Reaktionsgleichung
[H-].[Na+].N1[C:12]2[C:7](=C[CH:9]=[CH:10][CH:11]=2)[NH:6][C:5](=[O:13])C1=O.[CH3:15]I.O.[CH3:18][N:19]([CH:21]=[O:22])[CH3:20]>>[CH3:18][N:19]1[C:20]2[C:7](=[CH:12][CH:11]=[CH:10][CH:9]=2)[N:6]([CH3:15])[C:5](=[O:13])[C:21]1=[O:22]Komponenten
6
Versuchsvorschrift
To a solution of NaH (2.5 g) in DMF (200 mL) was added quinoxaline-2,3(1H,4H)-dione (5 g) in portions, followed by the slow addition of methyl iodide (3.8 mL). The reaction mixture was stirred at ambient temperature for 4 hours, then water was added (200 mL) The resulting precipitate was collected by filtration and washed with water to afford 1,4-dimethylquinoxaline-2,3(1H,4H)-dione as a white solid in 95% yield. 1H NMR (400 MHz, DMSO-d6): δ, ppm: 3.50 (s, 6H), 7.25 (m, 2H), 7.38 (m, 4H).
Aufarbeitung
- filtrationwas collected by filtration
- washwashed with water
Quellen und Nachweise
- ORD-Eintrag
- ord-de036f45e6f94576b5b625da91cf23fc
- Quelldatensatz
- uspto-grants-2011_05
- Patentnummer
- US07939671B2
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