4-Methylphenyl isocyanate → 3-ethoxycarbonyl-9-(4-methylphenylcarbamoylthio)-4H-pyrido[1,2-a]pyrimidin-4-one
Reaktionsgleichung
[CH2:1]([O:3][C:4]([C:6]1[C:11](=[O:12])[N:10]2[CH:13]=[CH:14][CH:15]=[C:16]([SH:17])[C:9]2=[N:8][CH:7]=1)=[O:5])[CH3:2].[CH3:18][C:19]1[CH:24]=[CH:23][C:22]([N:25]=[C:26]=[O:27])=[CH:21][CH:20]=1>C(Cl)Cl>[CH2:1]([O:3][C:4]([C:6]1[C:11](=[O:12])[N:10]2[CH:13]=[CH:14][CH:15]=[C:16]([S:17][C:26](=[O:27])[NH:25][C:22]3[CH:23]=[CH:24][C:19]([CH3:18])=[CH:20][CH:21]=3)[C:9]2=[N:8][CH:7]=1)=[O:5])[CH3:2]Komponenten
4
Versuchsvorschrift
To a suspension of 0.4 g of 3-ethoxycarbonyl-9-mercapto-4H-pyrido[1,2-a]pyrimidin-4-one II-1 in 10 ml of dry CH2Cl2 is added 0.35 g of 4-methylphenyl isocyanate III-1, and the resultant mixture is stirred at room temperature for 4 hours. At this time the reaction mixture is crystallized again after it is once dissolved.
Aufarbeitung
- customAt this time the reaction mixture is crystallized again after it
- dissolutionis once dissolved
Quellen und Nachweise
- ORD-Eintrag
- ord-4de4c8e5f401416d8f77e6bee5ed4658
- Quelldatensatz
- uspto-grants-1989_06
- Patentnummer
- US04840953
Notizen zur Reaktion
Wird geladen…