Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Methanol | HCID 887 | — |
| Edukt | Lithium Hydroxide | HCID 3939 | — |
| Edukt | Chloroform | HCID 6212 | — |
| Edukt | 2',3',5'-Tri-O-acetyl-2-fluoroadenosine | HCID 21816271 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | 1,4-Dioxane | HCID 31275 | — |
| Produkt | 2-Fluoroadenosine | HCID 8975 | — |
Reaktionsschritte
2-Fluoro-2',3',5'-tri-O-acetyladenosine (0.41 9, 1.0 mmol, lt. yellow solid) was dissolved in a mixture of 1,4-dioxane (5 mL) and water (1 mL). The solution was stirred at ambient temperature and solid LiOH.circle-solid.H2O (1.40 mL, 3.5 mmol) was added in one portion. The progress of the reaction was monitored by TLC (9:1 Chloroform:methanol). After 2 hours, most of the suspended solid had dissolved and TLC showed no acetylated intermediates remaining. The cloudy reaction mixture was poured directly onto a column of AG 50-X4 (H+, 100-200 mesh, 10 mL bed volume) ion exchange resin and the column was eluted with several column volumes of 1:1 methanol:water. 2-Fluoroadenosine began to elute immediately, and all fractions which contained 2-fluoroadenosine were concentrated under vacuum to obtain a white partially crystalline solid which was dried overnight at 60° C. under vacuum: 0.18 g (63% yield), mp 227°-230° C. (d). This material was consistent by TLC, IR and UV with an authentic sample of 2-fluoroadenosine.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05668270 |
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| Quelldatensatz | uspto-grants-1997_09 |
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| ORD ID | ord-01a8c0f8a55a4c0ea9634153471fead5 |
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| Quellennotiz | uspto-grants-1997_09 |
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