Water → 3-bromo-1-isopropyl-1H-pyrazolo[4,3-b]pyridine
反応式
[Br:1][C:2]1[C:6]2=[N:7][CH:8]=[CH:9][CH:10]=[C:5]2[NH:4][N:3]=1.I[CH:12]([CH3:14])[CH3:13].C([O-])([O-])=O.[K+].[K+].O>CN(C=O)C>[Br:1][C:2]1[C:6]2=[N:7][CH:8]=[CH:9][CH:10]=[C:5]2[N:4]([CH:12]([CH3:14])[CH3:13])[N:3]=1参加物
6
実験手順
To a solution of 3-bromo-1H-pyrazolo[4,3-b]pyridine (200 mg) in DMF (10 mL) were added 2-iodopropane (0.20 mL) and K2CO3 (168 mg) at room temperature. After stirring overnight, the reaction mixture was poured into water and extracted with AcOEt. The extract was washed with water and brine, dried over MgSO4, and concentrated under reduced pressure. The residue was purified by basic silica gel column chromatography (AcOEt/hexane) to give the title compound (147 mg).
後処理
- extractionextracted with AcOEt
- washThe extract was washed with water and brine
- dry with materialdried over MgSO4
- concentrationconcentrated under reduced pressure
- customThe residue was purified by basic silica gel column chromatography (AcOEt/hexane)
出典と根拠
- ORDレコード
- ord-aaa3de8565e3451387055b3d63cba6ea
- 出典データセット
- uspto-grants-2015_05
- 特許番号
- US09029536B2
反応ノート
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