2-Methoxybenzaldehyde → HCID 25235532、化合物
反応式
Cl[C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][CH:11]=1)[N:8]=[C:7]([NH2:12])[CH:6]=[C:5]2[C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1.[CH3:19][O:20][C:21]1[CH:28]=[CH:27][CH:26]=[CH:25][C:22]=1[CH:23]=O.[CH3:29][O:30][C:31]1[CH:38]=[CH:37][CH:36]=[CH:35][C:32]=1[CH2:33][NH2:34]>>[CH3:19][O:20][C:21]1[CH:28]=[CH:27][CH:26]=[CH:25][C:22]=1[CH2:23][NH:12][C:7]1[CH:6]=[C:5]([C:13]2[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=2)[C:4]2[C:9](=[CH:10][CH:11]=[C:2]([NH:34][CH2:33][C:32]3[CH:35]=[CH:36][CH:37]=[CH:38][C:31]=3[O:30][CH3:29])[CH:3]=2)[N:8]=1参加物
4
実験手順
The title compound, MS: m/e=476.3 (M+H+), was prepared in accordance with the general method of example 13 from 6-chloro-4-phenyl-quinolin-2-ylamine (CAS 51478-40), 2-methoxybenzaldehyde and 2-methoxybenzylamine.
出典と根拠
- ORDレコード
- ord-cb729c59cba7489da2985bff8736ad3d
- 出典データセット
- uspto-grants-2013_03