Hydrochloric Acid → HCID 86755725、化合物
反応式
[ClH:1].[CH3:2][N:3]1[CH2:8][CH2:7][N:6]([C:9]([C:11]2[CH:16]=[CH:15][CH:14]=[CH:13][C:12]=2[CH2:17][O:18][N:19]([CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH2:31][CH2:32][CH2:33][CH2:34][CH2:35][CH2:36][CH2:37][CH2:38][CH3:39])[CH:20]=[O:21])=[O:10])[CH2:5][CH2:4]1>C(OCC)(=O)C>[ClH:1].[CH3:2][N:3]1[CH2:4][CH2:5][N:6]([C:9]([C:11]2[CH:16]=[CH:15][CH:14]=[CH:13][C:12]=2[CH2:17][O:18][N:19]([CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH2:31][CH2:32][CH2:33][CH2:34][CH2:35][CH2:36][CH2:37][CH2:38][CH3:39])[CH:20]=[O:21])=[O:10])[CH2:7][CH2:8]1参加物
4
実験手順
4N Hydrochloric acid--ethyl acetate solution (8.50 ml) was added to a solution of [[2-[(4-methylpiperazinyl)carbonyl]phenyl]methoxy]-N-octadecylformamide (11.98 g) in ethyl acetate (120 ml) while being cooled with ice. After being stirred for 30 minutes at room temperature, the reaction mixture was concentrated. The residue was recrystallized from ethyl acetate-ethanol mixed solvent, thereby yielding 12.12 g of the aimed compound as white solid.
後処理
- temperaturewhile being cooled with ice
- concentrationthe reaction mixture was concentrated
- customThe residue was recrystallized from ethyl acetate-ethanol mixed solvent
出典と根拠
- ORDレコード
- ord-98ab8e0292ac4e08a1c2e69868fc2a70
- 出典データセット
- uspto-grants-2000_09
- 特許番号
- US06114325
反応ノート
読み込み中…