Ammonia → 8-methoxy-3-phenyl-2,7-naphthyridin-1(2H)-one
Reaktionsgleichung
[CH3:1][O:2][C:3]1[N:12]=[CH:11][CH:10]=[C:9]([C:13]#[C:14][C:15]2[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=2)[C:4]=1[C:5](OC)=[O:6].[NH3:21]>CO>[CH3:1][O:2][C:3]1[N:12]=[CH:11][CH:10]=[C:9]2[C:4]=1[C:5](=[O:6])[NH:21][C:14]([C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1)=[CH:13]2Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Reaktionsbedingungen
- Temperatur
- 115 °C
Versuchsvorschrift
Methyl 2-methoxy-4-(phenylethynyl)nicotinate (100 mg, 0.37 mmol) is dissolved in 7% NH3 in MeOH (3 mL) and heated at 115° C. in a sealed tube for 24 hours. The reaction mixture is cooled to 0° C. and the cyclized product is crystallized out. The compound is collected by filtration and dried after washing with hexanes. MS m/z 253.1 (M+1).
Aufarbeitung
- temperatureThe reaction mixture is cooled to 0° C.
- customthe cyclized product is crystallized out
- filtrationThe compound is collected by filtration
- customdried
- washafter washing with hexanes
Quellen und Nachweise
- ORD-Eintrag
- ord-29beea0dbb9042dda025b86be76c15db
- Quelldatensatz
- uspto-grants-2013_10
- Patentnummer
- US08546370B2
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