Reaktionsgleichung
[NH2:1][C:2]1[C:3](=[O:14])[N:4]([CH2:12][CH3:13])[C:5](=[O:11])[N:6]([CH2:9][CH3:10])[C:7]=1[NH2:8].[CH3:15][O:16][C:17]1[CH:27]=[CH:26][C:20]([CH:21]=[CH:22][C:23](O)=O)=[C:19]([CH3:28])[C:18]=1[CH3:29]>>[CH2:12]([N:4]1[C:3](=[O:14])[C:2]2[NH:1][C:23](/[CH:22]=[CH:21]/[C:20]3[CH:26]=[CH:27][C:17]([O:16][CH3:15])=[C:18]([CH3:29])[C:19]=3[CH3:28])=[N:8][C:7]=2[N:6]([CH2:9][CH3:10])[C:5]1=[O:11])[CH3:13]Komponenten
3
Versuchsvorschrift
Substantially the same procedure as in Example 7 was repeated using 2.5 g (12.6 mmol) of 5,6-diamino-1,3-diethyluracil and 2.9 g (13.9 mmol) of 4-methoxy-2,3-dimethylcinnamic acid. Then, the resultant crude crystals were recrystallized from ethanol/water to give 0.80 g (yield of Compound 72 as white crystals.
Aufarbeitung
- customThen, the resultant crude crystals were recrystallized from ethanol/water
Quellen und Nachweise
- ORD-Eintrag
- ord-87dc8dc2faf64499a136372f41208257
- Quelldatensatz
- uspto-grants-1996_01
- Patentnummer
- US05484920
Verknüpfte Notizen
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