4-(1H-Indol-3-YL)cyclohexanone → 4-[4-(2-Methoxy-phenyl)-piperazin-1-yl]-cyclohexanone
反応式
N1C2C(=CC=CC=2)C(C2CCC(=O)CC2)=C1.[CH3:17][O:18][C:19]1[CH:24]=[CH:23][CH:22]=[CH:21][C:20]=1[N:25]1[CH2:30][CH2:29][N:28]([CH:31]2[CH2:40][CH2:39][C:34]3(OCC[O:35]3)[CH2:33][CH2:32]2)[CH2:27][CH2:26]1>>[CH3:17][O:18][C:19]1[CH:24]=[CH:23][CH:22]=[CH:21][C:20]=1[N:25]1[CH2:30][CH2:29][N:28]([CH:31]2[CH2:40][CH2:39][C:34](=[O:35])[CH2:33][CH2:32]2)[CH2:27][CH2:26]1参加物
3
実験手順
This compound was prepared in the manner described above for intermediate 3a by replacing 3-(o 1,4-dioxa-spiro[4,5]dec-8-yl)1H-indole with 1-(2-methoxy-phenyl)4-(1,4-dioxa-spiro[4,5]dec-8-yl)-piperazine (5.0 g, 15 mmol) to afford 4.0 g (93%) of the title compound.
後処理
- customThis compound was prepared in the manner
出典と根拠
- ORDレコード
- ord-e9bb3fd0abd3420387128a7a67907cf9
- 出典データセット
- uspto-grants-2002_10
- 特許番号
- US06465482B2
反応ノート
読み込み中…