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HRID 1075559作成日:2026年10月27日

O-Benzoyllamivudine → Lamivudine

https://huagongshe.com/reaction/1075559

反応式

関与物質

役割名称HCID仕込み量
反応物O-BenzoyllamivudineHCID 10903732—
溶媒MethanolHCID 887—
生成物LamivudineHCID 6082590.4%

反応手順

A suspension of (cis)-4-amino-1-(2-benzoyloxymethyl-1,3-oxathiolan-5-yl)(1H)-pyrimidin-2-one (Intermediate 3) (8.19 g) and Amberlite IRA-400 (OH) resin (8.24 g) in methanol (250 ml) was stirred and heated to reflux for 11/4 h. Solids were removed by filtration then washed with methanol. The combined filtrates were evaporated. The residue was triturated with ethyl acetate (80 ml). The resulting white solid was collected by filtration to give the title product (5.09 g), 1H NMR (DMSO-d6) 3.04 (1H), 3.40 (1H), 3.73 (2H), 5.18 (1H), 5.29 (1H), 5.73 (1H), 6.21 (1H), 7.19 (2H), 7,81 (1H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05905082
出典データセットuspto-grants-1999_05
ORD IDord-c9cce1c6c73d40baa1fedc1e1bd85be0
出典メモuspto-grants-1999_05