5-hydroxy-4-propyldihydrofuran-2(3H)-one → HCID 15979801、化合物
反応式
[F:1][C:2]1[CH:3]=[C:4]2[N:9]([C:10]=1[CH2:11][NH2:12])[CH:8]=[CH:7][CH:6]=[CH:5]2.O[CH:14]1[O:18][C:17](=O)[CH2:16][CH:15]1[CH2:20][CH2:21][CH3:22]>ClCCCl.ClCCl>[F:1][C:2]1[CH:3]=[C:4]2[N:9]([C:10]=1[CH2:11][N:12]1[CH2:14][CH:15]([CH2:20][CH2:21][CH3:22])[CH2:16][C:17]1=[O:18])[CH:8]=[CH:7][CH:6]=[CH:5]2参加物
実験手順
A solution of 1-(2-fluoroindolizin-3-yl)methanamine x263 (0.38 g, 2.3 mmol) and 5-hydroxy-4-propyldihydrofuran-2(3H)-one x252 (0.33 g, 2.3 mmol) in DCE (12 ml) is kept at room temperature for 2 h, then STAB (0.74 g, 3.5 mmol) is added, and the mixture is stirred overnight. The reaction mixture is kept under stirring at 50° C. for 2 h, cooled to room temperature, and diluted with dichloromethane (10 ml). The mixture is washed with a 20% K2CO3 solution (2×15 ml), and the aqueous layer is washed with brine (25 ml), dried over anhydrous Na2SO4 and evaporated. The residue (0.60 g) is purified by chromatography on silica gel (gradient: chloroform to chloroform/methanol 50/1) to isolate a product of approximately 80% purity (0.162 g). This product is purified by chromatography on silicagel (hexane/ethyl acetate 5/2) to afford pure 1-[(2-fluoroindolizin-3-yl)methyl]-4-propylpyrrolidin-2-one 264 (0.126 g).
後処理
- additionSTAB (0.74 g, 3.5 mmol) is added
- stirringunder stirring at 50° C. for 2 h
- washThe mixture is washed with a 20% K2CO3 solution (2×15 ml)
- washthe aqueous layer is washed with brine (25 ml)
- dry with materialdried over anhydrous Na2SO4
- customevaporated
- customThe residue (0.60 g) is purified by chromatography on silica gel (gradient: chloroform to chloroform/methanol 50/1)
- customto isolate a product of approximately 80% purity (0.162 g)
- customThis product is purified by chromatography on silicagel (hexane/ethyl acetate 5/2)
出典と根拠
- ORDレコード
- ord-545f5111903e4edfb863a7c0416c7ec9
- 出典データセット
- uspto-grants-2013_11
- 特許番号
- US08586623B2
反応ノート
読み込み中…