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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 465713생성일: 2026년 10월 24일

Citrate → [(2S,3S,5R)-5-(2-amino-6-ethoxy-purin-9-yl)-3-azido-tetrahydrofuran-2-yl]methanol

https://huagongshe.com/ko/reaction/465713

반응식

참여 물질

역할이름HCID투입량
반응물CitrateHCID 31348—
반응물ZidovudineHCID 35370—
반응물6-ethoxy-9H-purin-2-amineHCID 95805—
생성물[(2S,3S,5R)-5-(2-amino-6-ethoxy-purin-9-yl)-3-azido-tetrahydrofuran-2-yl]methanolHCID 476439—

반응 조건

온도50 °C

반응 단계

To 500 mL of an aqueous pH 6.0, 50 mM citrate buffer, prepared as described in Example 2c, was added 2-amino-6-ethoxypurine (0.0895 g, 0.5 mmol) and 3'-azido-3'-deoxythymidine (0.668 g, 2.5 mmol). Solution was achieved by heating the mixture at 50° C. with sonication. A sample was removed as a control. A 24 mL solution of trans-N-deoxyribosylase (Example 2b) at an activity of 1400 units/mL was added. The reaction was heated at 50° C. Four days later 0.089 g, 0.5 mmol, of 2-amino-6-ethoxypurine was added to the reaction. The reaction was terminated after eleven days. The reaction was heated to 80° C. to precipitate the enzyme and then filtered. The aqueous solution was extracted with ethyl acetate to remove the product. The combined ethyl acetate fractions were dried with magnesium sulfate, filtered and the solvent removed in vacuo to give a foam. The foam was chromatographed on 180 g of silica gel (230-400 mesh) eluted with chloroform/methanol (98:2. v/v). The product containing fractions were combined and the solvent removed in vacuo to give the product as an oil. The oil was dissolved in water and lyophilized to give a solid (55% yield).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05153318
출처 데이터셋uspto-grants-1992_10
ORD IDord-2632dee7f226419094fe236e2a857f4f
출처 메모uspto-grants-1992_10