Water → HCID 178507908, Verbindung
Reaktionsgleichung
[NH:1]1[CH:8]=[CH:7][C:5]([NH2:6])=[N:4][C:2]1=[S:3].[OH-].[Na+].Cl[CH2:12][CH2:13][CH2:14][C:15]1[N:16]=[CH:17][NH:18][CH:19]=1.O>CCO>[NH2:6][C:5]1[CH:7]=[CH:8][N:1]=[C:2]([S:3][CH2:12][CH2:13][CH2:14][C:15]2[N:16]=[CH:17][NH:18][CH:19]=2)[N:4]=1Komponenten
6
Edukt 4
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
A mixture of thiocytosine (0.7 g.), sodium hydroxide(0.22 g.) and 4-(3-chloropropyl)imidazole (0.8 g.) was stirred in EtOH (8 ml.) and water (8 ml.) at room temperature for 16 hours and then heated under reflux for 2 hours. The solution was evaporated to dryness and the residue partitioned between dilute aqueous sodium hydroxide (20 ml.) and EtOAc (30 ml.). The EtOAc layer was evaporated to dryness to give 4-[3-(4-aminopyrimid-2-ylthio)propyl]imidazole as a brown gum which was used without further purification.
Aufarbeitung
- temperatureheated
- temperatureunder reflux for 2 hours
- customThe solution was evaporated to dryness
- customthe residue partitioned between dilute aqueous sodium hydroxide (20 ml.) and EtOAc (30 ml.)
- customThe EtOAc layer was evaporated to dryness
Quellen und Nachweise
- ORD-Eintrag
- ord-f2b320253dad4fc79b9a71707662fa09
- Quelldatensatz
- uspto-grants-1984_07
- Patentnummer
- US04463005
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