참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Methanol | HCID 887 | — |
| 반응물 | Chloroform | HCID 6212 | — |
| 반응물 | Sodium Hydroxide | HCID 14798 | — |
| 반응물 | 2',3',5'-Tri-O-acetyl-2-fluoroadenosine | HCID 21816271 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | 1,4-Dioxane | HCID 31275 | — |
| 생성물 | 2-Fluoroadenosine | HCID 8975 | — |
반응 단계
2-Fluoro-2',3',5'-tri-O-acetyladenosine (0.41 g, 10 mmol) was dissolved in a mixture of 1,4-dioxane (7 mL) and water (2 mL) and the solution was cooled in an icewater bath. 2.5M NaOH (1.40 mL, 3.5 mmol) was added dropwise with vigorous stirring over a 2 min. period. The resulting bright yellow solution was stirred at 0° C. and monitored by TLC (9:1 Chloroform:methanol). After 2 hours, most of the yellow color had faded and TLC showed no acetylated intermediates remaining. The homogeneous 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: 0.20 g (70% yield), mp 220°-227° C. (d). This material was consistent by TLC, IR and UV with an authentic sample of 2-fluoroadenosine.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05668270 |
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| 출처 데이터셋 | uspto-grants-1997_09 |
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| ORD ID | ord-a98569d7c6024972885b818bf8e81d12 |
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| 출처 메모 | uspto-grants-1997_09 |
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