Acetic Acid → N-{[2-(2,4-Dichloro-6-methylphenoxy)-7-(1-ethylpropyl)-1-methyl-1H-benzimidazol-4-yl]methyl}-N-methylethanamine

HRID 1698596노트

반응식

HRID 1698596 반응식
[Cl:1][C:2]1[CH:25]=[C:24]([Cl:26])[CH:23]=[C:22]([CH3:27])[C:3]=1[O:4][C:5]1[N:9]([CH3:10])[C:8]2[C:11]([CH:17]([CH2:20][CH3:21])[CH2:18][CH3:19])=[CH:12][CH:13]=[C:14]([CH:15]=O)[C:7]=2[N:6]=1.[CH3:28][NH2:29].[C:30](O)(=O)[CH3:31].C(O[BH-](OC(=O)C)OC(=O)C)(=O)C.[Na+]>C(=O)(O)[O-].[Na+].C(OCC)(=O)C>[Cl:1][C:2]1[CH:25]=[C:24]([Cl:26])[CH:23]=[C:22]([CH3:27])[C:3]=1[O:4][C:5]1[N:9]([CH3:10])[C:8]2[C:11]([CH:17]([CH2:20][CH3:21])[CH2:18][CH3:19])=[CH:12][CH:13]=[C:14]([CH2:15][N:29]([CH3:28])[CH2:30][CH3:31])[C:7]=2[N:6]=1

참가 물질

7

실험 절차

To a mixture of 2-(2,4-dichloro-6-methylphenoxy)-7-(1-ethylpropyl)-1-methyl-1H-benzimidazole-4-carbaldehyde (120 mg, 0.296 mmol), methyl amine (2M tetrahydrofuran solution, 1.48 ml, 2.96 mmol), acetic acid (0.5 ml) and ethyl acetate (2.0 ml) was added sodium triacetoxyborohydride (314 mg, 1.48 mmol) and the reaction mixture was stirred at room temperature for 48 h. The residue was diluted with aqueous saturated sodium bicarbonate and extracted with ethyl acetate. The extracts were washed with water, dried over magnesium sulfate and concentrated in vacuo. The residue was purified by chromatography on alumina with a 5% ethyl acetate/n-hexane to give 93 mg (0.21 mmol, 70%) of the title compound as a white powder.

후처리

  1. extractionextracted with ethyl acetate
  2. washThe extracts were washed with water
  3. dry with materialdried over magnesium sulfate
  4. concentrationconcentrated in vacuo
  5. customThe residue was purified by chromatography on alumina with a 5% ethyl acetate/n-hexane

출처 및 근거

ORD 기록
ord-55975ab50cd84e3ba97d5118720814af
출처 데이터셋
uspto-grants-2012_04
특허 번호
US08163935B2

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