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Ethanol → 2-(5-amino-1-p-tolyl-1H-pyrazol-3-yl)-2-methylpropan-1-ol

HRID 220215
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인쇄 미리보기

반응식

HRID 220215 반응식
[OH:1][CH2:2][C:3]([CH3:10])([CH3:9])[C:4](=O)[CH2:5][C:6]#[N:7].Cl[NH:12][NH:13][C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1.[CH2:20](O)C>>[NH2:7][C:6]1[N:13]([C:14]2[CH:19]=[CH:18][C:17]([CH3:20])=[CH:16][CH:15]=2)[N:12]=[C:4]([C:3]([CH3:10])([CH3:9])[CH2:2][OH:1])[CH:5]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 702EthanolHCID 120447945-Hydroxy-4,4-dimethyl-3-oxopentanenitrileHCID 205084581-Chloro-2-phenylhydrazine

생성물 1

HCID 111183102-(5-amino-1-p-tolyl-1H-pyrazol-3-yl)-2-methylpropan-1-ol

반응 조건

온도
90 °C

실험 절차

5-hydroxy-4,4-dimethyl-3-oxopentanenitrile (0.32 g, 2.27 mmol) and 1-chloro-2-phenylhydrazine (0.361 g, 2.49 mmol) were combined in ethanol and heated at 90° C. for 8 hours. The reaction was cooled and concentrated, and the residue was triturated with ethyl acetate. The solids were collected by filtration, triturated with acetone and rinsed to isolate 36 mg of the title compound as a pure white solid. MS M+1(246).

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후처리

  1. temperatureThe reaction was cooled
  2. concentrationconcentrated
  3. customthe residue was triturated with ethyl acetate
  4. filtrationThe solids were collected by filtration
  5. customtriturated with acetone
  6. washrinsed

출처 및 근거

ORD 기록
ord-728472c4e07a41d58017348cafe6c70c
출처 데이터셋
uspto-grants-2012_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08202899B2

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