N-Methoxy-N-methylpropionamide → 1-(2-((tert-Butyldimethylsilyloxy)methyl)-1-methyl-1H-indol-5-yl)propan-1-one
反応式
Br[C:2]1[CH:3]=[C:4]2[C:8](=[CH:9][CH:10]=1)[N:7]([CH3:11])[C:6]([CH2:12][O:13][Si:14]([C:17]([CH3:20])([CH3:19])[CH3:18])([CH3:16])[CH3:15])=[CH:5]2.[Li]CCCC.CON(C)[C:29](=[O:32])[CH2:30][CH3:31]>C1COCC1>[Si:14]([O:13][CH2:12][C:6]1[N:7]([CH3:11])[C:8]2[C:4]([CH:5]=1)=[CH:3][C:2]([C:29](=[O:32])[CH2:30][CH3:31])=[CH:10][CH:9]=2)([C:17]([CH3:20])([CH3:19])[CH3:18])([CH3:16])[CH3:15]参加物
反応条件
- 温度
- -78 °C
実験手順
To a stirred solution of 5-bromo-2-((tert-butyldimethylsilyloxy)methyl)-1-methyl-1H-indole (3.76 g, 10.6 mmol), prepared according to procedure described in Example 39 Step 3, in THF (15 mL) was added n-BuLi (2.5 M solution in hexanes, 5.1 mL, 12.7 mmol, 1.2 eq) at −78° C. dropwise. The mixture was stirred for 30 min at −78° C. before a solution of N-methoxy-N-methylpropionamide (1.49 g, 12.7 mmol, 1.2 eq) in THF (5 mL) was added. After stirred at −78° C. for 10 min, the reaction was quenched with saturated aqueous NH4Cl solution. The resulting mixture was extracted by ether (3×30 mL) and combined organic layers were dried over Na2SO4. The crude product was purified by flash chromatography (0-10% EtOAc in hexanes) to give the title compound (2.70 g, 77%).
後処理
- additionwas added
- customthe reaction was quenched with saturated aqueous NH4Cl solution
- extractionThe resulting mixture was extracted by ether (3×30 mL)
- dry with materialwere dried over Na2SO4
- customThe crude product was purified by flash chromatography (0-10% EtOAc in hexanes)
出典と根拠
- ORDレコード
- ord-d2140aa71d614955934064ad5a25c1b4
- 出典データセット
- uspto-grants-2016_08
- 特許番号
- US09409905B2
反応ノート
読み込み中…