反応 #487517

ord-af73a0d77efb4ca3aeadec24f017d7c2

反応方程式

CC(=O)O[C@H]1O[C@H](CN=[N+]=[N-])[C@@H](OC(C)=O)[C@H](OC(C)=O)[C@H]1OC(C)=O
1,2,3,4-tetra-O-acetyl-6-azido-6-deoxy-α-D-glucopyranose
NCc1ccccc1
benzylamine
CC(=O)O[C@@H]1[C@@H](OC(C)=O)[C@@H](O)O[C@H](CN=[N+]=[N-])[C@H]1OC(C)=O
2,3,4-tri-O-acetyl-6-azido-6-deoxy-α-D-glucopyranose

溶媒

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    その他Solvents were removed under the reduced pressure
  2. 2
    workup.DISSOLUTIONthe resulting residue was dissolved in dichloromethane (50 mL)
  3. 3
    洗浄washed with water, saturated ammonia chloride, brine
  4. 4
    乾燥dried over sodium sulfate
  5. 5
    濃縮concentrated
  6. 6
    その他The residue was purified by silica gel chromatography
  7. 7
    洗浄eluting with 1:1 hexane-ethyl acetate
  8. 8
    その他to give V (640 mg, 85%) as a white foam

実験手順

To a solution of 1,2,3,4-tetra-O-acetyl-6-azido-6-deoxy-α-D-glucopyranose (IV, 850 mg, 2.78 mmol) in THF (12 mL) was added benzylamine (0.23 mL) and the mixture was stirred at rt overnight. Solvents were removed under the reduced pressure and the resulting residue was dissolved in dichloromethane (50 mL) and washed with water, saturated ammonia chloride, brine, dried over sodium sulfate and concentrated. The residue was purified by silica gel chromatography, eluting with 1:1 hexane-ethyl acetate, to give V (640 mg, 85%) as a white foam. 1H NMR (500.1 MHz) (CD3Cl) δ: 5.50 (m, 2H), 5.03 (t, J=10.5 Hz, 1H), 4.90 (m, 1H), 4.24 (m, 1H), 3.35 (m, 2H), 2.12 (s, 3H), 2.05 (s, 3H), 2.02 (s, 3H). 13C NMR (125.8 MHz) (CDCl3) δ: 170.26, 170.23, 169.78, 89.98, 71.09, 69.71, 68.34, 51.05, 20.68, 20.62, 20.58.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US08741567B2uspto-grants-2014_06