Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Uridine Diphosphate | HCID 6031 | — |
| Reactant | Tributylamine | HCID 7622 | — |
| Reactant | Ammonium Bicarbonate | HCID 14013 | — |
| Reactant | Tributylammonium | HCID 3724478 | — |
| Reactant | Disodium uridine 5'-diphosphate | HCID 11957711 | — |
| Reactant | Diuridine tetraphosphate tetrasodium salt | HCID 131724809 | — |
| Product | rUrd.rUrd.P-P-P-P | HCID 131723853 | — |
Reaction Steps
The present invention provides the synthesis of diuridine tetraphosphate tetrasodium salt via the tetraammonium salt. In this process, uridine 5′-diphosphate disodium salt is first converted to the tributylammonium salt using a sulfonic acid resin to generate UDP as the free acid, followed by salt formation with excess tributylamine. After isolation by evaporative water removal, the anhydrous UDP tributylammonium salt is activated with 1,1-carbonyldiimidazole in DMF solution, during which time coupling to form U2P4 also occurs. Concentration of the solution in vacuo, followed by ion-exchange chromatography on Sephadex DEAE-A25 using an increasing gradient of aqueous ammonium bicarbonate yielded a solution of pure diuridine tetraphosphate in ammonium bicarbonate buffer. The volatile buffer is removed by repeated evaporation with water on a rotary evaporator to generate the tetraammonium salt of U2P4 as oil. The oil is dissolved in deionized water to give a ca. 10% solution, and this solution is charged to a Dowex 50W×4 Na+ (Dow) column and eluted with deionized water. The fractions containing U2P4 are pooled, concentrated and lyophilized to yield U2P4 tetrasodium salt as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06872710B2 |
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| Source dataset | uspto-grants-2005_03 |
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| ORD ID | ord-7c3ae6450c7a42018e55542fd2ea202a |
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| Source note | uspto-grants-2005_03 |
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