Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trimethyl Phosphate | HCID 10541 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | HCID 474527 | HCID 474527 | — |
| Product | HCID 474929 | HCID 474929 | — |
Reaction Steps
2.7 g (6 mmol) N4 -palmitoyl-2',3'-dideoxycytidine is added gradually to a mixture of 1.09 ml (12 mmol) phosphorylchloride and 20 ml trimethylphosphate that is stirred at 0° C. The batch is stirred for a further 2 hours when cold and then slowly neutralized with 0.5N NaOH during cooling. The precipitate that is formed is centrifuged off, absorbed in chloroform/methanol; 7/3; V/V, filtered over sodium sulphate and freed of solvent in a vacuum. The residue so obtained is crystallized several times from ethanol. When this is done, 2.5 g of N4 -palmitoyl-2',3'-dideoxycytidine-5'-phosphate is obtained and this displays an Rf value of 0.35 on the silica gel plate in the chloroform/methanol; 1/1; V/V system.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05679652 |
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| Source dataset | uspto-grants-1997_10 |
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| ORD ID | ord-4d75de7a27e543479bb64fa7f0747bf2 |
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| Source note | uspto-grants-1997_10 |
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