1-(2-chloro-4-(1-pentyloxy)benzyl)-4-ethenyl-2-methyl-1H-imidazole-5-carbaldehyde → 1-(2-chloro-4-(1-pentyloxy)benzyl)-4-ethyl-2-methyl-1H-imidazole-5-carbaldehyde

HRID 1828819노트

반응식

HRID 1828819 반응식
[Cl:1][C:2]1[CH:18]=[C:17]([O:19][CH2:20][CH2:21][CH2:22][CH2:23][CH3:24])[CH:16]=[CH:15][C:3]=1[CH2:4][N:5]1[C:9]([CH:10]=[O:11])=[C:8]([CH:12]=[CH2:13])[N:7]=[C:6]1[CH3:14]>O1CCOCC1.[C].[Pd]>[Cl:1][C:2]1[CH:18]=[C:17]([O:19][CH2:20][CH2:21][CH2:22][CH2:23][CH3:24])[CH:16]=[CH:15][C:3]=1[CH2:4][N:5]1[C:9]([CH:10]=[O:11])=[C:8]([CH2:12][CH3:13])[N:7]=[C:6]1[CH3:14]

참가 물질

4

실험 절차

1-(2-Chloro-4-(1-pentyloxy)benzyl)-4-ethenyl-2-methyl-1H-imidazole-5-carbaldehyde (575 mg) was dissolved in 1,4-dioxane (6 ml) and palladium carbon (50 mg) was added. The mixture was stirred under a hydrogen atmosphere for 1.5 hr. The reaction mixture was filtered through celite. Water was added to the filtrate and extracted with ethyl acetate. The organic layer was washed with brine, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was applied to silica gel column chromatography and eluted with chloroform/ethyl acetate=2/1. The objective fraction was concentrated under reduced pressure to give 1-(2-chloro-4-(1-pentyloxy)benzyl)-4-ethyl-2-methyl-1H-imidazole-5-carbaldehyde (283 mg) as a black brown oil.

후처리

  1. filtrationThe reaction mixture was filtered through celite
  2. additionWater was added to the filtrate
  3. extractionextracted with ethyl acetate
  4. washThe organic layer was washed with brine
  5. dry with materialdried over anhydrous magnesium sulfate
  6. concentrationconcentrated under reduced pressure
  7. washeluted with chloroform/ethyl acetate=2/1
  8. concentrationThe objective fraction was concentrated under reduced pressure

출처 및 근거

ORD 기록
ord-780b3400cac64ca7bf9d1775b0856bda
출처 데이터셋
uspto-grants-2006_06
특허 번호
US07060721B1

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