Reaktionsgleichung
Cl[C:2]1[N:7]([CH3:8])[C:6](=[O:9])[N:5]([CH3:10])[C:4](=[O:11])[C:3]=1[CH:12]=[O:13].[CH2:14]([SH:16])[CH3:15]>>[CH2:14]([S:16][C:2]1[N:7]([CH3:8])[C:6](=[O:9])[N:5]([CH3:10])[C:4](=[O:11])[C:3]=1[CH:12]=[O:13])[CH3:15]Komponenten
3
Versuchsvorschrift
The process described in Method D was followed. 6-Chloro-1,3-dimethyl-2,4-dioxo-1,2,3,4-tetrahydropyrimidine-5-carbaldehyde (0.303 g, 1.50 mmol) and ethanethiol were used to obtain the title compound. The crude product was purified by column chromatography with a mixture of n-hexane:ethyl acetate (1:1) as the eluent.
Quellen und Nachweise
- ORD-Eintrag
- ord-dbafb17038e6410e997a1aa39eb95162
- Quelldatensatz
- uspto-grants-2013_09
- Patentnummer
- US08536210B2
Verknüpfte Notizen
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