首页> 外国专利> PREPARATION OF 9-(BETA-D-ARABINOFURANOSYL)ADENINE

PREPARATION OF 9-(BETA-D-ARABINOFURANOSYL)ADENINE

机译:9-(BETA-D-阿拉伯呋喃糖基)腺嘌呤的制备

摘要

PURPOSE:To obtain the titled compound useful as an antiviral agent, etc. industrially advantageously, treating a specific siloxane-containing adenosine with dimethyl sulfoxide and acetic anhydride, reducing the reaction product, circulating a starting substance prepared as a by-product, eliminating a protecting group from the reduction product. CONSTITUTION:A 3',5'-O-(tetraisopropyldisiloxane-1,3-diyl)adenosine shown by the formula I (R is isopropyl group) is treated with dimethyl sulfoxide and acetic anhydride to give a corresponding 2'-keto derivative shown by the formula II. This substance is reduced, 9-[3',5'-O-(tetraisopropyldisiloxane-1,3-diyl)-beta-D-arabinofuranosyl ]adenosine shown by the formula III and the starting substance are separated from the reaction mixture, the latter is circulated through the first process, the protecting group is eliminated from the reduction product shown by the formula III, to give the desired compound shown by the formula IV.
机译:用途:为了获得在工业上有利地用作抗病毒剂等的标题化合物,用二甲基亚砜和乙酸酐处理特定的含硅氧烷的腺苷,还原反应产物,循环制备为副产物的起始物质,消除还原产物的保护基。组成:将式I所示的3',5'-O-(四异丙基二硅氧烷-1,3-二基)腺苷(R为异丙基)用二甲基亚砜和乙酸酐处理,得到所示的相应的2'-酮衍生物由公式二。将该物质还原,将式III所示的9- [3',5'-O-(四异丙基二硅氧烷-1,3-二基)-β-D-阿拉伯呋喃糖基]腺苷与原料从反应混合物中分离出来,后者通过第一过程循环,从式Ⅲ所示的还原产物中除去保护基,得到式Ⅳ所示的所需化合物。

著录项

  • 公开/公告号JPS635040B2

    专利类型

  • 公开/公告日1988-02-01

    原文格式PDF

  • 申请/专利权人 TOSHIN KEMIKARU KK;

    申请/专利号JP19820123913

  • 申请日1982-07-16

  • 分类号C07H19/19;C07H19/16;

  • 国家 JP

  • 入库时间 2022-08-22 07:02:49

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