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Stannous chloride dihydrate → 6-Bromo-7-fluoro-3,4-dihydroquinoxalin-2(1H)-one

HRID 1781016
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HRID 1781016 반응식
[Na+].[Br:2][C:3]1[C:4]([F:17])=[CH:5][C:6]([N+:14]([O-])=O)=[C:7]([NH:9][CH2:10][C:11]([O-])=[O:12])[CH:8]=1.O.O.[Sn](Cl)Cl>C(O)C>[Br:2][C:3]1[CH:8]=[C:7]2[C:6](=[CH:5][C:4]=1[F:17])[NH:14][C:11](=[O:12])[CH2:10][NH:9]2
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 61436Stannous chloride dihydrateHCID 15194586HCID 15194586, 화합물

생성물 1

HCID 100604066-Bromo-7-fluoro-3,4-dihydroquinoxalin-2(1H)-one수율 64%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

N-(5'-bromo-4'-fluoro-2'-nitrophenyl)glycine sodium salt (0.450 g, 1.54 mmol, as prepared above) and tin (II) chloride dihydrate (1.039 g, 4.605 mmol, Aldrich, used as received) in ethanol (7.0 mL) was refluxed for 30 min. It was then cooled to room temperature and solvent was removed under vacuum. The residue was diluted with water (15.0 mL) and basified with 10% Na2CO3 to pH ~8. The resulting suspension was extracted with ethyl acetate (100 mL). The ethyl acetate was dried over anhydrous Na2SO4 and removed under vacuum to yield 0.241 g (64%) of the title compound as a yellow powder, m.p. 214°-216° C.; 1H NMR (DMSO-d6): δ3.684 (s, 2H), 6.062 (s, 1H), 6.631 (d, 1H, J=9.3 Hz), 6.825 (d, 1H, J=6.6 Hz), 10.303 (s, 1H).

후처리

  1. customsolvent was removed under vacuum
  2. additionThe residue was diluted with water (15.0 mL)
  3. extractionThe resulting suspension was extracted with ethyl acetate (100 mL)
  4. dry with materialThe ethyl acetate was dried over anhydrous Na2SO4
  5. customremoved under vacuum

출처 및 근거

ORD 기록
ord-15e37d10d88148d9bb4bb35e4f153e2c
출처 데이터셋
uspto-grants-1997_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05631373

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