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Acetone → 4-fluoro-1H-indazol-3-amine

HRID 1874679
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HRID 1874679 반응식
F[C:2]1[CH:9]=[CH:8][CH:7]=[C:6]([F:10])[C:3]=1[C:4]#[N:5].O.[NH2:12][NH2:13].CC(C)=O>C(O)C>[F:10][C:6]1[CH:7]=[CH:8][CH:9]=[C:2]2[C:3]=1[C:4]([NH2:5])=[N:12][NH:13]2
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참가 물질

5

반응물 3

HCID 180AcetoneHCID 24654Hydrazine hydrate (1:1)HCID 746952,6-Difluorobenzonitrile

생성물 1

HCID 8179114-fluoro-1H-indazol-3-amine수율 140.3%

시약·촉매·용매 1

HCID 702Ethanol용매

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온도
90 °C

실험 절차

To a solution of 2,6-difluorobenzonitrile (3 g, 21.6 mmol) in anhydrous ethanol (50 mL) was added hydrazine hydrate (4.18 mL, 86 mmol). The reaction was heated at 90° C. under nitrogen for 4 hours. Reaction mixture was cooled to room temperature, treated with acetone (20 mL) and left to stand for 18 hours. The mixture was evaporated in-vacuo to yield an orange/brown solid which was partitioned between saturated aqueous sodium hydrogen carbonate solution and dichloromethane. The organic layer was passed through a hydrophobic frit and evaporated in-vacuo to yield a brown solid (4.58 g), which was absorbed onto Florisil (60-100 mesh), applied to a 100 g silica SPE cartridge and purified on a Flashmaster II using a 0-10% methanol in dichloromethane gradient over 60 min. Fractions 48-57 were combined and the solvent was evaporated in-vacuo to yield the title compound as a brown solid (3.08 g, 94%). LCMS (System B) RT=1.38 min, ES+ve m/z 152 (M+H)+.

후처리

  1. customReaction mixture
  2. temperaturewas cooled to room temperature
  3. waitleft
  4. customThe mixture was evaporated in-vacuo
  5. customto yield an orange/brown solid which
  6. customwas partitioned between saturated aqueous sodium hydrogen carbonate solution and dichloromethane
  7. customevaporated in-vacuo

출처 및 근거

ORD 기록
ord-b44b186572fd4f579748f38496ee708c
출처 데이터셋
uspto-grants-2012_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08304446B2

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