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2-(3,5-dimethyl-4-nitro-1H-pyrazol-1-yl)ethanol → HCID 28492268, 화합물

HRID 624067
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HRID 624067 반응식
[CH3:1][C:2]1[C:6]([N+:7]([O-])=O)=[C:5]([CH3:10])[N:4]([CH2:11][CH2:12][OH:13])[N:3]=1>CCOC(C)=O.CCO.O=[Pt]=O>[NH2:7][C:6]1[C:2]([CH3:1])=[N:3][N:4]([CH2:11][CH2:12][OH:13])[C:5]=1[CH3:10]
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참가 물질

5

반응물 1

HCID 196169562-(3,5-dimethyl-4-nitro-1H-pyrazol-1-yl)ethanol

생성물 1

HCID 28492268HCID 28492268, 화합물

시약·촉매·용매 3

HCID 345198Adams' catalyst촉매HCID 702Ethanol용매2회HCID 8857Ethyl Acetate용매

실험 절차

To a solution of 2-(3,5-dimethyl-4-nitro-1H-pyrazol-1-yl)ethanol (624 mg, 3.37 mmol) in EtOAc (1.2 mL, degassed) and EtOH (3.6 mL, degassed), PtO2 (66 mg, 0.34 mmol) was added and the reaction mixture was stirred at rt under a H2-atmosphere for 30 h. The mixture was diluted with EtOH, filtered over celite and the filter cake was rinsed with EtOH. The filtrate was concentrated to obtain 2-(4-amino-3,5-dimethyl-1H-pyrazol-1-yl)ethanol as a pale brown solid, which was used in the next step without further purification. LC-MS conditions A: tR=0.16 min, [M+H]+=156.29.

후처리

  1. filtrationfiltered over celite
  2. washthe filter cake was rinsed with EtOH
  3. concentrationThe filtrate was concentrated

출처 및 근거

ORD 기록
ord-64b539c5722544fe886d95e3c08f3fba
출처 데이터셋
uspto-grants-2016_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09303023B2

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