Ethyl Acrylate → 3-(7-bromo-2-oxo-2H-quinolin-1-yl)-propionic acid ethyl ester
反応式
[Br:1][C:2]1[CH:11]=[C:10]2[C:5]([CH:6]=[CH:7][C:8](=[O:12])[NH:9]2)=[CH:4][CH:3]=1.[C:13]([O:17][CH2:18][CH3:19])(=[O:16])[CH:14]=[CH2:15]>>[CH2:18]([O:17][C:13](=[O:16])[CH2:14][CH2:15][N:9]1[C:10]2[C:5](=[CH:4][CH:3]=[C:2]([Br:1])[CH:11]=2)[CH:6]=[CH:7][C:8]1=[O:12])[CH3:19]参加物
3
実験手順
The compound was obtained according to procedure H starting from 7-bromoquinolin-2(1H)-one (commercial; 561 mg, 2.5 mmol) and ethyl acrylate (0.27 mL, 2.5 mmol, 1 eq.). The crude orange oil (0.76 g; 94% yield) was used as such in the next step.
後処理
- customThe compound was obtained
出典と根拠
- ORDレコード
- ord-7b1c6348d79747fa8a461d16bfc9ffa5
- 出典データセット
- uspto-grants-2013_01
- 特許番号
- US08349826B2
反応ノート
読み込み中…