4-(4-Morpholinophenyl)aminocarbonylbenzaldehyde → 4-(6-(4-Cyanobenzyloxy)-1H-benzo[d]imidazol-2-yl)-N-(4-morpholinophenyl)benzamide
反応式
[C:1]([C:3]1[CH:22]=[CH:21][C:6]([CH2:7][O:8][C:9]2[CH:14]=[CH:13][C:12]([N+:15]([O-])=O)=[C:11]([N+:18]([O-])=O)[CH:10]=2)=[CH:5][CH:4]=1)#[N:2].[O:23]1[CH2:28][CH2:27][N:26]([C:29]2[CH:34]=[CH:33][C:32]([NH:35][C:36]([C:38]3[CH:45]=[CH:44][C:41]([CH:42]=O)=[CH:40][CH:39]=3)=[O:37])=[CH:31][CH:30]=2)[CH2:25][CH2:24]1>>[C:1]([C:3]1[CH:22]=[CH:21][C:6]([CH2:7][O:8][C:9]2[CH:14]=[CH:13][C:12]3[N:15]=[C:42]([C:41]4[CH:40]=[CH:39][C:38]([C:36]([NH:35][C:32]5[CH:31]=[CH:30][C:29]([N:26]6[CH2:25][CH2:24][O:23][CH2:28][CH2:27]6)=[CH:34][CH:33]=5)=[O:37])=[CH:45][CH:44]=4)[NH:18][C:11]=3[CH:10]=2)=[CH:5][CH:4]=1)#[N:2]参加物
3
実験手順
Compound 641 was prepared according to the procedure similar to that described in Scheme III from 1-(4-cyanobenzyloxy)-3,4-dinitrobenzene and 4-(4-(4-morpholinophenyl)aminocarbonylbenzaldehyde. [M+H]+ calcd for C32H27N5O3: 530.21; found: 530.10.
出典と根拠
- ORDレコード
- ord-20b1d94e018b4f4dbb6d469cfd9cbcf3
- 出典データセット
- uspto-grants-2015_09