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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Acetic acid, [(4-fluoro-2-nitrophenyl)amino]oxo-, ethyl ester → 7-fluoro-1-hydroxyquinoxaline-2,3-(1H,4H)-dione

HRID 1974477
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HRID 1974477 반응식
[C:1]([NH:8][C:9]1[CH:14]=[CH:13][C:12]([F:15])=[CH:11][C:10]=1[N+:16]([O-:18])=O)([C:3](OCC)=[O:4])=[O:2]>[Pd].CN(C=O)C>[F:15][C:12]1[CH:11]=[C:10]2[C:9]([NH:8][C:1](=[O:2])[C:3](=[O:4])[N:16]2[OH:18])=[CH:14][CH:13]=1
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참가 물질

4

반응물 1

HCID 10658712Acetic acid, [(4-fluoro-2-nitrophenyl)amino]oxo-, ethyl ester

생성물 1

HCID 106317237-fluoro-1-hydroxyquinoxaline-2,3-(1H,4H)-dione수율 85.8%

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 6228Dimethylformamide용매

실험 절차

To a mixture of 5.6 g of 2-ethoxalylamino-5-fluoronitrobenzene and 170 ml of DMF was added 0.3 g of 10% Pd-C, and hydrogenation reaction was carried out at ordinary temperature and pressure. The reaction mixture was then filtered and concentrated under reduced pressure. The resulting residue was recrystallized from ethanol to provide 3.68 g (85%) of 7-fluoro-1-hydroxyquinoxaline-2,3-(1H,4H)-dione

후처리

  1. additionwas added
  2. filtrationThe reaction mixture was then filtered
  3. concentrationconcentrated under reduced pressure
  4. customThe resulting residue was recrystallized from ethanol

출처 및 근거

ORD 기록
ord-068db328e3d749cb93d3bc464b49f557
출처 데이터셋
uspto-grants-1994_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05283244

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