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Dimethylformamide → 3-Azido-6-fluoro-1,3,4,5-tetrahydro-2H-1-benzazepin-2-one

HRID 2035698
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HRID 2035698 반응식
CN(C=O)C.[F:6][C:7]1[C:12]2[CH2:13][CH2:14][CH:15](I)[C:16](=[O:18])[NH:17][C:11]=2[CH:10]=[CH:9][CH:8]=1.[N-:20]=[N+:21]=[N-:22].[Na+]>O>[N:20]([CH:15]1[CH2:14][CH2:13][C:12]2[C:7]([F:6])=[CH:8][CH:9]=[CH:10][C:11]=2[NH:17][C:16]1=[O:18])=[N+:21]=[N-:22]
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참가 물질

5

반응물 3

HCID 6228DimethylformamideHCID 33557Sodium AzideHCID 541183906-Fluoro-3-iodo-4,5-dihydro-1H-benzo[b]azepin-2(3H)-one

생성물 1

HCID 190256673-Azido-6-fluoro-1,3,4,5-tetrahydro-2H-1-benzazepin-2-one

시약·촉매·용매 1

HCID 962Water용매

실험 절차

DMF (300 ml) was added to a mixture of 6-fluoro-3-iodo-1,3,4,5-tetrahydro-1-benzazepin-2-one (42.5 g) and sodium azide (13.59 g, 209 mmol) at room temperature and the reaction was stirred overnight. The mixture was diluted with water (2000 mL) and a precipitate formed, which was filtered off and washed with water. The precipitate was taken up in dichloromethane and washed with brine, dried over Na2SO4, filtered, and concentrated. The crude 3-Azido-6-fluoro-1,3,4,5-tetrahydro-1-benzazepin-2-one was isolated as a dark brown solid. Residual DMF remains in the sample, which was used without further manipulation in the next reaction.

후처리

  1. customa precipitate formed
  2. filtrationwhich was filtered off
  3. washwashed with water
  4. washwashed with brine
  5. dry with materialdried over Na2SO4
  6. filtrationfiltered
  7. concentrationconcentrated

출처 및 근거

ORD 기록
ord-02df447e8eb34b6b8b9cb962fe70024a
출처 데이터셋
uspto-grants-2013_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08575150B2

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