Sodium borohydride → 4-FLUORO-N-[5-(1-HYDROXY-ETHYL)-INDAN-2-yl]-BENZAMIDE
反応式
[C:1]([C:4]1[CH:5]=[C:6]2[C:10](=[CH:11][CH:12]=1)[CH2:9][CH:8]([NH:13][C:14](=[O:22])[C:15]1[CH:20]=[CH:19][C:18]([F:21])=[CH:17][CH:16]=1)[CH2:7]2)(=[O:3])[CH3:2].[BH4-].[Na+]>CO>[F:21][C:18]1[CH:17]=[CH:16][C:15]([C:14]([NH:13][CH:8]2[CH2:7][C:6]3[C:10](=[CH:11][CH:12]=[C:4]([CH:1]([OH:3])[CH3:2])[CH:5]=3)[CH2:9]2)=[O:22])=[CH:20][CH:19]=1参加物
4
実験手順
400 mg (1.35 mmol) N-(5-acetyl-indan-2-yl)-4-fluoro-benzamide were dissolved in 10 ml of methanol, then 100 mg (2.7 mmol) sodium borohydride were added. The mixture was worked up by dropping onto ice/HCl, the resulting solid was filtered off.
後処理
- filtrationthe resulting solid was filtered off
出典と根拠
- ORDレコード
- ord-51d7265b3dcf4f578852d6ad6333a988
- 出典データセット
- uspto-grants-2012_04
- 特許番号
- US08163751B2
反応ノート
読み込み中…