Sodium Azide → (Methylethoxycarbonyloxy)methyl (2R)-4-[(3-azidopropyl)sulfonyloxy]-3,3-dimethyl-2-(phenylmethoxy)butanoate
反応式
Cl[CH2:2][CH2:3][CH2:4][S:5]([O:8][CH2:9][C:10]([CH3:32])([CH3:31])[C@@H:11]([O:23][CH2:24][C:25]1[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=1)[C:12]([O:14][CH2:15][O:16][C:17]([O:19][CH:20]([CH3:22])[CH3:21])=[O:18])=[O:13])(=[O:7])=[O:6].[N-:33]=[N+:34]=[N-:35].[Na+]>CS(C)=O>[N:33]([CH2:2][CH2:3][CH2:4][S:5]([O:8][CH2:9][C:10]([CH3:32])([CH3:31])[C@@H:11]([O:23][CH2:24][C:25]1[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=1)[C:12]([O:14][CH2:15][O:16][C:17]([O:19][CH:20]([CH3:22])[CH3:21])=[O:18])=[O:13])(=[O:7])=[O:6])=[N+:34]=[N-:35]参加物
4
反応物 2
生成物 1
試薬・触媒・溶媒 1
実験手順
Following the general procedure for the preparation of azides of Description 16, (methylethoxycarbonyloxy)methyl (2R)-4-[(3-chloropropyl)sulfonyloxy]-3,3-dimethyl-2-(phenylmethoxy)butanoate (27a) (0.14 g, 0.28 mmol) dissolved in 3 mL of anhydrous dimethyl sulfoxide (DMSO) was reacted with 45 mg (0.7 mmol) of sodium azide (NaN3). After work-up, the crude title compound (27) was used in the next step without further purification. MS (ESI) m/z 524.06 (M+Na)+.
後処理
- customAfter work-up, the crude title compound (27) was used in the next step without further purification
出典と根拠
- ORDレコード
- ord-bebf569e23554b4aa753855bb6c94dd3
- 出典データセット
- uspto-grants-2012_05
- 特許番号
- US08168617B2
反応ノート
読み込み中…