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Dimethylformamide → 4-(4-fluoro-phenoxy)-2-methylsulfanyl-6-(pyridin-3-yloxy)-1H-benzimidazole

HRID 13253
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HRID 13253 반응식
[C:1](=O)([O-])[O-].[K+].[K+].CI.CN(C)C=O.[F:14][C:15]1[CH:38]=[CH:37][C:18]([O:19][C:20]2[C:28]3[N:27]=[C:26]([SH:29])[NH:25][C:24]=3[CH:23]=[C:22]([O:30][C:31]3[CH:32]=[N:33][CH:34]=[CH:35][CH:36]=3)[CH:21]=2)=[CH:17][CH:16]=1>C(OCC)(=O)C>[F:14][C:15]1[CH:38]=[CH:37][C:18]([O:19][C:20]2[C:28]3[N:27]=[C:26]([S:29][CH3:1])[NH:25][C:24]=3[CH:23]=[C:22]([O:30][C:31]3[CH:32]=[N:33][CH:34]=[CH:35][CH:36]=3)[CH:21]=2)=[CH:17][CH:16]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 6228DimethylformamideHCID 6328Methyl iodideHCID 11430Potassium CarbonateHCID 178505885HCID 178505885, 화합물

생성물 1

HCID 231455514-(4-fluoro-phenoxy)-2-methylsulfanyl-6-(pyridin-3-yloxy)-1H-benzimidazole

시약·촉매·용매 1

HCID 8857Ethyl Acetate용매

반응 조건

온도
0 °C

실험 절차

30 mg of potassium carbonate and 0.014 ml of methyl iodide were added to a dimethylformamide (1.0 ml) solution of 78 mg of 4-(4-fluoro-phenoxy)-6-(pyridin-3-yloxy)-1H-benzimidazole-2-thiol produced in Example 115, and the reaction liquid was stirred at 0° C. for 30 minutes. The reaction liquid was diluted with ethyl acetate, washed with water and saturated saline in order, and dried with anhydrous magnesium sulfate. The solvent was evaporated away under reduced pressure to obtain the entitled compound.

후처리

  1. customthe reaction liquid
  2. customThe reaction liquid
  3. washwashed with water and saturated saline in order
  4. dry with materialdried with anhydrous magnesium sulfate
  5. customThe solvent was evaporated away under reduced pressure
  6. customto obtain the entitled compound

출처 및 근거

ORD 기록
ord-f463d4d7b402488a8b1556f973370678
출처 데이터셋
uspto-grants-2010_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07728025B2

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