2-Chloro-5-nitroquinoline → N-(2-{[(5-methyl-2-furyl)methyl]amino}quinolin-5-yl)-N'-(4-fluorophenyl)sulfamide
反応式
[N+:1]([C:4]1[CH:13]=[CH:12][CH:11]=[C:10]2[C:5]=1[CH:6]=[CH:7][C:8](Cl)=[N:9]2)([O-])=O.[CH3:15][C:16]1[O:20][C:19]([CH2:21][NH2:22])=[CH:18][CH:17]=1.[F:23][C:24]1[CH:29]=[CH:28][C:27]([NH:30][S:31](Cl)(=[O:33])=[O:32])=[CH:26][CH:25]=1>>[CH3:15][C:16]1[O:20][C:19]([CH2:21][NH:22][C:8]2[CH:7]=[CH:6][C:5]3[C:10](=[CH:11][CH:12]=[CH:13][C:4]=3[NH:1][S:31]([NH:30][C:27]3[CH:26]=[CH:25][C:24]([F:23])=[CH:29][CH:28]=3)(=[O:32])=[O:33])[N:9]=2)=[CH:18][CH:17]=1参加物
4
実験手順
The title compound, MS: m/e=427.3 (M+H+), was prepared in accordance with the general method of example 58 from 5-nitro-2-chloroquinoline, 5-methyl-2-furanmethanamine and 4-fluoro-phenylsulfamoyl chloride.
出典と根拠
- ORDレコード
- ord-09ff0cca580641268110687433b76796