반응식
CO[C:3]1[C:12]2[C:7](=[C:8]([CH3:20])[C:9]3[NH:15][C:14]4[CH:16]=[CH:17][N:18]=[CH:19][C:13]=4[C:10]=3[CH:11]=2)[CH:6]=[CH:5][N:4]=1.[Cl:21]P(=O)(Cl)C1C=CC=CC=1.[OH-].[Na+]>>[Cl:21][C:3]1[C:12]2[C:7](=[C:8]([CH3:20])[C:9]3[NH:15][C:14]4[CH:16]=[CH:17][N:18]=[CH:19][C:13]=4[C:10]=3[CH:11]=2)[CH:6]=[CH:5][N:4]=1참가 물질
4
반응 조건
- 온도
- 160 °C
실험 절차
1.053 g (0.004 mole) of 10-methoxy 6-methyl 5H-pyrido[3',4':4,5]pyrrolo[2,3-g]isoquinoline are suspended in 5.6 ml (0.040 mole) of dichlorophenylphosphine oxide and the suspension is heated at 160° C. for 2 hours. The reaction mixture is poured onto ice and the pH is brought to 7 by the addition of 10N sodium hydroxide. After filtration and drying of the precipitate formed, 0.580 g of 10-chloro 6-methyl 5H-pyrido[3',4':4,5]pyrrolo[2,3-g]isoquinoline are obtained.
후처리
- additionThe reaction mixture is poured onto ice
- filtrationAfter filtration
- customdrying of the precipitate
- customformed
출처 및 근거
- ORD 기록
- ord-08169c61c9704b24a6bef8b60afbebe0
- 출처 데이터셋
- uspto-grants-1992_01
- 특허 번호
- US05079363
연결된 노트
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