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Acetic Anhydride → 3'-Azido-2',3'-dideoxy-5-bromouridine
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Acetic Anhydride | HCID 7918 | — |
| 反応物 | Bromine | HCID 24408 | — |
| 反応物 | Navuridine | HCID 55262 | — |
| 溶媒 | Acetic Acid | HCID 176 | — |
| 生成物 | 3'-Azido-2',3'-dideoxy-5-bromouridine | HCID 64978 | — |
反応手順
3'-Azido-5-bromo-2',3'-dideoxyuridine was prepared from the known 3'-azido-2',3'-dideoxyuridine (T. A. Krenitsky, et al., J. Med. Chem., 26, 891, (1983)) (0.827 g, 3.3 mMol) by first acetylating the 5'-hydroxyl group with acetic anhydride (15 mL) then by brominating the 5 position by the addition of acetic acid (0.5 mL) and bromine (0.566 g). The red-brown solution was stirred at room temperature for two hours. The reaction was taken to an oil in vacuo and triturated with ethyl ether. The oil was dissolved in methanol ammonia to remove the acetyl group. The desired product was isolated by chromatography on silica gel by elution with CHCl3 :MeOH (95:5 v/v). The yield was 32%; mp=148°-149° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05064946 |
| 出典データセット | uspto-grants-1991_11 |
| ORD ID | ord-37707a9b32a64b05be2a81c10c953f47 |
| 出典メモ | uspto-grants-1991_11 |