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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1415717Generated: November 2, 2026

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

https://huagongshe.com/reaction/1415717

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 numberUS05908932
Source datasetuspto-grants-1999_06
ORD IDord-589e496fb2124902a29c539e315a3cda
Source noteuspto-grants-1999_06