O-Phenylenediamine → 2-(6-hydroxyheptyl)-1H-benzimidazole

HRID 2414788노트

반응식

HRID 2414788 반응식
O[CH:2]([CH3:11])[CH2:3][CH2:4][CH2:5][CH2:6][C:7]([O:9]C)=O.[C:12]1([NH2:19])[CH:17]=[CH:16][CH:15]=[CH:14][C:13]=1[NH2:18].[OH-].[Na+].[C:22](=O)([O-])O.[Na+]>Cl.O>[OH:9][CH:7]([CH3:22])[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2][C:11]1[NH:19][C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][C:13]=2[N:18]=1

참가 물질

7

실험 절차

3.28 g of methyl 6-hydroxyheptanoate and 2.16 g of phenylenediamine were dissolved in a mixed solvent of 10 ml of concentrated hydrochloric acid and 20 ml of water, and the mixture was refluxed with stirring under heating for 24 hours. After cooling to room temperature, the reaction mixture was adjusted to pH 8 with about 100 ml of 1 N sodium hydroxide solution and saturated aqueous sodium hydrogencarbonate. The reaction mixture was extracted three times with 150 ml of ethyl acetate, and the organic layer was washed with saturated brine and dried over sodium sulfate. After the solvent was evaporated under reduced pressure, the residue was purified by silica gel column chromatography (ethyl acetate—ethyl acetate:methanol=95:5) to obtain 3.03 g of the title compound as pale brown solid (yield: 70%).

후처리

  1. temperaturethe mixture was refluxed
  2. temperatureunder heating for 24 hours
  3. extractionThe reaction mixture was extracted three times with 150 ml of ethyl acetate
  4. washthe organic layer was washed with saturated brine
  5. dry with materialdried over sodium sulfate
  6. customAfter the solvent was evaporated under reduced pressure
  7. customthe residue was purified by silica gel column chromatography (ethyl acetate—ethyl acetate:methanol=95:5)

출처 및 근거

ORD 기록
ord-ee688e649acc4f45a02be7b9f5f62125
출처 데이터셋
uspto-grants-2004_11
특허 번호
US06815455B1

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