反応式
[CH3:1][N:2]1[C@@H:12]2[CH2:13][C:14]3[CH:19]=[CH:18][C:17]([OH:20])=[C:16]4[O:21][C@H:6]5[C:7]([CH:9]=[CH:10][C@:11]2([OH:22])[C@:5]5([C:15]=34)[CH2:4][CH2:3]1)=[O:8].C(=O)([O-])[O-].[K+].[K+].[I-].[K+].BrC[CH:33]1[CH2:36][CH2:35][CH2:34]1>CC(N(C)C)=O>[CH2:33]1[CH2:36][CH:35]([CH2:1][N:2]2[C@@H:12]3[CH2:13][C:14]4[CH:19]=[CH:18][C:17]([OH:20])=[C:16]5[O:21][C@H:6]6[C:7]([CH2:9][CH2:10][C@:11]3([OH:22])[C@:5]6([C:15]=45)[CH2:4][CH2:3]2)=[O:8])[CH2:34]1参加物
実験手順
Noroxymorphone (1.59 g, 5.5 mmol), potassium carbonate (0.61 g, 6.1 mmol), potassium iodide (0.46 g, 2.8 mmol), and dimethyl acetamide (10 mL) were added into a round bottom flask. Bromomethylcyclobutane (0.82 g, 5.5 mmol, 0.62 mL) was added. The reaction was stirred for 7 days at room temperature. At that time, bromomethylcyclobutane (0.82 g, 5.5 mmol, 0.62 mL) was added. The reaction was stirred for an additional 7 days. HPLC analysis indicated that the noroxymorphone was consumed. Distilled water (50 mL) was added and stirred at room temperature for 6 hours. An off-white precipitate formed, which was removed by filtration. The solid was washed with distilled water (25 mL), then slurried for 24 hours in acetonitrile (25 mL). Filtration, washing the solid with acetonitrile (10 mL), and drying at room temperature under vacuum for 24 hours yielded N-(cyclobutylmethyl)-noroxymorphone (1.43 g, 73% yield) as a tan solid.
後処理
- stirringThe reaction was stirred for an additional 7 days
- customwas consumed
- additionDistilled water (50 mL) was added
- stirringstirred at room temperature for 6 hours
- customAn off-white precipitate formed
- customwhich was removed by filtration
- washThe solid was washed with distilled water (25 mL)
- waitslurried for 24 hours in acetonitrile (25 mL)
- filtrationFiltration
- washwashing the solid with acetonitrile (10 mL)
- customdrying at room temperature under vacuum for 24 hours
出典と根拠
- ORDレコード
- ord-51eb604ae3e04854819ac25796e786bd
- 出典データセット
- uspto-grants-2013_09
- 特許番号
- US08524904B2
関連ノート
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