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

HRID 1918161노트

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HRID 1918161 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-f619103aeb8f48e29292d61611a26cdf
출처 데이터셋
uspto-grants-2013_12
특허 번호
US08618289B2

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