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Pyruvic Acid → 1-ethyl-3-methylquinoxalin-2(1H)-one

HRID 1961564
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HRID 1961564 반응식
[CH2:1]([NH:3][C:4]1[C:5]([NH2:10])=[CH:6][CH:7]=[CH:8][CH:9]=1)[CH3:2].O=[C:12]([CH3:16])[C:13](O)=[O:14]>CO>[CH2:1]([N:3]1[C:4]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[N:10]=[C:12]([CH3:16])[C:13]1=[O:14])[CH3:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 1060Pyruvic AcidHCID 902751,2-Benzenediamine, N1-ethyl-

생성물 1

HCID 129004081-ethyl-3-methylquinoxalin-2(1H)-one수율 56%

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

5,4 g (39,6 mM) of N-ethylbenzene-1,2-diamine and 2,76 ml (39,6 mM) of 2-oxopropanoic acid in 200 ml of methanol were refluxed for 8 h. The solvent was removed under vacuum. The residue was further purified by silica gel column chromatography, using dichloromethane, followed by dichloromethane/dimethylketone (95/5) as eluant to give 4,2 g of 1-ethyl-3-methyl-quinoxalin-2(1H)-one as a yellow solid. Yield: 56,7%.

후처리

  1. customThe solvent was removed under vacuum
  2. customThe residue was further purified by silica gel column chromatography

출처 및 근거

ORD 기록
ord-078867f2ff1d426a9bbd7a135c45bc2b
출처 데이터셋
uspto-grants-2013_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08415352B2

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