Ammonium Acetate → 7-[5-(2-methoxyphenyl)-1H-imidazol-2-yl]heptanoic acid methyl ester

HRID 1616549Notes

Reaction equation

HRID 1616549 reaction equation
C([O-])(=O)C.[NH4+:5].[CH3:6][O:7][C:8](=[O:29])[CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][C:15](=O)[NH:16][CH2:17][C:18]([C:20]1[CH:25]=[CH:24][CH:23]=[CH:22][C:21]=1[O:26][CH3:27])=O>C(O)(=O)C>[CH3:6][O:7][C:8](=[O:29])[CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][C:15]1[NH:5][C:18]([C:20]2[CH:25]=[CH:24][CH:23]=[CH:22][C:21]=2[O:26][CH3:27])=[CH:17][N:16]=1

Participants

4

Procedure

Heat a mixture of ammonium acetate (16.5 g, 214 mmol) and 7-[2-(2-methoxyphenyl)-2-oxoethylcarbamoyl]heptanoic acid methyl ester (14.2 g, 42.3 mmol) in acetic acid (300 mL) at reflux under nitrogen for 15 hours. Remove the solvent under reduced pressure. Dilute the residue in ethyl acetate (500 mL) and adjust to pH 8 with saturated aqueous sodium bicarbonate solution. Extract the aqueous layer with additional ethyl acetate (200 mL) and dry the combined organic extracts over sodium sulfate and remove the solvent under reduced pressure. Purify the residue by flash column chromatography on silica gel, eluting with ethyl acetate, to afford 7-[5-(2-methoxyphenyl)-1H-imidazol-2-yl]heptanoic acid methyl ester (5.86 g, 44%): APCI mass spectrum m/z 317 [C18H24N2O3+H]+.

Workup

  1. temperatureHeat
  2. temperatureat reflux under nitrogen for 15 hours
  3. customRemove the solvent under reduced pressure
  4. additionDilute the residue in ethyl acetate (500 mL)
  5. extractionExtract the aqueous layer with additional ethyl acetate (200 mL)
  6. dry with materialdry the combined organic extracts over sodium sulfate
  7. customremove the solvent under reduced pressure
  8. customPurify the residue by flash column chromatography on silica gel
  9. washeluting with ethyl acetate

Sources & evidence

ORD record
ord-f5c51872cb424c24b380acc96e1ad7e9
Source dataset
uspto-grants-2014_07
Patent number
US08765796B2

Reaction notes

Loading…