反応式
[C:1]1([S:7]([N:10]2[C:14]3=[N:15][CH:16]=[C:17]([F:19])[CH:18]=[C:13]3[CH:12]=[CH:11]2)(=[O:9])=[O:8])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[CH2:20]([Li])[CH2:21][CH2:22][CH3:23].[CH3:25][CH2:26][CH2:27]CCC.C1(C=[O:37])CCCC1>O1CCCC1>[C:1]1([S:7]([N:10]2[C:14]3=[N:15][CH:16]=[C:17]([F:19])[CH:18]=[C:13]3[CH:12]=[C:11]2[CH:20]([OH:37])[CH2:21][CH:22]2[CH2:23][CH2:27][CH2:26][CH2:25]2)(=[O:9])=[O:8])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1参加物
反応条件
- 温度
- -78 °C
実験手順
To a suspension of 1-benzenesulfonyl-5-fluoro-1H-pyrrolo[2,3-b]pyridine (2.0 g, 7.25 mmol) in dry tetrahydrofuran (150 mL) at −78° C. was added a solution of n-butyllithium in n-hexane (1.6 M, 6.8 mL, 10.9 mmol) dropwise. The mixture was stirred at −78° C. for 30 min and then treated with cyclopentanecarbaldehyde (1.5 g, 13.04 mmol) dropwise. The resulting mixture was stirred at −78° C. for 1 h and quenched with brine. The mixture was extracted with ethyl acetate (2×100 mL), washed with brine, dried over anhydrous sodium sulfate and concentrated in vacuo. Purification by flash column chromatography (QingDao silica gel, 200-300 mesh, 15% ethyl acetate/hexanes) afforded 1-(1-benzenesulfonyl-5-fluoro-1H-pyrrolo[2,3-b]pyridin-2-yl)-2-cyclopentyl-ethanol as a colorless oil (2.1 g, 74%): LC/MS m/e calcd for C20H21FN2O3S [M+H]+ 389.46, observed 389.0.
後処理
- stirringThe resulting mixture was stirred at −78° C. for 1 h
- customquenched with brine
- extractionThe mixture was extracted with ethyl acetate (2×100 mL)
- washwashed with brine
- dry with materialdried over anhydrous sodium sulfate
- concentrationconcentrated in vacuo
- customPurification by flash column chromatography (QingDao silica gel, 200-300 mesh, 15% ethyl acetate/hexanes)
出典と根拠
- ORDレコード
- ord-12e6c0f53c6f49128d6fa6cda1f7dc56
- 出典データセット
- uspto-grants-2012_07
- 特許番号
- US08222416B2
関連ノート
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