反応式
[Br:1][C:2]1[CH:7]=[CH:6][C:5]2[C:8]3([CH2:18][O:19][C:4]=2[CH:3]=1)[C:16]1[C:11](=[CH:12][CH:13]=[CH:14][CH:15]=1)[NH:10][C:9]3=[O:17].C(=O)([O-])[O-].[Cs+].[Cs+].CC1C=CC(S(O[CH2:37][C@H:38]2[CH2:42][CH2:41][CH2:40][O:39]2)(=O)=O)=CC=1>CC(=O)CC>[Br:1][C:2]1[CH:7]=[CH:6][C:5]2[C:8]3([CH2:18][O:19][C:4]=2[CH:3]=1)[C:16]1[C:11](=[CH:12][CH:13]=[CH:14][CH:15]=1)[N:10]([CH2:37][C@H:38]1[CH2:42][CH2:41][CH2:40][O:39]1)[C:9]3=[O:17]参加物
5
反応物 3
生成物 1
試薬・触媒・溶媒 1
実験手順
To a stirred solution of 6-bromospiro[1-benzofuran-3,3′-indol]-2′(1′H)-one (1.3 g, 4.3 mmol) in 2-butanone (40.0 mL) was added cesium carbonate (4.2 g, 12.9 mmol) and (R)-(tetrahydrofuran-2-yl)methyl 4-methylbenzenesulfonate (1.4 g, 5.4 mmol). The reaction was refluxed for 16 h, filtered and concentrated in vacuo to dryness. The residue was purified by flash chromatography with 25% ethyl acetate in hexanes to afford 6-bromo-1′-[(2R)-tetrahydrofuran-2-ylmethyl]spiro[1-benzofuran-3,3′-indol]-2′(1′H)-one (1.75 g, 100%) as a colorless solid: MS (ES+) m/z 400.0 (M+1), 402.0 (M+1).
後処理
- temperatureThe reaction was refluxed for 16 h
- filtrationfiltered
- concentrationconcentrated in vacuo to dryness
- customThe residue was purified by flash chromatography with 25% ethyl acetate in hexanes
出典と根拠
- ORDレコード
- ord-9a7ffba37537471f93292c4d2011ebb5
- 出典データセット
- uspto-grants-2012_01
- 特許番号
- US08101647B2
関連ノート
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