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HRID 973792作成日:2026年10月25日

Acetic Anhydride → 3'-Azido-2',3'-dideoxy-5-bromouridine

https://huagongshe.com/reaction/973792

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic AnhydrideHCID 7918—
反応物BromineHCID 24408—
反応物NavuridineHCID 55262—
溶媒Acetic AcidHCID 176—
生成物3'-Azido-2',3'-dideoxy-5-bromouridineHCID 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

DOI10.6084/m9.figshare.5104873.v1
特許番号US05064946
出典データセットuspto-grants-1991_11
ORD IDord-37707a9b32a64b05be2a81c10c953f47
出典メモuspto-grants-1991_11