Acetic Acid → 4-(3-Aminocarbonyl-2-methylanilino)-6,7-dimethoxy-3-quinolinecarboxamide
반응식
Cl[C:2]1[C:11]2[C:6](=[CH:7][C:8]([O:14][CH3:15])=[C:9]([O:12][CH3:13])[CH:10]=2)[N:5]=[CH:4][C:3]=1[C:16]([NH2:18])=[O:17].[NH2:19][C:20]1[C:21]([CH3:29])=[C:22]([CH:26]=[CH:27][CH:28]=1)[C:23]([NH2:25])=[O:24].C(O)(=O)C.[OH-].[Na+]>CN(C=O)C.O>[NH2:25][C:23]([C:22]1[C:21]([CH3:29])=[C:20]([CH:28]=[CH:27][CH:26]=1)[NH:19][C:2]1[C:11]2[C:6](=[CH:7][C:8]([O:14][CH3:15])=[C:9]([O:12][CH3:13])[CH:10]=2)[N:5]=[CH:4][C:3]=1[C:16]([NH2:18])=[O:17])=[O:24]참가 물질
7
반응 조건
- 온도
- 100 °C
실험 절차
A mixture of 4-chloro-6,7-dimethoxy-3-quinolinecarboxamide (0.046 g, 0.17 mmol), 3-amino 2-metylbenzamide (0.036 g, 0.24 mmol) and acetic acid (40 μl) in DMF (0.8 ml) was heated at 100° C. for 18 h. After cooling the reaction mixture was diluted with water (20 ml) and made alkaline with 1 M NaOH. The precipitate was filtered of, rinsed with water and dried to give the title compound (41 mg, 61%).
후처리
- temperatureAfter cooling the reaction mixture
- filtrationThe precipitate was filtered of,
- washrinsed with water
- customdried
출처 및 근거
- ORD 기록
- ord-0e0e4ca10d7b45ffa48a5b9c49223386
- 출처 데이터셋
- uspto-grants-2006_05
- 특허 번호
- US07037925B2
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