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首页> 外文期刊>Molecules >Synthesis of 1-(2'-Deoxy-?-D-ribofuranosyl)-1H-imidazo[4,5-d]-pyridazine-4,7(5H,6H)-dione: A Potential Building Block for Antisense Applications
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Synthesis of 1-(2'-Deoxy-?-D-ribofuranosyl)-1H-imidazo[4,5-d]-pyridazine-4,7(5H,6H)-dione: A Potential Building Block for Antisense Applications

机译:1-(2'-脱氧-α-D-呋喃呋喃糖基)-1H-咪唑并[4,5-d]-哒嗪-4,7(5H,6H)-二酮的合成:反义应用的潜在基础

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摘要

Synthesis of the title compound,1-(2'-deoxy-b-D-ribofuranosyl)-1H-imidazo[4,5-d]pyridazine-4,7(5H,6H)-dione (1), is reported. It was synthesized in five steps, commencing with methyl 1-(b-D-ribofuranosyl)imidazo-4,5-dicarboxylate (2). The 3',5'-hydroxyl groups of 2 were protected with a bis-silylating agent to form 3, which was then converted into the corresponding 2'-thionocarbonate derivative 5. The reduction of the latter with tri-n-butyltin hydride (to form 6), followed by silyl deprotection with tetra-nbutylammonium fluoride, afforded 7. Treatment of the latter with hydrazine hydrate yielded the target nucleoside 1.
机译:据报道,标题化合物1-(2′-脱氧-b-D-核呋喃糖基)-1H-咪唑并[4,5-d]哒嗪-4,7(5H,6H)-二酮(1)的合成。从1-(b-D-核呋喃糖基)咪唑-4,5-二羧酸甲酯(2)开始,分五步合成。用双甲硅烷基化剂保护2的3',5'-羟基以形成3,然后将其转化为相应的2'-硫代碳酸酯衍生物5。用氢化三正丁基锡将后者还原(生成6),然后用四正丁基氟化铵进行甲硅烷基脱保护,得到7。用水合肼处理后者,得到目标核苷1。

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