Tetrabutylammonium Fluoride → methyl 1H-pyrrolo[2,3-b]pyridine-5-carboxylate
反応式
[CH3:1][O:2][C:3]([C:5]1[CH:6]=[C:7]2[CH:13]=[CH:12][N:11]([Si](C(C)C)(C(C)C)C(C)C)[C:8]2=[N:9][CH:10]=1)=[O:4].[F-].C([N+](CCCC)(CCCC)CCCC)CCC>O1CCCC1>[CH3:1][O:2][C:3]([C:5]1[CH:6]=[C:7]2[CH:13]=[CH:12][NH:11][C:8]2=[N:9][CH:10]=1)=[O:4]参加物
4
実験手順
To 1-Triisopropylsilanyl-1H-pyrrolo[2,3-b]pyridine-5-carboxylic acid methyl ester (531, 0.950 g, 2.9 mmol) in tetrahydrofuran (20.0 mL) was added tetrabutyl-ammonium fluoride, trihydrate (1.20 g, 3.8 mmol). The reaction was stirred at room temperature for 10 minutes. The reaction was concentrated and purified with silica gel column chromatography eluting with 4% methanol in methylene chloride to give the compound as a white solid (532, 300 mg, 60%). MS (ESI) [M+H+]+=177.2.
後処理
- concentrationThe reaction was concentrated
- custompurified with silica gel column chromatography
- washeluting with 4% methanol in methylene chloride
出典と根拠
- ORDレコード
- ord-ba47cbfcf8584a0fb570d4a643681d56
- 出典データセット
- uspto-grants-2012_03
- 特許番号
- US08143271B2
反応ノート
読み込み中…