首页> 外国专利> RIBONUCLEOSIDE ANALOG HAVING AZIDE GROUPS AND METHOD FOR PRODUCING SAME, AND CHIMERA-TYPE OLIGORIBONUCLEOTIDE ANALOG CONTAINING TRIAZOLE LINKING-TYPE OLIGORIBONUCLEOTIDE FORMED FROM SUCH ANALOG

RIBONUCLEOSIDE ANALOG HAVING AZIDE GROUPS AND METHOD FOR PRODUCING SAME, AND CHIMERA-TYPE OLIGORIBONUCLEOTIDE ANALOG CONTAINING TRIAZOLE LINKING-TYPE OLIGORIBONUCLEOTIDE FORMED FROM SUCH ANALOG

机译:具有叠氮基团的核糖核苷类似物及其制备方法,以及由此类类似物形成的含三唑键合型寡聚核苷酸的化纤型寡核糖核苷酸类似物

摘要

Provided is a means for producing a non-natural nucleoside analog in which position 5 is a hydroxyl group and which is for synthesizing a triazole linking-type non-natural nucleotide having a structure bonded via organic groups containing 1,2,3-triazole rings. The present invention is related to a method for producing a compound represented by formula (Ic) (in the formula, each X is independently selected from a purine base and a pyrimidine base, and PG2 and PG5 are each independently hydrogen or a protector group) wherein, the method includes performing 3β-azidation of the 3α-hydroxyl of D-xylose using D-xylose as the starting material, and bonding the purine base or pyrimidine base at position 1.
机译:提供了一种制备非天然核苷类似物的方法,其中位置5是羟基,并且用于合成具有通过包含1,2,3-三唑环的有机基团键合的结构的三唑连接型非天然核苷酸。本发明涉及一种制备由式(Ic)表示的化合物的方法(在该式中,每个X独立地选自嘌呤碱和嘧啶碱,PG 2 和PG < Sup> 5 各自独立地是氢或保护基),其中,该方法包括使用D-木糖作为起始原料对D-木糖的3α-羟基进行3β-叠氮化,并结合嘌呤碱基或嘧啶在位置1。

著录项

  • 公开/公告号WO2015137121A1

    专利类型

  • 公开/公告日2015-09-17

    原文格式PDF

  • 申请/专利权人 TOHOKU UNIVERSITY;

    申请/专利号WO2015JP55405

  • 申请日2015-02-25

  • 分类号C07H19/067;C07H19/167;C07H21;C12N15/09;

  • 国家 WO

  • 入库时间 2022-08-21 15:04:17

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