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N-bromobutanimide → 5-Bromo-3-(3-methylpyridazin-4-yloxy)pyridin-2-amine

HRID 1809646
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인쇄 미리보기

반응식

HRID 1809646 반응식
[CH3:1][C:2]1[N:3]=[N:4][CH:5]=[CH:6][C:7]=1[O:8][C:9]1[C:10]([NH2:15])=[N:11][CH:12]=[CH:13][CH:14]=1.[Br:16]N1C(=O)CCC1=O>CN(C=O)C.O>[Br:16][C:13]1[CH:14]=[C:9]([O:8][C:7]2[CH:6]=[CH:5][N:4]=[N:3][C:2]=2[CH3:1])[C:10]([NH2:15])=[N:11][CH:12]=1
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참가 물질

5

반응물 2

HCID 67184N-bromobutanimideHCID 674859363-(3-Methylpyridazin-4-yloxy)pyridin-2-amine

생성물 1

HCID 674853455-Bromo-3-(3-methylpyridazin-4-yloxy)pyridin-2-amine수율 95%

시약·촉매·용매 2

HCID 962Water용매HCID 6228Dimethylformamide용매

실험 절차

3-(3-Methylpyridazin-4-yloxy)pyridin-2-amine (0.50 g, 2.5 mmol) was dissolved in DMF (7 mL). N-Bromosuccinimide (0.46 g, 2.6 mmol) was added and the solution stirred at ambient temperature for 5 minutes. The solution was diluted with water and filtered through celite (rinsing with chloroform). The solution was extracted with chloroform, dried (Na2SO4), filtered and concentrated. Flash chromatography gave 5-bromo-3-(3-methylpyridazin-4-yloxy)pyridin-2-amine (0.66 g, 95%).

후처리

  1. filtrationfiltered through celite (rinsing with chloroform)
  2. extractionThe solution was extracted with chloroform
  3. dry with materialdried (Na2SO4)
  4. filtrationfiltered
  5. concentrationconcentrated

출처 및 근거

ORD 기록
ord-4f16f41b768c4d76a78711125687c369
출처 데이터셋
uspto-grants-2013_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08362037B2

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