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Water → HCID 18316650, 화합물

HRID 275796
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HRID 275796 반응식
[H-].[Na+].[Br:3][C:4]1[C:12]2[NH:11][C:10]([C:13]([F:16])([F:15])[F:14])=[N:9][C:8]=2[C:7]([O:17][CH3:18])=[CH:6][CH:5]=1.[CH3:19][O:20][C:21]1[CH:28]=[CH:27][C:24]([CH2:25]Cl)=[CH:23][CH:22]=1.O>CN(C)C=O.[I-].C([N+](CCCC)(CCCC)CCCC)CCC>[Br:3][C:4]1[C:12]2[N:11]([CH2:25][C:24]3[CH:27]=[CH:28][C:21]([O:20][CH3:19])=[CH:22][CH:23]=3)[C:10]([C:13]([F:14])([F:15])[F:16])=[N:9][C:8]=2[C:7]([O:17][CH3:18])=[CH:6][CH:5]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

7

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HCID 962WaterHCID 24758Sodium hydrideHCID 699934-Methyloxybenzyl chlorideHCID 178488288HCID 178488288, 화합물

생성물 1

HCID 18316650HCID 18316650, 화합물

시약·촉매·용매 2

HCID 67553Tetrabutylammonium Iodide촉매
HCID 6228
Dimethylformamide
용매

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온도
90 °C

실험 절차

Sodium hydride (0.16 g; 60% dispersion in oil) was added to a solution of 4-bromo-7-methoxy-2-trifluoromethylbenzimidazole (1.0 g) in N,N-dimethylformamide (20 ml). The mixture was stirred at room temperature for 10 minutes before addition of 4-methoxybenzyl chloride (0.56 ml) and catalytic tetrabutylammonium iodide. The reaction was heated at 90° C. for 6 h, then poured into water (100 ml) and extracted with ethyl acetate (2×100 ml). The combined organic phases were washed with water (100 ml) and brine (50 ml), dried over magnesium sulphate, evaporated in vacuo and purified by flash chromatography eluting with 33% ethyl acetate in hexane to afford the title compound as a white solid (0.52 g).

후처리

  1. extractionextracted with ethyl acetate (2×100 ml)
  2. washThe combined organic phases were washed with water (100 ml) and brine (50 ml)
  3. dry with materialdried over magnesium sulphate
  4. customevaporated in vacuo
  5. custompurified by flash chromatography
  6. washeluting with 33% ethyl acetate in hexane

출처 및 근거

ORD 기록
ord-4d63fe54143147838040276999e60fed
출처 데이터셋
uspto-grants-2002_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06353010B1

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