethanol, 14.4 g (90 mmol) of ethyl malonate were added dropwise at room temperature. After the resultant mixture was stirred for 30 minutes as was, 5.82 g (30 mmol) of 2-phenylaminobenzonitrile were added and the mixture so obtained was heated under reflux for 48 hours. The reaction mixture was concentrated under reduced pressure, followed by the addition of ethyl acetate. The resulting solution was washed with water and was then dried. The solvent was distilled off under reduced pressure. The residue was purified by chromatography on a silica gel column and was then recrystallized from chloroform/hexane, whereby 4.78 g of ethyl 4-amino-2-oxo-1-phenyl-1,2-dihydro-quinoline-3-carboxylate (Compound No. 1) were obtained (yield: 51.7%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06028081
Source datasetuspto-grants-2000_02
ORD IDord-032e1a16f50b49e68f874f7e59ca4e90
Source noteuspto-grants-2000_02