Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | p-Toluenesulfonic acid | HCID 6101 | — |
| Edukt | Acetic Anhydride | HCID 7918 | — |
| Edukt | 1,3-Dioxolane | HCID 12586 | — |
| Edukt | Diacetylguanine | HCID 136360183 | — |
| Lösungsmittel | Toluene | HCID 1140 | — |
| Produkt | Acyclovir | HCID 135398513 | 21,6% |
Reaktionsschritte
To a mixture of acetic anhydride (1.2 ml) and p-toluenesulfonic acid (0.09 g) was added with stirring dioxolane (1.02 g) - caution, exothermic. The solution was allowed to cool for several minutes. Diacetylguanine (1.45 g) and dry toluene (9 ml) were added and the reaction mixture was stirred at reflux for 18 hr. and then allowed to cool to room temperature. The toluene was decanted off and the residue triturated several times with benzene. Methanol (10 ml) was added to the residue and evaporated under reduced pressure. To the residue was added 40% aqueous methylamine (10 ml) and the mixture heated on a steam bath for 20 min. The water and methylamine were removed under reduced pressure, ethanol (10 ml) was added and evaporated. The residue was thoroughly extracted with boiling methanol (700 ml total) and the combined extracts evaporated. The resulting solid was triturated with cold ethanol and then recrystallized from methanol to give 9-(2-hydroxyethoxymethyl)guanine (0.3 g).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04146715 |
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| Quelldatensatz | uspto-grants-1979_03 |
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| ORD ID | ord-bac7624945f849798d84013f303db8d7 |
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| Quellennotiz | uspto-grants-1979_03 |
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