Iodine → (6R*,9aS*)-6-(3-fluorophenyl)-3-iodooctahydroquinolizin-4-one
反応式
I[Si](C)(C)C.[F:6][C:7]1[CH:8]=[C:9]([C@H:13]2[CH2:22][CH2:21][CH2:20][C@@H:19]3[N:14]2[C:15](=[O:23])[CH2:16][CH2:17][CH2:18]3)[CH:10]=[CH:11][CH:12]=1.CN(C)CCN(C)C.[I:32]I.S([O-])([O-])(=O)=S.[Na+].[Na+]>C(Cl)Cl.C(OCC)(=O)C>[F:6][C:7]1[CH:8]=[C:9]([C@H:13]2[CH2:22][CH2:21][CH2:20][C@@H:19]3[N:14]2[C:15](=[O:23])[CH:16]([I:32])[CH2:17][CH2:18]3)[CH:10]=[CH:11][CH:12]=1参加物
反応物 5
生成物 1
試薬・触媒・溶媒 2
実験手順
Iodotrimethylsilane (0.34 mL) was added to a solution of (6R*,9aS*)-6-(3-fluorophenyl) octahydroquinolizin-4-one (383 mg) and N,N,N′,N′-tetramethylethylenediamine (0.82 mL) in methylene chloride (15 mL) under ice-cooling in a nitrogen atmosphere, and the reaction solution was stirred under ice-cooling for 30 minutes. Iodine (590 mg) was added to the reaction solution under ice-cooling, and the reaction solution was stirred under ice-cooling for one hour. Ethyl acetate and a saturated sodium thiosulfate solution were added to the reaction solution, and the organic layer was separated. The resulting organic layer was washed with brine, dried over magnesium sulfate, and then concentrated under reduced pressure to obtain 597 mg of the title compound. The property value of the compound is as follows.
後処理
- temperaturecooling in a nitrogen atmosphere
- temperaturecooling for 30 minutes
- temperaturecooling
- stirringthe reaction solution was stirred under ice-
- temperaturecooling for one hour
- customthe organic layer was separated
- washThe resulting organic layer was washed with brine
- dry with materialdried over magnesium sulfate
- concentrationconcentrated under reduced pressure
出典と根拠
- ORDレコード
- ord-ad84cbae4c9a420282e4f6bafe4bb616
- 出典データセット
- uspto-grants-2011_11
- 特許番号
- US08048878B2
反応ノート
読み込み中…