Hydrogen Bromide → HCID 131731313, compound

HRID 1406034Notes

Reaction equation

HRID 1406034 reaction equation
C[O:2][C:3]1[N:8]=[C:7]([C:9]([O:11]C)=[O:10])[CH:6]=[CH:5][C:4]=1[N:13]1[CH:17]=[C:16]([CH3:18])[N:15]=[CH:14]1.[BrH:19]>C(O)(=O)C>[BrH:19].[CH3:18][C:16]1[N:15]=[CH:14][N:13]([C:4]2[C:3](=[O:2])[NH:8][C:7]([C:9]([OH:11])=[O:10])=[CH:6][CH:5]=2)[CH:17]=1

Participants

4

Reactant 2

HCID 260Hydrogen BromideHCID 67798582Methyl 6-methoxy-5-(4-methyl-1H-imidazol-1-yl)pyridine-2-carboxylate

Product 1

HCID 131731313HCID 131731313, compound

Reagents, catalysts & solvents 1

HCID 176Acetic AcidSolvent

Procedure

A solution of C2 (3.82 g, 15.9 mmol) in acetic acid (30 mL) and aqueous hydrobromic acid (48%, 30 mL) was heated at reflux for 4 hours. The reaction was allowed to cool to room temperature, and then chilled in an ice bath; the resulting precipitate was collected via filtration and washed with ice water (30 mL). Recrystallization from ethanol (20 mL) provided the title compound as a light yellow solid. Yield: 3.79 g, 12.6 mmol, 79%. LCMS m/z 220.1 (M+1). 1H NMR (400 MHz, DMSO-d6) δ 12.6 (ν br s, 1H), 9.58-9.60 (m, 1H), 8.07 (d, J=7.6 Hz, 1H), 7.88-7.91 (m, 1H), 7.09 (d, J=7.4 Hz, 1H), 2.34 (br s, 3H).

Workup

  1. temperatureat reflux for 4 hours
  2. temperaturechilled in an ice bath
  3. filtrationthe resulting precipitate was collected via filtration
  4. washwashed with ice water (30 mL)
  5. customRecrystallization from ethanol (20 mL)

Sources & evidence

ORD record
ord-a3439376b21941aca129d2ec70d3962e
Source dataset
uspto-grants-2014_12
Patent number
US08916564B2

Reaction notes

Loading…