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

HRID 1068611
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Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1068611
[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
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 2

HCID 61436Stannous chloride dihydrateHCID 15194586HCID 15194586, Verbindung

Produkt 1

HCID 100604066-Bromo-7-fluoro-3,4-dihydroquinoxalin-2(1H)-one

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 702EthanolLösungsmittel

Versuchsvorschrift

A solution of 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 NaSO4 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): δ 3.684 (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).

Aufarbeitung

  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 NaSO4
  5. customremoved under vacuum
  6. customto yield 0.241 g (64%

Quellen und Nachweise

ORD-Eintrag
ord-df697c7578b34769afe1147c9ed2c1de
Quelldatensatz
uspto-grants-2001_06
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US06251903B1

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