Cesium carbonate → 3-chloro-2-[(1R)-2,2,2-trifluoro-1-methylethoxy]pyridine
反応式
[Cl:1][C:2]1[C:3](F)=[N:4][CH:5]=[CH:6][CH:7]=1.[F:9][C:10]([F:15])([F:14])[C@H:11]([OH:13])[CH3:12].C([O-])([O-])=O.[Cs+].[Cs+]>CS(C)=O>[Cl:1][C:2]1[C:3]([O:13][C@H:11]([CH3:12])[C:10]([F:15])([F:14])[F:9])=[N:4][CH:5]=[CH:6][CH:7]=1参加物
反応条件
- 温度
- 80 °C
実験手順
To a solution of 3-chloro-2-fluoropyridine (500 mg, 3.8 mmol) and (2R)-1,1,1-trifluoropropan-2-ol (75 wt % solution in TBME, 752 mg, 4.9 mmol) in DMSO (7 mL) was added Cs2CO3 (1.6 g, 4.9 mmol) at room temperature under N2. The resulting mixture was stirred at 80° C. for 2 hours. To the reaction mixture was added another 500 mg of (2R)-1,1,1-trifluoropropan-2-ol and the mixture stirred at the same temperature for another 2.5 hours. The reaction mixture was cooled to room temperature, and partitioned between water and EtOAc. The organic phase was separated, washed with brine (2×30 mL), dried over Na2SO4, filtered, and concentrated in vacuo to give a crude product as colourless oil. The crude product was purified by silica gel column chromatography eluting with 0-30% EtOAc in heptane to give the title compound (365 mg, 43%) as colourless oil.
後処理
- stirringthe mixture stirred at the same temperature for another 2.5 hours
- temperatureThe reaction mixture was cooled to room temperature
- custompartitioned between water and EtOAc
- customThe organic phase was separated
- washwashed with brine (2×30 mL)
- dry with materialdried over Na2SO4
- filtrationfiltered
- concentrationconcentrated in vacuo
- customto give a crude product as colourless oil
- customThe crude product was purified by silica gel column chromatography
- washeluting with 0-30% EtOAc in heptane
出典と根拠
- ORDレコード
- ord-d9f9c76a300740808397182f3b6ed882
- 出典データセット
- uspto-grants-2013_11
- 特許番号
- US08592629B2
反応ノート
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