Phenylhydrazine hydrochloride → 3-(1,1-difluoroethyl)-1-phenyl-1H-pyrazol-5-amine

HRID 1918113노트

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HRID 1918113 반응식
[F:1][C:2]([F:9])([CH3:8])[C:3](=O)[CH2:4][C:5]#[N:6].Cl.[C:11]1([NH:17][NH2:18])[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1>C(O)C>[F:1][C:2]([C:3]1[CH:4]=[C:5]([NH2:6])[N:17]([C:11]2[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=2)[N:18]=1)([F:9])[CH3:8]

참가 물질

4

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온도
70 °C

실험 절차

A stirred mixture of 4,4-difluoro-3-oxopentanenitrile (prepared as described in Example 152A Step 1) (1 g, 7.52 mmol) and phenyl hydrazine hydrochloride (1.08 g, 7.52 mmol) in ethanol (30 mL) was heated at 70° C. for 8 h. After cooling to rt, the mixture was concentrated under reduced pressure. The residue was partitioned between dichloromethane (200 mL) and saturated aqueous sodium hydrogen carbonate solution (200 mL). The organic layer was separated and dried over magnesium sulfate and filtered. Concentration under reduced pressure gave an oil, which was purified via silica gel column chromatography (eluting with a gradient of 5% to 65% ethyl acetate in hexanes) to afford 3-(1,1-difluoroethyl)-1-phenyl-1H-pyrazol-5-amine (528 mg, 31%) as a yellow oil. 1H NMR (300 MHz, CDCl3) δ 7.36-7.57 (m, 5H), 5.81 (s, 1H), 3.84 (brs, 2H), 2.01 (t, J=18 Hz, 3H); LC-MS (ESI) m/z 224 (M+H)+.

후처리

  1. temperatureAfter cooling to rt
  2. concentrationthe mixture was concentrated under reduced pressure
  3. customThe residue was partitioned between dichloromethane (200 mL) and saturated aqueous sodium hydrogen carbonate solution (200 mL)
  4. customThe organic layer was separated
  5. dry with materialdried over magnesium sulfate
  6. filtrationfiltered
  7. concentrationConcentration under reduced pressure
  8. customgave an oil, which
  9. customwas purified via silica gel column chromatography (
  10. washeluting with a gradient of 5% to 65% ethyl acetate in hexanes)

출처 및 근거

ORD 기록
ord-dc6c821a1abe4ebdb5a73e1621d03574
출처 데이터셋
uspto-grants-2013_12
특허 번호
US08618289B2

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