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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1451291Generated: October 30, 2026

m-Chloroperbenzoic acid → 2-Phenyl-pyrrolo[3,4-c]quinoline-3(1H),4(5H)-dione

https://huagongshe.com/reaction/1451291

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantHCID 57023940HCID 57023940—
SolventDichloromethaneHCID 6344—
Product2-Phenyl-pyrrolo[3,4-c]quinoline-3(1H),4(5H)-dioneHCID 13811780—

Reaction Conditions

Temperature50 °C

Reaction Steps

A mixture of 2-Phenyl-pyrrolo[3,4-c]quinolin-3(1H)-one (60 mg), and m-chloroperbenzoic acid (105 mg) in 3 mL of methylene chloride was kept at room temperature for 24 h. The mixture was diluted with methylene chloride and washed with sodium carbonate solution. The organic layer was dried over magnesium sulfate and the solvent was removed in vacuo. The residue was heated at 50° C. for 3 h with 1 mL of acetic anhydride. The reaction was quenched with methanol and made basic with ammonium hydroxide. The reaction mixture was concentrated in vacuo, and the resulting aqueous solution was extracted with ethyl acetate, the organic layer was dried over magnesium sulfate and the solvent was removed in vacuo. The residue was triturated with ether to afford 2-Phenyl-pyrrolo[3,4-c]quinoline-3(1H),4(5H)-dione (Compound 16) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05604235
Source datasetuspto-grants-1997_02
ORD IDord-1d6ca19c2d34480a8b08a5ba2eeccaa4
Source noteuspto-grants-1997_02