Reaktionsgleichung
[C:1]([CH2:3][C:4]([NH2:6])=[S:5])#[N:2].[C:7]([C:11]1[CH:12]=[C:13]([CH:16]=[C:17]([C:19]([CH3:22])([CH3:21])[CH3:20])[CH:18]=1)[CH:14]=O)([CH3:10])([CH3:9])[CH3:8]>>[C:1]([C:3](=[CH:14][C:13]1[CH:12]=[C:11]([C:7]([CH3:9])([CH3:8])[CH3:10])[CH:18]=[C:17]([C:19]([CH3:22])([CH3:21])[CH3:20])[CH:16]=1)[C:4](=[S:5])[NH2:6])#[N:2]Komponenten
3
Versuchsvorschrift
Following the procedure as set forth in Example 11 above, cyanothioacetamide was condensed with 3,5-di-tert butylbenzaldehyde to yield the title compound, m.p. 172°-174° C.
Quellen und Nachweise
- ORD-Eintrag
- ord-ac3518b0caa1453cb745d78df7523da0
- Quelldatensatz
- uspto-grants-2005_07
- Patentnummer
- USRE038761E1
Verknüpfte Notizen
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