CAS: 443642-30-6; α-D-Erythro-Pentofuranosid-2-Ulose, Methyl 3,5-Bis-O-[(2,4-Dichlorophenyl)Methyl]-

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    上下游产品

    (3R,4S,5R)-4-((2,4-dichlorobenzyl)oxy)-5-(((2,4-dichlorobenzyl)oxy)methyl)-2-methoxytetrahydrofuran-3-ol (2R,3R,4R)-3,4-bis((2,4-dichlorobenzyl)oxy)-2-(((2,4-dichlorobenzyl)oxy)methyl)-5-methoxytetrahydrofuran 2-O-acetyl-3,5-bis-O-(2,4-dichlorophenylmethyl)-1-O-methyl-α-D-ribofuranose 3,5-bis-O-(2,4-dichlorophenylmethyl)-2-C-ethyl-1-O-methyl-α-D-ribofuranose (2S,3R,4R,5R)-4-((2,4-dichlorobenzyl)oxy)-5-(((2,4-dichlorobenzyl)oxy)methyl)-2-methoxy-3-methyltetrahydrofuran-3-ol 7-deaza-2'-C-methyl-adenosine 4-chloro-5-methyl-7-(2-C-methyl-β-D-ribofuranosyl)-7H-pyrrolo[2,3-d]pyrimidine

    合成工艺路线路线简述

    • 合成目标产物 1-O-Methyl-3,5-Bis-O-[(2,4-Dichlorophenyl)Methyl]-Alpha-D-Erthro-Pentofuranoside-2-Ulose 主要起始原料 1-Methyl-3,5-Bis-O-(2,4-Dichlorobenzyl)-Alpha-D-Ribofuranoside
    • (文献来源)合成步骤主要原料 1-Methyl-3,5-Bis-O-(2,4-Dichlorobenzyl)-Alpha-D-Ribofuranoside
    📜Methyl 2,3,5-Tri-O-(2,4-Dichlorobenzyl)-D-Ribofuranoside置于三氯异氰尿酸,四氯化锡体系中,用 二氯甲烷 作为反应溶剂,化学反应 6.17H,反应生成 1-O-甲基-3,5-二-O-[(2,4-二氯苯基)甲基]-Alpha-D-赤式戊呋喃糖苷-2-酮
    参考文献:Discovery Of 2'-α-C-Methyl-2'-β-C-Fluorouridine Phosphoramidate Prodrugs As Inhibitors Of Hepatitis C Virus
    标题:Discovery Of 2'-α-C-Methyl-2'-β-C-Fluorouridine Phosphoramidate Prodrugs As Inhibitors Of Hepatitis C Virus
    摘要:2'-Alpha-C-Methyl-2'-Beta-C-Fluorouridine And Its Phosphoramidate Prodrugs Were Synthesized And Evaluated For Their Inhibitory Activity Against Hcv. The Structure-Activity Relationship Analysis Of The Phosphoramidate Moiety Found That 17M,17Q,And 17R Exhibit Potent Activities Against Hcv,With Ec50 Values Of 1.82 +/-0.19,0.88 +/-0.12,And 2.24 +/-0.22 Mu M,Respectively. The Docking Study Revealed That The Recognition Of The 2'-Beta-F By Arg158,3'-Oh By N291,And The Watson Crick Pairing With The Template Allowed 23 To Form The In-Line Conformation Necessary For Its Incorporation Into The Viral Rna Chain.
    DOI:10.1021/acsmedchemlett.6B00270

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    ✅ COA系统入驻 | 共享模式

    合成参考文献

    参考DOI号:10.1021/acsmedchemlett.6b00270
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