Potassium Carbonate → phenyl 3-ethyl-1-phenyl-1H-pyrazol-5-ylcarbamate

HRID 631711노트

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HRID 631711 반응식
[CH2:1]([C:3]1[CH:7]=[C:6]([NH2:8])[N:5]([C:9]2[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=2)[N:4]=1)[CH3:2].C(=O)([O-])[O-].[K+].[K+].Cl[C:22]([O:24][C:25]1[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=1)=[O:23]>C1COCC1>[CH2:1]([C:3]1[CH:7]=[C:6]([NH:8][C:22](=[O:23])[O:24][C:25]2[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=2)[N:5]([C:9]2[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=2)[N:4]=1)[CH3:2]

참가 물질

5

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온도
-5 °C

실험 절차

To a stirred mixture of 3-ethyl-1-phenyl-1H-pyrazol-5-amine (1.00 g, 5.34 mmol) and potassium carbonate (1.48 g, 10.68 mmol) in THF (50 mL) at −5° C., was added phenyl chloroformate (1.00 g, 6.41 mmol) dropwise. After stirring for a further 30 min at −5° C., the reaction mixture it was warmed to rt and stirred for a further 15 h. The mixture was quenched with water and extracted with dichloromethane. The combined dichloromethane layers were dried over magnesium sulfate, concentrated under reduced pressure, and dried under vacuum to afford an oil. Recrystallization from petroleum ether gave phenyl 3-ethyl-1-phenyl-1H-pyrazol-5-ylcarbamate (1.00 g, 61%) as a colorless solid. 1H NMR (400 MHz, DMSO-d6) δ 10.07 (brs, 1H), 6.74-7.59 (m, 10H), 6.30 (s, 1H), 2.60 (q, J=7.6 Hz, 2H), 1.21 (t, J=7.6 Hz, 3H); LC-MS (ESI) m/z 308 (M+H)+.

후처리

  1. temperaturethe reaction mixture it was warmed to rt
  2. stirringstirred for a further 15 h
  3. customThe mixture was quenched with water
  4. extractionextracted with dichloromethane
  5. dry with materialThe combined dichloromethane layers were dried over magnesium sulfate
  6. concentrationconcentrated under reduced pressure
  7. customdried under vacuum
  8. customto afford an oil
  9. customRecrystallization from petroleum ether

출처 및 근거

ORD 기록
ord-35f1849fa93c4a38b621518df7c7bf40
출처 데이터셋
uspto-grants-2016_04
특허 번호
US09320739B2

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