Dimethylamine → (S)-2-tert-Butoxycarbonylamino-4-dimethylaminobutyric acid methyl ester

HRID 2112188ノート

反応式

HRID 2112188 の反応式
[CH3:1][O:2][C:3](=[O:16])[C@@H:4]([NH:8][C:9]([O:11][C:12]([CH3:15])([CH3:14])[CH3:13])=[O:10])[CH2:5][CH2:6]Br.[CH2:17]([N:19](CC)[CH2:20]C)C.CNC>C1COCC1>[CH3:1][O:2][C:3](=[O:16])[C@@H:4]([NH:8][C:9]([O:11][C:12]([CH3:15])([CH3:14])[CH3:13])=[O:10])[CH2:5][CH2:6][N:19]([CH3:20])[CH3:17]

参加物

5

反応条件

温度
60 °C

実験手順

To a solution of (S)-4-bromo-2-tert-butoxycarbonylaminobutyric acid methyl ester (27.5 g, 93 mmol) in THF (100 mL) in a pressure reaction vessel was added triethylamine (26 mL) and dimethylamine (93 mL of 2.0 M in THF). The reaction vessel was sealed and heated to 60° C. for 16 hours and then cooled to room temperature. The reaction mixture was concentrated under reduced pressure and then dissolved in dichloromethane (500 mL). The solution was washed with water (3×200 mL) and brine (200 mL), dried over MgSO4, filtered through Celite and concentrated under reduced pressure. The residue was dried under high vacuum to afford 23.4 g of yellow oil (97% yield).

後処理

  1. customThe reaction vessel was sealed
  2. temperaturecooled to room temperature
  3. concentrationThe reaction mixture was concentrated under reduced pressure
  4. dissolutiondissolved in dichloromethane (500 mL)
  5. washThe solution was washed with water (3×200 mL) and brine (200 mL)
  6. dry with materialdried over MgSO4
  7. filtrationfiltered through Celite
  8. concentrationconcentrated under reduced pressure
  9. customThe residue was dried under high vacuum

出典と根拠

ORDレコード
ord-b88e26d83f9a47d3aa4d838f67e98361
出典データセット
uspto-grants-2009_04
特許番号
US07521447B2

反応ノート

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