Reaktionsgleichung
C[O:2][C:3](=O)[CH2:4][C:5]1[C:9]2[CH:10]=[C:11]([CH2:14][N:15]([CH3:17])[CH3:16])[CH:12]=[CH:13][C:8]=2[O:7][CH:6]=1.[NH3:19]>CO>[CH3:16][N:15]([CH2:14][C:11]1[CH:12]=[CH:13][C:8]2[O:7][CH:6]=[C:5]([CH2:4][C:3]([NH2:19])=[O:2])[C:9]=2[CH:10]=1)[CH3:17]Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Reaktionsbedingungen
- Temperatur
- 60 °C
Versuchsvorschrift
A solution of (5-dimethylaminomethyl-benzofuran-3-yl)-acetic acid methyl ester (170 mg, 0.69 mmol) in a mixture of methanol (15 mL) and liquid ammonia (15 mL) is stirred for 2 days in an autoclave at 60° C. After careful evaporation of the ammonia, the remaining solvent is evaporated in vacuo to afford the title compound as a yellow oil (160 mg, 0.69 mmol, 100%). MS (ES+): 233 (M(C13H16N2O2)+H)+.
Aufarbeitung
- customAfter careful evaporation of the ammonia
- customthe remaining solvent is evaporated in vacuo
Quellen und Nachweise
- ORD-Eintrag
- ord-c310eddfd65b492ca05842706b02d96f
- Quelldatensatz
- uspto-grants-2012_06
- Patentnummer
- US08193236B2
Verknüpfte Notizen
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