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Benzimidazole → HCID 59375036, 화합물

HRID 661868
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HRID 661868 반응식
[Br:1][C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([CH2:8]Br)[C:3]=1[CH3:10].[NH:11]1[C:15]2[CH:16]=[CH:17][CH:18]=[CH:19][C:14]=2[N:13]=[CH:12]1.C(=O)([O-])[O-].[K+].[K+]>C(#N)C.CCOC(C)=O>[Br:1][C:2]1[C:3]([CH3:10])=[C:4]([CH:5]=[CH:6][CH:7]=1)[CH2:8][N:11]1[C:15]2[CH:16]=[CH:17][CH:18]=[CH:19][C:14]=2[N:13]=[CH:12]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 5798BenzimidazoleHCID 11430Potassium CarbonateHCID 226726481-Bromo-3-(bromomethyl)-2-methylbenzene

생성물 1

HCID 59375036HCID 59375036, 화합물수율 82%

시약·촉매·용매 2

HCID 6342Acetonitrile용매HCID 8857Ethyl Acetate용매

실험 절차

A mixture of 1-bromo-3-(bromomethyl)-2-methylbenzene (250 mg, 0.947 mmol), 1H-benzo[d]imidazole (336 mg, 2.84 mmol) and potassium carbonate (131 mg, 0.947 mmol) in acetonitrile (5 mL) was stirred at rt for 5 h, The mixture was diluted with EtOAc and filtered, and the solid was washed with EtOAc. The filtrate was washed with water, dried and concentrated. The residue was purified by column chromatography (eluting with a gradient from 60:40 hexane-EtOAc to EtOAc), to provide 1-(3-bromo-2-methylbenzyl)-1H-benzo[d]imidazole as a white solid (233 mg, 82%). 1H NMR (400 MHz, chloroform-d) δ 8.14 (1H, s), 7.68-7.78 (1H, m), 7.56 (1H, d, J=7.9 Hz), 7.36-7.44 (1H, m), 7.25-7.34 (2H, m), 7.03 (1H, t, J=7.8 Hz), 6.82 (1H, d, J=7.7 Hz), 5.58 (2H, s), 2.45 (3H, s). Mass spectrum m/z 301, 303 (M+H)+.

후처리

  1. filtrationfiltered
  2. washthe solid was washed with EtOAc
  3. washThe filtrate was washed with water
  4. customdried
  5. concentrationconcentrated
  6. customThe residue was purified by column chromatography (
  7. washeluting with a gradient from 60:40 hexane-EtOAc to EtOAc),

출처 및 근거

ORD 기록
ord-77e6773f6bfe4097877a5213ce1d2875
출처 데이터셋
uspto-grants-2011_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08084620B2

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