Bromine → HCID 21097317, compound

HRID 2109205Notes

Reaction equation

HRID 2109205 reaction equation
[CH3:1][N:2]1[CH:6]=[CH:5][N:4]=[C:3]1[N:7]1[CH2:12][CH2:11][O:10][CH2:9][CH2:8]1.[Br:13]Br>O1CCOCC1.N#N.ClC(Cl)C>[Br:13][C:6]1[N:2]([CH3:1])[C:3]([N:7]2[CH2:12][CH2:11][O:10][CH2:9][CH2:8]2)=[N:4][CH:5]=1

Participants

6

Conditions

Temperature
60 °C

Procedure

4-(1-Methyl-1H-imidazol-2-yl)-morpholine (Nagarajan, K. et al. Indian J. Chem. Sect. B, 21, 10, 1982, 949-952) (1.02 g, 6.08 mmol) was dissolved in 35 mL of 1,4-dioxane under and N2 atmosphere. The mixture was heated to 60° C. and a solution of 0.34 mL (6.4 mmol) of Br2 in 10 mL of dichloroethane was added slowly. The mixture was heated for 1 h, then cooled. The mixture was concentrated and the residue was partitioned between 6.5 mL of 1 N NaOH and 25 mL of EtOAc. The NaOH solution was extracted twice more with EtOAc, and the extracts were washed with NaHCO3 and brine, dried with Na2SO4, filtered, concentrated, and chromatographed (0-4% MeOH (0.5% NH4OH) in CH2Cl2) to provide 464 mg of 4-(5-bromo-1-methyl-1H-imidazol-2-yl)-morpholine.

Workup

  1. temperatureThe mixture was heated for 1 h
  2. temperaturecooled
  3. concentrationThe mixture was concentrated
  4. customthe residue was partitioned between 6.5 mL of 1 N NaOH and 25 mL of EtOAc
  5. extractionThe NaOH solution was extracted twice more with EtOAc
  6. washthe extracts were washed with NaHCO3 and brine
  7. dry with materialdried with Na2SO4
  8. filtrationfiltered
  9. concentrationconcentrated
  10. customchromatographed (0-4% MeOH (0.5% NH4OH) in CH2Cl2)

Sources & evidence

ORD record
ord-4f3c0d71185b4464ad2a12c3529f8eb1
Source dataset
uspto-grants-2009_04
Patent number
US07514458B2

Reaction notes

Loading…