Reaktion #1699

ord-d0f3e38e8aab4374bc8286880e180242

Reaktionsgleichung

CC(=O)[O-].[NH4+]
ammonium acetate
CCOC(=O)c1cn(C2Cc3ccccc3C2=O)c(C(=O)OCC)n1
diethyl 1-(1-oxoindan-2-yl)imidazole-2,4-dicarboxylate
CCOC(=O)c1cn2c3c([nH]c(=O)c2n1)-c1ccccc1C3
ethyl 4,5-dihydro-4-oxo-10H-imidazol[1,2-a]indeno[1,2-e]pyrazine-2-carboxylate
Ausbeute 37.7%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturthe mixture is heated
  2. 2
    Temperaturto reflux for 2 hours
  3. 3
    TemperaturAfter cooling to a temperature
  4. 4
    Sonstigeclose to 20° C. the precipitate
  5. 5
    Sonstigeformed
  6. 6
    Filtrationis filtered off
  7. 7
    Waschenrinsed with distilled water

Vorschrift

51.2 g of ammonium acetate are added in small portions to a solution of 2 g of diethyl 1-(1-oxoindan-2-yl)imidazole-2,4-dicarboxylate in 80 ml of acetic acid and the mixture is heated to reflux for 2 hours. After cooling to a temperature close to 20° C. the precipitate formed is filtered off and rinsed with distilled water and then with methyl ethyl ketone (2×10 ml) to give 0.65 g of ethyl 4,5-dihydro-4-oxo-10H-imidazol[1,2-a]indeno[1,2-e]pyrazine-2-carboxylate in the form of a beige solid melting above 260° C. (analysis % calculated C: 65.08, H: 4.44, N: 14.23; % found C: 65.2, H: 4.3, N: 13.8).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05726175uspto-grants-1998_03