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Sodium Hydroxide → HCID 70665037, 화합물

HRID 1854537
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HRID 1854537 반응식
C([O:3][C:4]([C:6]1[CH:10]=[C:9]([NH:11][CH2:12][C:13](=[O:18])[C:14]([CH3:17])([CH3:16])[CH3:15])[N:8]([C:19]2[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=2)[N:7]=1)=[O:5])C.[OH-].[Na+]>C(O)C>[CH3:15][C:14]([CH3:17])([CH3:16])[C:13](=[O:18])[CH2:12][NH:11][C:9]1[N:8]([C:19]2[CH:20]=[CH:21][CH:22]=[CH:23][CH:24]=2)[N:7]=[C:6]([C:4]([OH:5])=[O:3])[CH:10]=1
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참가 물질

4

반응물 2

HCID 14798Sodium HydroxideHCID 706653315-(3,3-Dimethyl-2-oxo-butylamino)-1-phenyl-1H-pyrazole-3-carboxylic acid ethyl ester

생성물 1

HCID 70665037HCID 70665037, 화합물수율 82%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

2 g (6.07 mmol) of 5-(3,3-Dimethyl-2-oxo-butylamino)-1-phenyl-1H-pyrazole-3-carboxylic acid ethyl ester are dissolved in 15 ml ethanol, 12.1 ml (12.1 mmol, 2 eq) 1N NaOH are added and the resulting mixture is stirred overnight at RT. After evaporation of the solvent the residue is taken up in a mixture of 10 ml CH2Cl2 and 10 ml 0.1N HCl, the organic phase is separated, dried over Na2SO4 and the solvent removed in vacuo to obtain 5-(3,3-Dimethyl-2-oxo-butylamino)-1-phenyl-1H-pyrazole-3-carboxylic acid in a yield of 82% (1.5 g)

후처리

  1. customAfter evaporation of the solvent the residue
  2. additionis taken up in a mixture of 10 ml CH2Cl2 and 10 ml 0.1N HCl
  3. customthe organic phase is separated
  4. dry with materialdried over Na2SO4
  5. customthe solvent removed in vacuo

출처 및 근거

ORD 기록
ord-e025a5d9ebab4a279292b13b8f514840
출처 데이터셋
uspto-grants-2015_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08962671B2

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