Sodium Azide → HCID 85939649, compound

HRID 749249Notes

Reaction equation

HRID 749249 reaction equation
Br[CH2:2][C:3]([C:5]1[CH:10]=[CH:9][C:8]([O:11][CH2:12][C:13]2[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=2)=[C:7]([F:19])[CH:6]=1)=[O:4].[N-:20]=[N+:21]=[N-:22].[Na+]>CN(C=O)C>[N:20]([CH2:2][C:3]([C:5]1[CH:10]=[CH:9][C:8]([O:11][CH2:12][C:13]2[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=2)=[C:7]([F:19])[CH:6]=1)=[O:4])=[N+:21]=[N-:22]

Participants

4

Procedure

A solution of 2-bromo-1-[4-(benzyloxy)-3-fluorophenyl]ethanone (J. Med. Chem. 1980, 23, 738-744) (1 g) in dry DMF (2.5 mL) was cooled to 15° C. and treated portionwise with sodium azide (220 mg). After complete addition the reaction mixture was stirred for a further 1 h. The reaction mixture was partitioned between EtOAc and water. The organic phase was washed with water and the combined aqueous phase back extracted with EtOAc. The combined organic phase was washed with sat. NaHCO3(aq) three times and the combined washes back extracted with EtOAc. The combined organic phase was washed with brine, dried and concentrated in vacuo. The residue was purified by column chromatography on silica, eluting with hexane-EtOAc (4:1 and 2:1) to give the title compound (810 mg). LCMS RT=3.61 min.

Workup

  1. additionAfter complete addition the reaction mixture
  2. customThe reaction mixture was partitioned between EtOAc and water
  3. washThe organic phase was washed with water
  4. extractionthe combined aqueous phase back extracted with EtOAc
  5. washThe combined organic phase was washed with sat. NaHCO3(aq) three times
  6. extractionthe combined washes back extracted with EtOAc
  7. washThe combined organic phase was washed with brine
  8. customdried
  9. concentrationconcentrated in vacuo
  10. customThe residue was purified by column chromatography on silica
  11. washeluting with hexane-EtOAc (4:1 and 2:1)

Sources & evidence

ORD record
ord-1cbb6495096f46c7b6742f83e0d43636
Source dataset
uspto-grants-2008_07
Patent number
US07402598B2

Reaction notes

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