Methanesulfonyl chloride → (S)-[[(Methylsulfonyl)oxy]methyl]piperidine-1-carboxylic Acid tert-Butyl Ester

HRID 272095ノート

反応式

HRID 272095 の反応式
[C:1]([O:5][C:6]([N:8]1[CH2:13][CH2:12][CH2:11][C@H:10]([CH2:14][OH:15])[CH2:9]1)=[O:7])([CH3:4])([CH3:3])[CH3:2].[CH3:16][S:17](Cl)(=[O:19])=[O:18]>C(Cl)(Cl)Cl.C(N(CC)CC)C>[CH3:16][S:17]([O:15][CH2:14][C@H:10]1[CH2:11][CH2:12][CH2:13][N:8]([C:6]([O:5][C:1]([CH3:4])([CH3:3])[CH3:2])=[O:7])[CH2:9]1)(=[O:19])=[O:18]

参加物

5

実験手順

To a solution of 7.96 g of {(3S)-1-(tert-butoxycarbonyl)-3-piperidyl}methanol in 150 ml of chloroform, 3.4 ml of methanesulfonyl chloride and 6.7 ml of triethylamine were added under cooling with ice, followed by an hour's stirring at room temperature. The reaction liquid was distilled off under reduced pressure, diluted with ethyl acetate and saturated aqueous sodium bicarbonate solution was added, followed by 1.5 hours' stirring. Thereafter the reaction liquid was successively washed with water and saturated brine and dried over anhydrous magnesium sulfate. Distilling the solvent off, 10.50 g of the title compound was obtained.

後処理

  1. temperatureunder cooling with ice
  2. waitfollowed by an hour
  3. customThe reaction liquid
  4. distillationwas distilled off under reduced pressure
  5. additiondiluted with ethyl acetate and saturated aqueous sodium bicarbonate solution
  6. additionwas added
  7. stirring' stirring
  8. customThereafter the reaction liquid
  9. washwas successively washed with water and saturated brine
  10. dry with materialdried over anhydrous magnesium sulfate
  11. distillationDistilling the solvent off, 10.50 g of the title compound
  12. customwas obtained

出典と根拠

ORDレコード
ord-ca7c0447b0a8472bad456b9a69a843df
出典データセット
uspto-grants-2008_11
特許番号
US07452908B2

反応ノート

読み込み中…