Sodium Azide → HCID 22710915, compound

HRID 352811Notes

Reaction equation

HRID 352811 reaction equation
[Si:1]([O:8][C:9]1[C:10](=[O:17])[CH:11]=[C:12]([CH2:15]Cl)[O:13][CH:14]=1)([C:4]([CH3:7])([CH3:6])[CH3:5])([CH3:3])[CH3:2].[N-:18]=[N+]=[N-].[Na+]>CN(C)C=O>[Si:1]([O:8][C:9]1[C:10](=[O:17])[CH:11]=[C:12]([CH2:15][NH2:18])[O:13][CH:14]=1)([C:4]([CH3:7])([CH3:6])[CH3:5])([CH3:3])[CH3:2]

Participants

4

Procedure

In N,N-dimethylformamide (20 ml) was dissolved (5-tert-butyldimethylsilyloxy-4-oxo-4H-pyran-2-yl)methyl chloride (2.00 g). Sodium azide (1.00 g) was added to the resulting solution and the resulting mixture was stirred overnight at room temperature. The reaction mixture was concentrated under reduced pressure. Ethyl acetate was added to the residue, followed by washing once with water and then once with saturated aqueous NaCl solution. The organic layer thus extracted was dried over anhydrous sodium sulfate and distilled under reduced pressure to remove the solvent. The resulting residue was dissolved in methanol (100 ml), followed by the addition of 10% palladium-carbon (50% wet w/w, 800 mg). The resulting mixture was stirred overnight under a hydrogen gas stream of normal pressure. The reaction mixture was subjected to Celite filtration, the filtrate was concentrated under reduced pressure and the residue was purified by chromatography on a silica gel column (methylene chloride methanol=100:3), whereby the title compound (290 mg) was obtained as a colorless oil.

Workup

  1. concentrationThe reaction mixture was concentrated under reduced pressure
  2. additionEthyl acetate was added to the residue
  3. washby washing once with water
  4. extractionThe organic layer thus extracted
  5. dry with materialwas dried over anhydrous sodium sulfate
  6. distillationdistilled under reduced pressure
  7. customto remove the solvent
  8. dissolutionThe resulting residue was dissolved in methanol (100 ml)
  9. additionfollowed by the addition of 10% palladium-carbon (50% wet w/w, 800 mg)
  10. stirringThe resulting mixture was stirred overnight under a hydrogen gas stream of normal pressure
  11. filtrationThe reaction mixture was subjected to Celite filtration
  12. concentrationthe filtrate was concentrated under reduced pressure
  13. customthe residue was purified by chromatography on a silica gel column (methylene chloride methanol=100:3), whereby the title compound (290 mg)
  14. customwas obtained as a colorless oil

Sources & evidence

ORD record
ord-c9645acd674e4a91b87a153cfc78282c
Source dataset
uspto-grants-2004_06
Patent number
US06747023B1

Reaction notes

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