Methyl iodide → ethyl 7-methoxy-1-(tetrahydro-2H-pyran-2-yl)-1H-indazole-5-carboxylate
反応式
[OH:1][C:2]1[CH:3]=[C:4]([C:17]([O:19][CH2:20][CH3:21])=[O:18])[CH:5]=[C:6]2[C:10]=1[N:9]([CH:11]1[CH2:16][CH2:15][CH2:14][CH2:13][O:12]1)[N:8]=[CH:7]2.[C:22]([O-])([O-])=O.[K+].[K+].IC>CC(C)=O>[CH3:22][O:1][C:2]1[CH:3]=[C:4]([C:17]([O:19][CH2:20][CH3:21])=[O:18])[CH:5]=[C:6]2[C:10]=1[N:9]([CH:11]1[CH2:16][CH2:15][CH2:14][CH2:13][O:12]1)[N:8]=[CH:7]2参加物
実験手順
To a solution of ethyl 7-hydroxy-1-(tetrahydro-2H-pyran-2-yl)-1H-indazole-5-carboxylate (1.45 g, 5.0 mmol) in acetone (20 mL) containing K2CO3 (760 mg, 5.50 mmol) was added iodomethane (781 mg, 0.34 mL, 5.5 mmo). The mixture was heated at reflux under N2 overnight. The mixture was cooled to room temperature, filtered, evaporated and partitioned between EtOAc and water. The aqueous phase was extracted with additional EtOAc. The combined organic extracts were washed with saturated aqueous NaCl, dried over Na2SO4, filtered and concentrated to provide crude product. The crude material was purified by chromatography (Isco, 0-40% EtOAc/heptane) to provide material which was dried under high vacuum overnight to afford ethyl 7-methoxy-1-(tetrahydro-2H-pyran-2-yl)-1H-indazole-5-carboxylate (1.40 g, 92%).
後処理
- temperatureThe mixture was heated
- temperatureat reflux under N2 overnight
- filtrationfiltered
- customevaporated
- custompartitioned between EtOAc and water
- extractionThe aqueous phase was extracted with additional EtOAc
- washThe combined organic extracts were washed with saturated aqueous NaCl
- dry with materialdried over Na2SO4
- filtrationfiltered
- concentrationconcentrated
- customto provide crude product
- customThe crude material was purified by chromatography (Isco, 0-40% EtOAc/heptane)
- customto provide material which
- customwas dried under high vacuum overnight
出典と根拠
- ORDレコード
- ord-be8145f0082545c3a098be7ec0e1471c
- 出典データセット
- uspto-grants-2012_11
- 特許番号
- US08318762B2
反応ノート
読み込み中…