Potassium Iodide → 6-Ketonalbuphine

HRID 39326

反応式

HRID 39326 の反応式
[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

6

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

  1. stirringThe reaction was stirred for an additional 7 days
  2. customwas consumed
  3. additionDistilled water (50 mL) was added
  4. stirringstirred at room temperature for 6 hours
  5. customAn off-white precipitate formed
  6. customwhich was removed by filtration
  7. washThe solid was washed with distilled water (25 mL)
  8. waitslurried for 24 hours in acetonitrile (25 mL)
  9. filtrationFiltration
  10. washwashing the solid with acetonitrile (10 mL)
  11. 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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