Hydrochloric Acid → 4-chloro-1-(4-methoxybutyl)-2-phenyl-1H-imidazole-5-carboxylic acid

HRID 1184213노트

반응식

HRID 1184213 반응식
[Cl:1][C:2]1[N:3]=[C:4]([C:15]2[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=2)[N:5]([CH2:9][CH2:10][CH2:11][CH2:12][O:13][CH3:14])[C:6]=1[CH:7]=[O:8].Cl([O-])=[O:22].[Na+].P([O-])(O)(O)=O.[Na+].Cl>C(O)(C)(C)C.CC(=CC)C>[Cl:1][C:2]1[N:3]=[C:4]([C:15]2[CH:16]=[CH:17][CH:18]=[CH:19][CH:20]=2)[N:5]([CH2:9][CH2:10][CH2:11][CH2:12][O:13][CH3:14])[C:6]=1[C:7]([OH:22])=[O:8]

참가 물질

7

실험 절차

To a solution of 4-chloro-1-(4-methoxybutyl)-2-phenyl-1H-imidazole-5-carbaldehyde (790 mg) in tert-butanol (15 ml) and 2-methyl-2-butene (1.5 ml) was added aqueous solution (4 ml) of sodium chlorite (300 mg) and sodium dihydrogen phosphate (400 mg), and the mixture was stirred at room temperature for 12 hr. 1M Hydrochloric acid was added, and the mixture was adjusted to pH 3, and extracted with ethyl acetate. The extract was washed with saturated brine, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure to give the object product (730 mg).

후처리

  1. extractionextracted with ethyl acetate
  2. washThe extract was washed with saturated brine
  3. dry with materialdried over anhydrous magnesium sulfate
  4. customThe solvent was evaporated under reduced pressure

출처 및 근거

ORD 기록
ord-9586d79f214041f29ca991880f68e9b6
출처 데이터셋
uspto-grants-2014_03
특허 번호
US08664380B2

반응 노트

불러오는 중…