Acetic Acid → 2-[4-(2-ethyl-5-methyl-4-phenyl-1H-imidazol-1-yl)phenyl]ethanol

HRID 967821

Reaktionsgleichung

Reaktionsgleichung von HRID 967821
[OH:1][CH2:2][CH2:3][C:4]1[CH:9]=[CH:8][C:7]([NH:10][CH:11]([CH3:20])[C:12]([C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=2)=O)=[CH:6][CH:5]=1.[C:21](Cl)(=O)[CH2:22][CH3:23].C([O-])(=O)C.[NH4+:30].CC(O)=O>ClCCl.CO.[OH-].[Na+]>[CH2:22]([C:21]1[N:10]([C:7]2[CH:8]=[CH:9][C:4]([CH2:3][CH2:2][OH:1])=[CH:5][CH:6]=2)[C:11]([CH3:20])=[C:12]([C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=2)[N:30]=1)[CH3:23]

Komponenten

8

Edukt 4

HCID 176Acetic AcidHCID 62324Propionyl chlorideHCID 517165Ammonium AcetateHCID 222913492-{[4-(2-Hydroxyethyl)phenyl]amino}-1-phenyl-1-propanone

Produkt 1

HCID 222913982-[4-(2-ethyl-5-methyl-4-phenyl-1H-imidazol-1-yl)phenyl]ethanolAusbeute 23,2 %

Reagenzien, Katalysatoren, Lösungsmittel 3

HCID 887MethanolLösungsmittelHCID 6344DichloromethaneLösungsmittelHCID 14798Sodium HydroxideLösungsmittel

Reaktionsbedingungen

Temperatur
100 °C

Versuchsvorschrift

To a stirred solution of 2-{[4-(2-hydroxyethyl)phenyl]amino}-1-phenyl-1-propanone (step 1 in EXAMPLE 3, 1.2 g, 4.5 mmol) in dichloromethane (10 mL) was added propionyl chloride (1.0 mL, 11.1 mmol) at ambient temperature. After 1 h, the reaction mixture was partitioned between ethyl acetate (30 mL) and water (10 mL). The aqueous phase was extracted with ethyl acetate (3×30 mL) and the combined organic phase was dried (MgSO4) and concentrated under reduced pressure. To the residue was added ammonium acetate (7.7 g, 100 mmol) and AcOH (15 mL) and the mixture was heated at 100° C. for 10 h. After cooling, the mixture was diluted with MeOH and basified with 4N NaOH aq. at 0° C. After 30 min, volatile components were removed under reduced pressure. The aqueous phase was extracted with dichloromethane (4×20 mL) and the combined organic phase was dried (MgSO4) and concentrated under reduced pressure. Purification by flash column chromatography on silica gel eluting with hexane/ethyl acetate (gradient elution from 1:1 to 1:2) to afford 0.32 g (23%) of the title compound as brown amorphous: 1H-NMR (CDCl3)δ1.19 (3H, t, J=7.5 Hz), 2.16 (3H, s), 2.57 (3H, q, J=7.5 Hz), 2.97 (2H, t, J=6.4 Hz), 3.96 (2H, t, J=6.4 Hz), 7.19-7.26 (3H, m), 7.38-7.43 (4H, m), 7.79 (2H, dd, J=7.1, 1.4 Hz).

Aufarbeitung

  1. customthe reaction mixture was partitioned between ethyl acetate (30 mL) and water (10 mL)
  2. extractionThe aqueous phase was extracted with ethyl acetate (3×30 mL)
  3. dry with materialthe combined organic phase was dried (MgSO4)
  4. concentrationconcentrated under reduced pressure
  5. temperatureAfter cooling
  6. waitAfter 30 min
  7. customvolatile components were removed under reduced pressure
  8. extractionThe aqueous phase was extracted with dichloromethane (4×20 mL)
  9. dry with materialthe combined organic phase was dried (MgSO4)
  10. concentrationconcentrated under reduced pressure
  11. customPurification by flash column chromatography on silica gel eluting with hexane/ethyl acetate (gradient elution from 1:1 to 1:2)

Quellen und Nachweise

ORD-Eintrag
ord-9392528715a34da0ad15379c42c8a60e
Quelldatensatz
uspto-grants-2005_10
Patentnummer
US06956050B2

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