Cesium carbonate → 3-Hydroxy-2-methyl-3-[4-(2-methyl-quinolin-4-ylmethoxy)-phenyl]-propionic acid methyl ester
反応式
[CH3:1][O:2][C:3](=[O:15])[CH:4]([CH3:14])[CH:5]([OH:13])[C:6]1[CH:11]=[CH:10][C:9]([OH:12])=[CH:8][CH:7]=1.Cl[CH2:17][C:18]1[C:27]2[C:22](=[CH:23][CH:24]=[CH:25][CH:26]=2)[N:21]=[C:20]([CH3:28])[CH:19]=1.C(=O)([O-])[O-].[Cs+].[Cs+]>CS(C)=O>[CH3:1][O:2][C:3](=[O:15])[CH:4]([CH3:14])[CH:5]([OH:13])[C:6]1[CH:11]=[CH:10][C:9]([O:12][CH2:17][C:18]2[C:27]3[C:22](=[CH:23][CH:24]=[CH:25][CH:26]=3)[N:21]=[C:20]([CH3:28])[CH:19]=2)=[CH:8][CH:7]=1参加物
反応物 3
生成物 1
試薬・触媒・溶媒 1
実験手順
The 3-hydroxy-3-(4-hydroxy-phenyl)-2-methyl-propionic acid methyl ester (0.24 g, 1.14 mmol) was combined with the 4-chloromethyl-2-methyl-quinoline (0.313 g, 1.37 mmol) and cesium carbonate (1.1 g, 3.42 mmol) in DMSO (5 mL) at room temperature under a nitrogen atmosphere. The reaction was stirred for 18 h, filtered to remove the solids, and then partitioned between ethyl acetate and water. The organic layer was washed with brine, dried over magnesium sulfate, and concentrated to give a mixture of diasteromers. The product was purified by FCC on silica gel eluting with ethyl acetate:hexane (60:40, v: v) to give 3-hydroxy-2-methyl-3-[4-(2-methyl-quinolin-4-ylmethoxy)-phenyl]-propionic acid methyl ester (0.352 g, 84%) as a glass. MS found: (M+H)+=366.
後処理
- filtrationfiltered
- customto remove the solids
- custompartitioned between ethyl acetate and water
- washThe organic layer was washed with brine
- dry with materialdried over magnesium sulfate
- concentrationconcentrated
- customto give
- additiona mixture of diasteromers
- customThe product was purified by FCC on silica gel eluting with ethyl acetate:hexane (60:40, v: v)
出典と根拠
- ORDレコード
- ord-90c8813362684c10959d03daaddb5777
- 出典データセット
- uspto-grants-2006_09
- 特許番号
- US07102008B2
反応ノート
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