Ammonium Acetate → 7-[5-(2-methoxyphenyl)-1H-imidazol-2-yl]heptanoic acid methyl ester
반응식
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]=1참가 물질
실험 절차
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]+.
후처리
- temperatureHeat
- temperatureat reflux under nitrogen for 15 hours
- customRemove the solvent under reduced pressure
- additionDilute the residue in ethyl acetate (500 mL)
- extractionExtract the aqueous layer with additional ethyl acetate (200 mL)
- dry with materialdry the combined organic extracts over sodium sulfate
- customremove the solvent under reduced pressure
- customPurify the residue by flash column chromatography on silica gel
- washeluting with ethyl acetate
출처 및 근거
- ORD 기록
- ord-0a58340062ce42dea444b2771bc9ba7e
- 출처 데이터셋
- uspto-grants-2013_10
- 특허 번호
- US08552039B2
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