1-(4-Amino-2-methylquinolin-3-yl)ethanone → HCID 12019318、化合物
反応式
[Br:1][C:2]1[CH:23]=[CH:22][C:5]([CH2:6][NH:7][C:8]2[C:17]3[C:12](=[CH:13][CH:14]=[CH:15][CH:16]=3)[N:11]=[C:10]([CH3:18])[C:9]=2[C:19](=[O:21])[CH3:20])=[CH:4][CH:3]=1.NC1C2C(=CC=CC=2)N=C(C)C=1C(=O)C.BrC1C=CC(CBr)=CC=1[Cl:48]>>[Br:1][C:2]1[CH:3]=[CH:4][C:5]([CH2:6][NH:7][C:8]2[C:17]3[C:12](=[CH:13][CH:14]=[CH:15][CH:16]=3)[N:11]=[C:10]([CH3:18])[C:9]=2[C:19](=[O:21])[CH3:20])=[CH:22][C:23]=1[Cl:48]参加物
4
実験手順
1-(4-(4-Bromo-3-chlorobenzylamino)-2-methylquinolin-3-yl)ethanone was synthesized by the same process as described for 1-(4-(4-bromobenzylamino)-2-methylquinolin-3-yl)ethanone (Example 1, Intermediate 2c) starting from 1-(4-amino-2-methylquinolin-3-yl)ethanone and 4-bromo-3-chlorobenzyl bromide. MS(ES+):403/405.
出典と根拠
- ORDレコード
- ord-b9ad399c344d4b478156e248ebd96c88
- 出典データセット
- uspto-grants-2002_01
- 特許番号
- US06339077B1
反応ノート
読み込み中…