6-Methyl-2-pyridinecarboxaldehyde → N2-(5-Methyl-furan-2-ylmethyl)-N5-(6-methyl-pyridin-2-ylmethyl)-quinoline-2,5-diamine
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.[CH3:23][C:24]1[N:29]=[C:28]([CH:30]=O)[CH:27]=[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:4]([NH:1][CH2:30][C:28]4[CH:27]=[CH:26][CH:25]=[C:24]([CH3:23])[N:29]=4)=[CH:13][CH:12]=[CH:11][C:10]=3[N:9]=2)=[CH:18][CH:17]=1参加物
4
実験手順
The title compound, MS: m/e=359.1 (M+H+), was prepared from 5-nitro-2-chloroquinoline, 5-methyl-2-furanmethanamine and 6-methyl-2-pyridinecarboxaldehyde as described in example 26.
出典と根拠
- ORDレコード
- ord-3a4275e406de455ba7c20079574afe42
- 出典データセット