Diisopropylethylamine → (2R,3S,5R)-2-(2,2-Dimethylpropoxy)-5-formyl-3-methylmorpholine-4-carboxylic acid tert-butyl ester

HRID 20403

反応式

HRID 20403 の反応式
[C:1]([O:5][C:6]([N:8]1[C@@H:13]([CH2:14][OH:15])[CH2:12][O:11][C@@H:10]([O:16][CH2:17][C:18]([CH3:21])([CH3:20])[CH3:19])[C@@H:9]1[CH3:22])=[O:7])([CH3:4])([CH3:3])[CH3:2].C(N(CC)C(C)C)(C)C.S(=O)(=O)=O.N1C=CC=CC=1>ClCCl.CS(C)=O>[C:1]([O:5][C:6]([N:8]1[C@@H:13]([CH:14]=[O:15])[CH2:12][O:11][C@@H:10]([O:16][CH2:17][C:18]([CH3:21])([CH3:20])[CH3:19])[C@@H:9]1[CH3:22])=[O:7])([CH3:4])([CH3:3])[CH3:2]

参加物

6

実験手順

Add pyridine sulfur trioxide complex (0.42 g) to (2R,3S,5S)-2-(2,2-dimethylpropoxy)-5-hydroxymethyl-3-methylmorpholine-4-carboxylic acid tert-butyl ester (0.46 g, 1.45 mmol) and N,N-diisopropylethylamine (0.66 g, 5.07 mmol) in dichloromethane (1 mL) and dimethylsulfoxide (4 mL) at −2° C. and stir 30 minutes. TLC shows some alcohol remaining. Add more pyridine sulfur trioxide (100 mg) and stir 30 minutes. Pour into ice-cold saturated aqueous sodium chloride and extract with ethyl acetate. Wash the ethyl acetate layer with 1 N aqueous citric acid, saturated aqueous sodium chloride), dry (magnesium sulfate), filter and concentrate to give the title compound as an oil (456 mg).

後処理

  1. stirringstir 30 minutes
  2. additionPour into ice-cold saturated aqueous sodium chloride
  3. extractionextract with ethyl acetate
  4. washWash the ethyl acetate layer with 1 N aqueous citric acid, saturated aqueous sodium chloride),
  5. dry with materialdry (magnesium sulfate)
  6. filtrationfilter
  7. concentrationconcentrate

出典と根拠

ORDレコード
ord-3e48c768ad554b59a51e4f94284c503d
出典データセット
uspto-grants-2010_06
特許番号
US07745438B2

関連ノート

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