関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Floxuridine | HCID 5790 | — |
| 反応物 | Triethylamine | HCID 8471 | — |
| 反応物 | Tetrahydro-2-furyl acetate | HCID 102657 | — |
| 反応物 | N,O-bis(trimethylsilyl)acetamide | HCID 6913588 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | 2'-Deoxy-5-fluoro-3-(2-tetrahydrofuranyl)uridine | HCID 13715002 | 81.7% |
反応手順
A 16.5 g quantity of N,O-bis(trimethylsilyl) acetamide was added to a suspension of 5.00 g of 2'-deoxy-5-fluorouridine in 50 ml of dry dichloromethane at room temperature with stirring, and the mixture was stirred for four hours. Then a solution of 4.00 g of 2-acetoxytetrahydrofuran and 1.17 ml of stannic chloride in 10 ml of dry dichloromethane was added and the mixture was stirred for 1.5 hours. Then 8.0 ml of triethylamine was added to neutralize the mixture and the mixture was washed with water. The dichloromethane layer was concentrated and the residue was dissolved in 100 ml of methanol. A 3 ml quantity of acetic acid was added thereto and the mixture was left to stand at 40° C. for 3 hours. The solvent was distilled off and the residue was applied to a silica gel column to conduct gradient elution using chloroform and methanol (up to 4%)-chloroform mixtures, giving 5.25 g of 2'-deoxy-5-fluoro-3-(2-tetrahydrofuranyl)uridine as an oil in a yield of 81.7%.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04864021 |
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| 出典データセット | uspto-grants-1989_09 |
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| ORD ID | ord-e997426edcb4409b9375fae517d71f4f |
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| 出典メモ | uspto-grants-1989_09 |
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