反応式
[NH2:1][C:2]1[CH:11]=[C:10](O)[C:9]2[C:4](=[CH:5][CH:6]=[C:7](Cl)[CH:8]=2)[N:3]=1.C1(C)C=CC=C[C:15]=1[C:20]1[CH:25]=[CH:24][CH:23]=[CH:22][C:21]=1B(O)O.[CH3:30][O:31][C:32]1[CH:39]=[CH:38][CH:37]=[CH:36][C:33]=1[CH:34]=O.[N:40]1[CH:45]=[CH:44][CH:43]=[C:42]([CH2:46][NH2:47])[CH:41]=1>>[CH3:30][O:31][C:32]1[CH:39]=[CH:38][CH:37]=[CH:36][C:33]=1[CH2:34][NH:1][C:2]1[CH:11]=[C:10]([C:25]2[CH:24]=[CH:23][CH:22]=[CH:21][C:20]=2[CH3:15])[C:9]2[C:4](=[CH:5][CH:6]=[C:7]([NH:47][CH2:46][C:42]3[CH:41]=[N:40][CH:45]=[CH:44][CH:43]=3)[CH:8]=2)[N:3]=1参加物
5
実験手順
The title compound, MS: m/e=461.5 (M+H+), was prepared in accordance with the general method of example 30 from 2-amino-6-chloro-4-hydroxyquinoline (CAS 64319-84-2), o-tolyl-phenylboronic acid, 2-methoxybenzaldehyde and 3-picolylamine.
出典と根拠
- ORDレコード
- ord-1edd418d90594e94854fc7e41878e267
- 出典データセット
- uspto-grants-2013_03
- 特許番号
- US08399674B2
関連ノート
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