Acetonitrile → 5-bromo-3-(1-ethyl-1H-pyrazol-5-yloxy)picolinonitrile

HRID 534042Notes

Reaction equation

HRID 534042 reaction equation
[Br:1][C:2]1[CH:3]=[C:4]([N+]([O-])=O)[C:5]([C:8]#[N:9])=[N:6][CH:7]=1.[CH2:13]([N:15]1[C:19]([OH:20])=[CH:18][CH:17]=[N:16]1)[CH3:14].C(=O)([O-])[O-].[Na+].[Na+].C(#N)C>C(OCC)(=O)C.C(Cl)(Cl)Cl.CCCCCC>[Br:1][C:2]1[CH:3]=[C:4]([O:20][C:19]2[N:15]([CH2:13][CH3:14])[N:16]=[CH:17][CH:18]=2)[C:5]([C:8]#[N:9])=[N:6][CH:7]=1

Participants

6

Reactant 4

HCID 6342AcetonitrileHCID 10340Sodium CarbonateHCID 27696985-Bromo-3-nitropyridine-2-carbonitrileHCID 178418331HCID 178418331, compound

Product 1

HCID 674858325-bromo-3-(1-ethyl-1H-pyrazol-5-yloxy)picolinonitrileYield 53.3%

Reagents, catalysts & solvents 1

HCID 22239056Ethyl acetate chloroform hexaneSolvent

Procedure

5-Bromo-3-nitropicolinonitrile (24.0 g, 105 mmol), 1-ethyl-1H-pyrazol-5-ol (13.0 g, 116 mmol), and sodium carbonate (11.2 g, 105 mmol) were combined witb acetonitrile (400 ml). The mixture was heated to reflux for 20 hours. The mixture was then cooled to ambient temperature, filtered and evaporated. The residue was dissolved in ethyl acetate (800 ml) and washed with water (3×200 ml) and brine, dried (MgSO4), filtered and evaporated. The crude material was purified over silica gel (15:35:50, then 20:30:50 ethyl acetate/chloroform/hexane) to afford 5-bromo-3-(1-ethyl-1H-pyrazol-5-yloxy)picolinonitrile (16.4 g, 53% yield) as a white solid.

Workup

  1. temperatureThe mixture was heated
  2. temperatureto reflux for 20 hours
  3. filtrationfiltered
  4. customevaporated
  5. dissolutionThe residue was dissolved in ethyl acetate (800 ml)
  6. washwashed with water (3×200 ml) and brine
  7. dry with materialdried (MgSO4)
  8. filtrationfiltered
  9. customevaporated
  10. customThe crude material was purified over silica gel (15:35:50

Sources & evidence

ORD record
ord-3c2d33582d8f489ea20f116bbd8c75b8
Source dataset
uspto-grants-2014_10
Patent number
US08853409B2

Reaction notes

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