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

HRID 967821

반응식

HRID 967821 반응식
[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]

참가 물질

8

반응물 4

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

생성물 1

HCID 222913982-[4-(2-ethyl-5-methyl-4-phenyl-1H-imidazol-1-yl)phenyl]ethanol수율 23.2%

시약·촉매·용매 3

HCID 887Methanol용매HCID 6344Dichloromethane용매HCID 14798Sodium Hydroxide용매

반응 조건

온도
100 °C

실험 절차

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).

후처리

  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)

출처 및 근거

ORD 기록
ord-9392528715a34da0ad15379c42c8a60e
출처 데이터셋
uspto-grants-2005_10
특허 번호
US06956050B2

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