Triethylamine → [[2-[(4-Methylpiperazinyl)carbonyl]phenyl]methoxy]-N-octadecylformamide
反応式
C(N(CC)CC)C.[CH2:8]([N:26]=[C:27]=[O:28])[CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH3:25].[CH3:29][N:30]1[CH2:35][CH2:34][N:33]([C:36]([C:38]2[CH:43]=[CH:42][CH:41]=[CH:40][C:39]=2[CH2:44][OH:45])=[O:37])[CH2:32][CH2:31]1>ClCCl>[CH3:29][N:30]1[CH2:31][CH2:32][N:33]([C:36]([C:38]2[CH:43]=[CH:42][CH:41]=[CH:40][C:39]=2[CH2:44][O:45][N:26]([CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH3:25])[CH:27]=[O:28])=[O:37])[CH2:34][CH2:35]1参加物
5
実験手順
Triethylamine (6.50 ml) and octadecyl isocyanate (14.40 ml) were added to a solution of the syrup containing 2-(hydroxymethyl)phenyl 4-methylpiperazinyl ketone (9.83 g) in dichloromethane (100 ml). After being stirred for 14.5 hours at room temperature, the insoluble material was filtrated out under a vacuum. The filtrate was concentrated. The residue was purified by silica gel column chromatography (silica gel 225 g, chloroform:methanol=80:1), thereby yielding 12.00 g of the aimed compound as white solid.
後処理
- filtrationthe insoluble material was filtrated out under a vacuum
- concentrationThe filtrate was concentrated
- customThe residue was purified by silica gel column chromatography (silica gel 225 g, chloroform:methanol=80:1)
出典と根拠
- ORDレコード
- ord-6a2a5ca01348482ca2ba2778a554984b
- 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…