Sodium Bicarbonate → ethyl 2-(2,4-dichlorophenyl)-5-methyl-1-(4-(trifluoromethyl)phenyl)-1H-imidazole-4-carboxylate

HRID 2215059Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 2215059
[Cl:1][C:2]1[CH:7]=[C:6]([Cl:8])[CH:5]=[CH:4][C:3]=1[C:9]([NH:11][C:12]1[CH:17]=[CH:16][C:15]([C:18]([F:21])([F:20])[F:19])=[CH:14][CH:13]=1)=[NH:10].Br[CH:23]([CH3:31])[C:24](=O)[C:25]([O:27][CH2:28][CH3:29])=[O:26].C([O-])(O)=O.[Na+]>CC(O)C>[Cl:1][C:2]1[CH:7]=[C:6]([Cl:8])[CH:5]=[CH:4][C:3]=1[C:9]1[N:11]([C:12]2[CH:13]=[CH:14][C:15]([C:18]([F:21])([F:19])[F:20])=[CH:16][CH:17]=2)[C:23]([CH3:31])=[C:24]([C:25]([O:27][CH2:28][CH3:29])=[O:26])[N:10]=1

Komponenten

5

Versuchsvorschrift

Part C: 2,4-Dichloro-N-(4-(trifluoromethyl)phenyl)benzenecarboxamidine (15.0 g, 0.0450 mol) is dissolved in 2-propanol and ethyl 3-bromo-2-oxobutanoate (20.8 g, 2 molar equivalent) and NaHCO3 are successively added. The resulting mixture is heated at reflux temperature for 40 hours and allowed to attain room temperature. The 2-propanol is removed in vacuo, ethyl acetate is added to the residue and the resulting organic layer is washed with NaHCO3 (5% aqueous solution). The ethylacetate layer is collected, dried over Na2SO4, filtered and concentrated in vacuo. The resulting oil is purified by column chromatography (diethyl ether/petroleum ether=1/3 (v/v), silicagel) and further purified by crystallisation from cyclohexane to give ethyl 2-(2,4-dichlorophenyl)-5-methyl-1-(4-(trifluoromethyl)phenyl)-1H-imidazole-4-carboxylate (10.45 g, 52% yield) as a yellow solid. Melting point: 160–162° C.

Aufarbeitung

  1. temperatureThe resulting mixture is heated
  2. temperatureat reflux temperature for 40 hours
  3. customto attain room temperature
  4. customThe 2-propanol is removed in vacuo, ethyl acetate
  5. additionis added to the residue
  6. washthe resulting organic layer is washed with NaHCO3 (5% aqueous solution)
  7. customThe ethylacetate layer is collected
  8. dry with materialdried over Na2SO4
  9. filtrationfiltered
  10. concentrationconcentrated in vacuo
  11. customThe resulting oil is purified by column chromatography (diethyl ether/petroleum ether=1/3 (v/v), silicagel)
  12. customfurther purified by crystallisation from cyclohexane

Quellen und Nachweise

ORD-Eintrag
ord-58c26c34d65c4df3bd3b9c7b2ac97887
Quelldatensatz
uspto-grants-2006_09
Patentnummer
US07109216B2

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