Reaktionsgleichung
[CH2:1]([N:4]=[C:5]([NH2:21])[NH:6][C:7]1[CH:12]=[CH:11][N:10]=[C:9]([CH2:13][CH2:14][CH2:15][CH2:16][C:17](=[NH:20])OC)[N:8]=1)[CH2:2][CH3:3].[Cl-:22].[NH4+:23]>CO>[ClH:22].[CH2:1]([N:4]=[C:5]([NH2:21])[NH:6][C:7]1[CH:12]=[CH:11][N:10]=[C:9]([CH2:13][CH2:14][CH2:15][CH2:16][C:17]([NH2:23])=[NH:20])[N:8]=1)[CH2:2][CH3:3]Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
A mixture of methyl 5-(4-[2-propylguanidino]pyrimid-2-yl)valerimidate (0.4 g.) and ammonium chloride (0.076 g.) in MeOH (20 ml.) was stirred at ambient temperature for 1 hour and the solvent evaporated in vacuo to give 5-(4-[2-propylguanidino]pyrimid-2-yl)valeramidine hydrochloride (0.4 g.) as an oil which was used without further purification.
Aufarbeitung
- customthe solvent evaporated in vacuo
Quellen und Nachweise
- ORD-Eintrag
- ord-9f68561694d34a0d9c0e9e77265079fc
- Quelldatensatz
- uspto-grants-1988_05
- Patentnummer
- US04748165
Verknüpfte Notizen
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