Reaktionsgleichung
[Na].Cl[C:3]1[N:8]=[C:7]([NH:9][CH:10]2[CH2:12][CH2:11]2)[N:6]=[C:5]([NH:13][CH:14]([CH3:16])[CH3:15])[N:4]=1.[CH3:17][OH:18]>>[CH3:17][O:18][C:3]1[N:8]=[C:7]([NH:9][CH:10]2[CH2:12][CH2:11]2)[N:6]=[C:5]([NH:13][CH:14]([CH3:16])[CH3:15])[N:4]=1Komponenten
4
Versuchsvorschrift
2.1 g of sodium was added in portions to 400 ml of stirred anhydrous methanol. The solution was allowed to cool to room temperature, then 16.5 g of 9B was added and the mixture was refluxed for 2 hours. The solvent was evaporated, and the residue was washed with water, then extracted with ether. The extract phase was dried (MgSO4) and stripped of solvent to give 2-methoxy-4-(cyclopropylamino)-6-(1-methylethylamino)-1,3,5-triazine (13A).
Aufarbeitung
- temperaturethe mixture was refluxed for 2 hours
- customThe solvent was evaporated
- washthe residue was washed with water
- extractionextracted with ether
- dry with materialThe extract phase was dried (MgSO4)
Quellen und Nachweise
- ORD-Eintrag
- ord-a3dd8f3efd3d43f2ba7a1f82d6b37e86
- Quelldatensatz
- uspto-grants-1985_07
- Patentnummer
- US04528027
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