Reaction #487517

ord-af73a0d77efb4ca3aeadec24f017d7c2

Reaction equation

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

Solvents

Conditions

Detailed conditions
See reaction.notes.procedure_details.

Workup

  1. 1
    OtherSolvents were removed under the reduced pressure
  2. 2
    workup.DISSOLUTIONthe resulting residue was dissolved in dichloromethane (50 mL)
  3. 3
    Washwashed with water, saturated ammonia chloride, brine
  4. 4
    Dryingdried over sodium sulfate
  5. 5
    Concentrationconcentrated
  6. 6
    OtherThe residue was purified by silica gel chromatography
  7. 7
    Washeluting with 1:1 hexane-ethyl acetate
  8. 8
    Otherto give V (640 mg, 85%) as a white foam

Procedure

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.

Source

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08741567B2uspto-grants-2014_06