Sodium Azide → 2-Pyrrolidinone, 5-(azidomethyl)-, (5S)-
反応式
[O:1]=[C:2]1[NH:6][C@H:5]([CH2:7]OS(C2C=CC(C)=CC=2)(=O)=O)[CH2:4][CH2:3]1.[N-:19]=[N+:20]=[N-:21].[Na+]>CN(C=O)C>[N:19]([CH2:7][C@H:5]1[NH:6][C:2](=[O:1])[CH2:3][CH2:4]1)=[N+:20]=[N-:21]参加物
4
反応条件
- 温度
- 55 °C
実験手順
A round bottom flask was charged with (S)-(5-oxopyrrolidin-2-yl)methyl-4-methylbenzenesulfonate (18.4 g, 68.5 mmol), DMF (400 mL), and NaN3 (17.8 g, 274 mmol). The resulting mixture was stirred at 55° C. for overnight. Removal of solvent under reduced pressure followed by flash chromatography purification (7% MeOH in CHCl3 as the eluent) provided the (S)-5-(azidomethyl) pyrrolidin-2-one (8.45 g, 60.36 mmol, 88%) as a yellow oil.
後処理
- customRemoval of solvent under reduced pressure
- customfollowed by flash chromatography purification (7% MeOH in CHCl3 as the eluent)
出典と根拠
- ORDレコード
- ord-cfa990570e664226b90a6c90b3034ebc
- 出典データセット
- uspto-grants-2016_09
- 特許番号
- US09446393B2
反応ノート
読み込み中…