Imidazole → HCID 67442185, compound

HRID 1667320Notes

Reaction equation

HRID 1667320 reaction equation
[NH:1]1[CH:5]=[CH:4][N:3]=[CH:2]1.C(=O)([O-])[O-].[K+].[K+].Cl[CH2:13][C:14]([N:16]1[CH2:21][CH2:20][CH:19](/[CH:22]=[CH:23]/[C:24]2[C:29]([CH3:30])=[CH:28][CH:27]=[CH:26][C:25]=2[CH3:31])[CH2:18][CH2:17]1)=[O:15].C(=O)([O-])O.[Na+]>C(#N)C>[CH3:31][C:25]1[CH:26]=[CH:27][CH:28]=[C:29]([CH3:30])[C:24]=1/[CH:23]=[CH:22]/[CH:19]1[CH2:20][CH2:21][N:16]([C:14](=[O:15])[CH2:13][N:1]2[CH:5]=[CH:4][N:3]=[CH:2]2)[CH2:17][CH2:18]1

Participants

6

Reactant 4

HCID 795ImidazoleHCID 11430Potassium CarbonateHCID 516892Sodium BicarbonateHCID 10402058HCID 10402058, compound

Product 1

HCID 67442185HCID 67442185, compoundYield 94.4%

Reagents, catalysts & solvents 1

HCID 6342AcetonitrileSolvent

Procedure

84 mg of 1H-imidazole and 142 mg of potassium carbonate were added to a solution of 300 mg of 1-(chloroacetyl)-4-[(E)-2-(2,6-dimethylphenyl)vinyl]piperidine in 5 ml of acetonitrile, followed by heating under reflux for 3 hours. After cooling, saturated aqueous sodium hydrogencarbonate solution was added to the reaction mixture, followed by extraction with chloroform. The organic layer was concentrated under reduced pressure and the residue was purified by silica gel column chromatography (chloroform-methanol-ammonia water) to give 314 mg of 4-[(E)-2-(2,6-dimethylphenyl)vinyl]-1-(1H-imidazol-1-ylacetyl)piperidine as yellow crystals. A portion of 288 mg from the crystals was dissolved in 2 ml of ethanol and 334 μl of 4N hydrochloric acid-ethyl acetate was added to the solution, followed by concentrating under reduced pressure. The residue was crystallized from ethanol-diethyl ether and the crystals were collected by filtration. The crystals were then washed with diethyl ether. The crystals were recrystallized from ethanol-diethyl ether to give 188 mg of 4-[(E)-2-(2,6-dimethylphenyl)vinyl]-1-(1H-imidazol-1-ylacetyl)piperidine monohydrochloride.

Workup

  1. temperatureby heating
  2. temperatureunder reflux for 3 hours
  3. temperatureAfter cooling
  4. extractionfollowed by extraction with chloroform
  5. concentrationThe organic layer was concentrated under reduced pressure
  6. customthe residue was purified by silica gel column chromatography (chloroform-methanol-ammonia water)

Sources & evidence

ORD record
ord-40c89a0b8c6e4cbfbf4a9b2cc1af630f
Source dataset
uspto-grants-2011_10
Patent number
US08044206B2

Reaction notes

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