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Nitric Acid → 5-bromo-4-fluoro-3-nitro-1H-pyrrolo[2,3-b]pyridine

HRID 79612
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HRID 79612 반응식
[Br:1][C:2]1[C:3]([F:11])=[C:4]2[CH:10]=[CH:9][NH:8][C:5]2=[N:6][CH:7]=1.[N+:12]([O-])([OH:14])=[O:13]>O>[Br:1][C:2]1[C:3]([F:11])=[C:4]2[C:10]([N+:12]([O-:14])=[O:13])=[CH:9][NH:8][C:5]2=[N:6][CH:7]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 944Nitric AcidHCID 534129385-bromo-4-fluoro-1H-pyrrolo[2,3-b]pyridine

생성물 1

HCID 602052755-bromo-4-fluoro-3-nitro-1H-pyrrolo[2,3-b]pyridine수율 86.8%

시약·촉매·용매 1

HCID 962Water용매

실험 절차

5-Bromo-4-fluoro-1H-pyrrolo[2,3-b]pyridine (0.100 g, 0.465 mmol, see Example 51) was added slowly to fuming HNO3 (5 mL) at 0° C. and stirred for 10 minutes. Ice was then added, followed by the addition of water. The resulting solid product was then filtered, and washed with water and dried to give 5-bromo-4-fluoro-3-nitro-1H-pyrrolo[2,3-b]pyridine (0.105 g, 86.8% yield).

후처리

  1. additionIce was then added
  2. filtrationThe resulting solid product was then filtered
  3. washwashed with water
  4. customdried

출처 및 근거

ORD 기록
ord-13fe756dd6144800b6353bd8783effc1
출처 데이터셋
uspto-grants-2014_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08841304B2

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