Calcium Chloride → 6-Amino-1-methyl-2-(((1-propylimidazol-5-yl)methyl)sulfanyl)benzimidazole

HRID 856798노트

반응식

HRID 856798 반응식
[CH3:1][N:2]1[C:6]2[CH:7]=[C:8]([N+:11]([O-])=O)[CH:9]=[CH:10][C:5]=2[N:4]=[C:3]1[S:14][CH2:15][C:16]1[N:20]([CH2:21][CH2:22][CH3:23])[CH:19]=[N:18][CH:17]=1.[Cl-].[Ca+2].[Cl-]>C(O)C>[NH2:11][C:8]1[CH:9]=[CH:10][C:5]2[N:4]=[C:3]([S:14][CH2:15][C:16]3[N:20]([CH2:21][CH2:22][CH3:23])[CH:19]=[N:18][CH:17]=3)[N:2]([CH3:1])[C:6]=2[CH:7]=1

참가 물질

4

실험 절차

An aqueous solution of 1-methyl-6-nitro-2-(((1-propylimidazol-5-yl)methyl)sulfanyl)benzimidazole (230 mg), reduced iron (194 mg) and anhydrous calcium chloride (38.5 mg) in 85% ethanol (10 ml) was stirred for 1 day under nitrogen atmosphere at 105° C. The mixture was allowed to be at room temperature, the insolubles were filtered off, water was added to the mixture, and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine and dried over magnesium sulfate, and the solvent was distilled off under reduced pressure. The obtained residue was purified by basic silica gel column chromatography (ethyl acetate) to give 6-amino-1-methyl-2-(((1-propylimidazol-5-yl)methyl)sulfanyl)benzimidazole (170 mg) as colorless oil.

후처리

  1. customto be at room temperature
  2. filtrationthe insolubles were filtered off
  3. additionwater was added to the mixture
  4. extractionthe mixture was extracted with ethyl acetate
  5. washThe organic layer was washed with saturated brine
  6. dry with materialdried over magnesium sulfate
  7. distillationthe solvent was distilled off under reduced pressure
  8. customThe obtained residue was purified by basic silica gel column chromatography (ethyl acetate)

출처 및 근거

ORD 기록
ord-b871b540f86049308b0d46d06656393e
출처 데이터셋
uspto-grants-2007_08
특허 번호
US07262185B2

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