Oxalic Acid → 2-(1-Trityl-1h-imidazol-4-yl)-benzylamine oxalate salt
反応式
[C:1]([N:20]1[CH:24]=[C:23]([C:25]2[CH:32]=[CH:31][CH:30]=[CH:29][C:26]=2[CH2:27][NH2:28])[N:22]=[CH:21]1)([C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1)([C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[C:33]([OH:38])(=[O:37])[C:34]([OH:36])=[O:35].CCCCCC>O1CCCC1>[C:33]([OH:38])(=[O:37])[C:34]([OH:36])=[O:35].[C:1]([N:20]1[CH:24]=[C:23]([C:25]2[CH:32]=[CH:31][CH:30]=[CH:29][C:26]=2[CH2:27][NH2:28])[N:22]=[CH:21]1)([C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1)([C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1)[C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1参加物
5
実験手順
The crude 2-(1-trityl-1H-imidazol-4-yl)-benzylamine (66.1 g, 159 mmol) was dissolved in tetrahydrofuran (420 ml). Solid oxalic acid (14.3 g, 159 mmol) was added to the solution while stirring. This mixture was stirred at room temperature for 15 min and then added dropwise to stirring hexane (2000 ml). Tetrahydrofuran (100 ml) was used to rinse the glassware. A yellow solid precipitated. The mixture was stirred for an additional 20 min and the product was isolated by filtration. The solid was rinsed with 4:1 hexane:tetrahydrofuran (625 ml) and dried in a vacuum oven at ˜45° C. with an air purge for 18 h to afford 2-(1-trityl-1H-imidazol-4-yl)-benzylamine oxalate salt; MS (ES+) M+1 416.6 for C29H25N3.
後処理
- stirringThis mixture was stirred at room temperature for 15 min
- additionadded dropwise
- washto rinse the glassware
- customA yellow solid precipitated
- stirringThe mixture was stirred for an additional 20 min
- customthe product was isolated by filtration
- washThe solid was rinsed with 4:1 hexane
- dry with materialtetrahydrofuran (625 ml) and dried in a vacuum oven at ˜45° C. with an air
- custompurge for 18 h
出典と根拠
- ORDレコード
- ord-abcb3b73f49b44449652b1098bdef782
- 出典データセット
- uspto-grants-2006_04
- 特許番号
- US07026324B2
反応ノート
読み込み中…