6-Methoxy-8-quinolinamine → N-(6-methoxyquinolin-8-yl)-4-methyl-2-nitrobenzenesulfonamide
反応式
[CH3:1][O:2][C:3]1[CH:4]=[C:5]2[C:10](=[C:11]([NH2:13])[CH:12]=1)[N:9]=[CH:8][CH:7]=[CH:6]2.[N+:14]([C:17]1[CH:22]=[C:21]([CH3:23])[CH:20]=[CH:19][C:18]=1[S:24](Cl)(=[O:26])=[O:25])([O-:16])=[O:15]>>[CH3:1][O:2][C:3]1[CH:4]=[C:5]2[C:10](=[C:11]([NH:13][S:24]([C:18]3[CH:19]=[CH:20][C:21]([CH3:23])=[CH:22][C:17]=3[N+:14]([O-:16])=[O:15])(=[O:25])=[O:26])[CH:12]=1)[N:9]=[CH:8][CH:7]=[CH:6]2参加物
3
実験手順
In a similar fashion using route 14 general procedure 26, 6-methoxyquinolin-8-amine (Intermediate 23) (120 mg, 0.69 mmol) and 4-methyl-2-nitrobenzenesulfonyl chloride (Intermediate 20) (186 mg, 1.03 mmol) gave the title compound (150 mg, 58%) after purification by column chromatography with DCM as the eluent.
出典と根拠
- ORDレコード
- ord-eda6e5b1ee484c98ac736c33d49651ee
- 出典データセット
- uspto-grants-2015_08