Acetic Acid → 3-tert-butyl-1-(4-nitrophenyl)-1H-pyrazol-5-amine

HRID 221858

반응식

HRID 221858 반응식
[CH3:1][C:2]([CH3:9])([CH3:8])[C:3](=O)[CH2:4][C:5]#[N:6].[N+:10]([C:13]1[CH:18]=[CH:17][C:16]([NH:19][NH2:20])=[CH:15][CH:14]=1)([O-:12])=[O:11].C(O)(=O)C>CCO>[C:2]([C:3]1[CH:4]=[C:5]([NH2:6])[N:19]([C:16]2[CH:15]=[CH:14][C:13]([N+:10]([O-:12])=[O:11])=[CH:18][CH:17]=2)[N:20]=1)([CH3:9])([CH3:8])[CH3:1]

참가 물질

5

반응물 3

HCID 176Acetic AcidHCID 108871Pentanenitrile, 4,4-dimethyl-3-oxo-HCID 3310889(4-Nitrophenyl)hydrazine

생성물 1

HCID 13023603-tert-butyl-1-(4-nitrophenyl)-1H-pyrazol-5-amine수율 85%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

To a solution of 4,4-dimethyl-3-oxopentanenitrile (20.4 g, 163 mmol) and 4-nitrophenylhydrazine (25.0 g, 163 mmol) in anhydrous EtOH (300 mL) was added acetic acid (3.4 mL, 60 mL) dropwise. The reaction was stirred at reflux under N2 for 18 h. The reaction mixture was cooled to room temperature and concentrated at reduced pressure. The residue was partitioned between EtOAc (500 mL) and aqueous saturated NaHCO3 solution (300 mL). The organic layer was washed with water and brine, dried over Na2SO4, and concentrated at reduced pressure. The crude residue was purified by MPLC (eluting with 80:20 hexanes/EtOAc) to give 36.0 g (85%) of the desired product. 1H-NMR (DMSO-d6) δ 8.28 (d, J=6.9 Hz, 2H), 7.93 (d, J=6.9 Hz, 2H), 5.55 (s, 2H), 5.46 (s, 1H), 1.20 (s, 9H); MS LC-MS [M+H]+=261, RT=2.74 min.

후처리

  1. temperatureat reflux under N2 for 18 h
  2. concentrationconcentrated at reduced pressure
  3. customThe residue was partitioned between EtOAc (500 mL) and aqueous saturated NaHCO3 solution (300 mL)
  4. washThe organic layer was washed with water and brine
  5. dry with materialdried over Na2SO4
  6. concentrationconcentrated at reduced pressure
  7. customThe crude residue was purified by MPLC (eluting with 80:20 hexanes/EtOAc)

출처 및 근거

ORD 기록
ord-f0b1327c3d89499fa6b24faabbe4aacf
출처 데이터셋
uspto-grants-2012_06
특허 번호
US08207166B2

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