Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Uracil | HCID 1174 | — |
| Reactant | Pyrimidine, 2,4-bis[(trimethylsilyl)oxy]- | HCID 82640 | — |
| Reactant | Ammonium Sulfate | HCID 6097028 | — |
| Reactant | HCID 9975824 | HCID 9975824 | — |
| Solvent | Hexamethyldisilazane | HCID 13838 | — |
| Product | HCID 70466634 | HCID 70466634 | — |
Reaction Steps
A mixture of 3-O-acetyl-5-O-benzoyl-2-deoxy-2-fluoro-D-arabinofuranosyl bromide (11.5 g) and 2,4-bis(trimethylsilyloxy)pyrimidine [prepared by refluxing a mixture of 5 g of uracil and 5-15 mg of ammonium sulfate in 25 ml of hexa-methyldisilazane until a clear solution is obtained followed by removal of the excess hexamethyldisilazane in vacuo] in 150 ml of methylene chloride is stirred for 5 days at room temperature. Methanol (5 ml) is added to the mixture and the suspension is filtered through a celite pad. The filtrate is evaporated in vacuo and the residue is triturated with diethyl ether to give a crude product which was recrystallized from ethanol to give pure 1-(3-O-acetyl-5-O-benzoyl-2-deoxy-2-fluoro-β-D-arabinofuranosyl)uracil, 5.8 g, m.p. 179°-180°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04211773 |
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| Source dataset | uspto-grants-1980_07 |
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| ORD ID | ord-94e6946fdca44ea7b42e89710461290b |
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| Source note | uspto-grants-1980_07 |
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