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Hydrazine hydrate (1:1) → 5-Bromo-7-fluoro-1H-indazole

HRID 1057133
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HRID 1057133 반응식
CO/[N:3]=[CH:4]/[C:5]1[CH:10]=[C:9]([Br:11])[CH:8]=[C:7]([F:12])[C:6]=1F.O.[NH2:15]N>C1COCC1>[Br:11][C:9]1[CH:10]=[C:5]2[C:6](=[C:7]([F:12])[CH:8]=1)[NH:15][N:3]=[CH:4]2
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참가 물질

4

반응물 2

HCID 24654Hydrazine hydrate (1:1)HCID 87153195O-Methyl-(E)-5-bromo-2,3-difluorobenzaldehyde oxime

생성물 1

HCID 667931105-Bromo-7-fluoro-1H-indazole

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

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온도
90 °C

실험 절차

A mixture of (E)-5-bromo-2,3-difluorobenzaldehyde O-methyl oxime (19.65 g, 78.6 mmol), hydrazine hydrate (80 mL), and dry THF (80 mL), was heated at 90° C. for 84 h. Work-up: the organic solvent was evaporated. The resulting mixture was diluted with EtOAc (400 mL), washed with water (150 mL), dried over Na2SO4, and concentrated in vacuo. The residue was purified by column chromatography on silica gel (0˜20% EtOAc in petroleum ether) to give 5-bromo-7-fluoro-1H-indazole as a white solid (9.3 g). 1H NMR (300 MHz, CDCl3): δ 13.83 (br, 1H), 8.16 (s, 1H), 7.87 (s, 1H), 7.45 (d, 1H).

후처리

  1. customthe organic solvent was evaporated
  2. additionThe resulting mixture was diluted with EtOAc (400 mL)
  3. washwashed with water (150 mL)
  4. dry with materialdried over Na2SO4
  5. concentrationconcentrated in vacuo
  6. customThe residue was purified by column chromatography on silica gel (0˜20% EtOAc in petroleum ether)

출처 및 근거

ORD 기록
ord-74ab2c47575147669173fc18ef7dedfc
출처 데이터셋
uspto-grants-2016_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09399646B2

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