m-Chloroperbenzoic acid → 2-Phenyl-pyrrolo[3,4-c]quinoline-3(1H),4(5H)-dione
반응식
[C:1]1([N:7]2[CH2:19][C:18]3[C:17]4[CH:16]=[CH:15][CH:14]=[CH:13][C:12]=4[N:11]=[CH:10][C:9]=3[C:8]2=[O:20])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.ClC1C=CC=C(C(OO)=[O:29])C=1>C(Cl)Cl>[C:1]1([N:7]2[CH2:19][C:18]3[C:17]4[CH:16]=[CH:15][CH:14]=[CH:13][C:12]=4[NH:11][C:10](=[O:29])[C:9]=3[C:8]2=[O:20])[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=1참가 물질
반응 조건
- 온도
- 50 °C
실험 절차
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.
후처리
- washwashed with sodium carbonate solution
- dry with materialThe organic layer was dried over magnesium sulfate
- customthe solvent was removed in vacuo
- customThe reaction was quenched with methanol
- concentrationThe reaction mixture was concentrated in vacuo
- extractionthe resulting aqueous solution was extracted with ethyl acetate
- dry with materialthe organic layer was dried over magnesium sulfate
- customthe solvent was removed in vacuo
- customThe residue was triturated with ether
출처 및 근거
- ORD 기록
- ord-1d6ca19c2d34480a8b08a5ba2eeccaa4
- 출처 데이터셋
- uspto-grants-1997_02
- 특허 번호
- US05604235
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