Cesium carbonate → 3-chloro-2-[(1R)-2,2,2-trifluoro-1-methylethoxy]pyridine

HRID 2048100ノート

反応式

HRID 2048100 の反応式
[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

5

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

  1. stirringthe mixture stirred at the same temperature for another 2.5 hours
  2. temperatureThe reaction mixture was cooled to room temperature
  3. custompartitioned between water and EtOAc
  4. customThe organic phase was separated
  5. washwashed with brine (2×30 mL)
  6. dry with materialdried over Na2SO4
  7. filtrationfiltered
  8. concentrationconcentrated in vacuo
  9. customto give a crude product as colourless oil
  10. customThe crude product was purified by silica gel column chromatography
  11. 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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