참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Uridine Diphosphate | HCID 6031 | — |
| 반응물 | Tributylamine | HCID 7622 | — |
| 반응물 | Ammonium Bicarbonate | HCID 14013 | — |
| 반응물 | Tributylammonium | HCID 3724478 | — |
| 반응물 | Disodium uridine 5'-diphosphate | HCID 11957711 | — |
| 반응물 | Diuridine tetraphosphate tetrasodium salt | HCID 131724809 | — |
| 생성물 | rUrd.rUrd.P-P-P-P | HCID 131723853 | — |
반응 단계
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.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07528119B2 |
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| 출처 데이터셋 | uspto-grants-2009_05 |
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| ORD ID | ord-7cf56a01c44540d3a55d570d2b60c997 |
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| 출처 메모 | uspto-grants-2009_05 |
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