Diallylamine → 2-[3-(4-Chlorophenyl)-1,2-dimethyl-1H-indole-5-yloxy]-2-methyl-propanoic acid-diallylamide
反応式
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[C:16]3[C:11](=[CH:12][CH:13]=[C:14]([O:17][C:18]([CH3:23])([CH3:22])[C:19]([OH:21])=O)[CH:15]=3)[N:10]([CH3:24])[C:9]=2[CH3:25])=[CH:4][CH:3]=1.[CH2:26]([NH:29][CH2:30][CH:31]=[CH2:32])[CH:27]=[CH2:28]>>[CH2:26]([N:29]([CH2:30][CH:31]=[CH2:32])[C:19](=[O:21])[C:18]([O:17][C:14]1[CH:15]=[C:16]2[C:11](=[CH:12][CH:13]=1)[N:10]([CH3:24])[C:9]([CH3:25])=[C:8]2[C:5]1[CH:4]=[CH:3][C:2]([Cl:1])=[CH:7][CH:6]=1)([CH3:22])[CH3:23])[CH:27]=[CH2:28]参加物
3
実験手順
The above compound was prepared from 2-[3-(4-chlorophenyl)-1,2-dimethyl-1H-indole-5-yloxy]-2-methyl-propanoic acid and diallylamine using a procedure analogous to that of Example 130.
出典と根拠
- ORDレコード
- ord-303ad3515a614e0bbe59cb49a6829144
- 出典データセット
- uspto-grants-1982_08