N-allyl-5-azaisatin → 1H-Pyrrolo[3,2-c]pyridine-2,3-dione
反応式
C([N:4]1[C:14]2[C:9](=[CH:10][N:11]=[CH:12][CH:13]=2)[C:7](=[O:8])[C:5]1=[O:6])C=C>C1(C)C=CC=CC=1>[NH:4]1[C:14]2[C:9](=[CH:10][N:11]=[CH:12][CH:13]=2)[C:7](=[O:8])[C:5]1=[O:6]参加物
3
実験手順
A solution of N-allyl-5-azaisatin (5.3 mmol), (Ph3P)3RhCl (0.5 mmol) in aqueous toluene is stirred under a nitrogen atmosphere at room temperature overnight. The organic layer is dried (MgSO4) and the solvent is evaporated. The residue is stirred in 1N HCl/MeOH for 15 min after which time the methanol is evaporated and the pH of the water is adjusted to 7. A precipitate is formed and purified by silica gel chromatography (1% MeOH:CHCl3) to obtain the title compound.
後処理
- dry with materialThe organic layer is dried (MgSO4)
- customthe solvent is evaporated
- customis evaporated
- customA precipitate is formed
- custompurified by silica gel chromatography (1% MeOH:CHCl3)
出典と根拠
- ORDレコード
- ord-13e4f4d258794ec5a2973b4328ee72fb
- 出典データセット
- uspto-grants-1995_08
- 特許番号
- US05441955
反応ノート
読み込み中…