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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1416670Generated: October 30, 2026

Aniline → 1-(Phenyl)-4-oxo-6-methoxy-2,3,4,5-tetrahydropyrrolo[3,2-c]quinoline

https://huagongshe.com/reaction/1416670

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAnilineHCID 6115—
Reactant4-Oxo-6-methoxy-2,3-dihydrofuro[3,2-c]quinolineHCID 67626099—
SolventWaterHCID 962—
SolventPhenolHCID 996—
Product1-(Phenyl)-4-oxo-6-methoxy-2,3,4,5-tetrahydropyrrolo[3,2-c]quinolineHCID 1580885382.1%

Reaction Conditions

Temperature190 °C

Reaction Steps

4-Oxo-6-methoxy-2,3-dihydrofuro[3,2-c]quinoline (217 mg, 1.0 mmol) was dissolved in 7 ml of phenol and aniline (228 μl, 2.5 mmol) was added under nitrogen. The reaction mixture was heated at 190° C. for 15 hours. The reaction mixture was diluted with 20 ml of salt water and the aqueous layer was extracted with methylene chloride (15 ml×3). After washing with water (15 ml×3), the organic layer was dried by anhydrous magnesium surface and filtered, and concentrated under reduced pressure. The residue was purified with ethyl acetate as eluent by silica gel chromatography to obtain 240 mg of desired compound as solid in 83% of yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05914402
Source datasetuspto-grants-1999_06
ORD IDord-36e47219e5a74fd0ba239f883256b0d5
Source noteuspto-grants-1999_06