HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 5133Generated: October 28, 2026
m-Chloroperbenzoic acid → 2-Phenyl-pyrrolo[3,4-c]quinoline-3(1H),4(5H)-dione
https://huagongshe.com/reaction/5133
Participants
| Role | Name | HCID | Charge |
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| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | HCID 57023940 | HCID 57023940 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-Phenyl-pyrrolo[3,4-c]quinoline-3(1H),4(5H)-dione | HCID 13811780 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05243049 |
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| Source dataset | uspto-grants-1993_09 |
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| ORD ID | ord-85ced26261244ccdada566c55d307030 |
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| Source note | uspto-grants-1993_09 |
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