Propanoic acid, 2-bromo-2-methyl-, ethyl ester → 2-Methyl-2-[1,3-dimethyl-2-(4-pyridyl)-1H-indole-5-yloxy]-propanoic acid ethylester
反応式
[CH3:1][N:2]1[C:10]2[C:5](=[CH:6][C:7]([OH:11])=[CH:8][CH:9]=2)[C:4]([CH3:12])=[C:3]1[C:13]1[CH:18]=[CH:17][N:16]=[CH:15][CH:14]=1.[CH2:19]([O:21][C:22](=[O:27])[C:23](Br)([CH3:25])[CH3:24])[CH3:20]>>[CH2:19]([O:21][C:22](=[O:27])[C:23]([CH3:25])([O:11][C:7]1[CH:6]=[C:5]2[C:10](=[CH:9][CH:8]=1)[N:2]([CH3:1])[C:3]([C:13]1[CH:18]=[CH:17][N:16]=[CH:15][CH:14]=1)=[C:4]2[CH3:12])[CH3:24])[CH3:20]参加物
3
実験手順
The above compound was prepared from 1,3-dimethyl-2-(4-pyridyl)-1H-indole-5-ol and 2-bromo-2-methyl-propanoic acid ethylester using a procedure analogous to that of Example 10.
出典と根拠
- ORDレコード
- ord-8c0c703b46db48e8b1912f4af97ac928
- 出典データセット
- uspto-grants-1982_08
- 特許番号
- US04343811
反応ノート
読み込み中…