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A New Synthesis of 4, 4-Diaryl/Diheteroaryl-3-butenyl Derivatives of Nipecotic Acids as GABA Transporter Inhibitors

机译:萘甲酸作为GABA转运蛋白抑制剂的4,4-二芳基/二杂芳基-3-丁烯基衍生物的新合成

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摘要

A new method for the synthesis of 4, 4-diaryl/diheteroaryl-3-butenyl derivatives of nipecotic acid as GABA transporter inhibitors is described. The key intermediates 4-tosyl-1,1-diaryl/diheteroaryl-1-butene 10a-d were synthesized by Wittig reaction, and followed by alkylation with (R)-3-piperidinecarboxylate. The resulting N-cycloalkylated amino acid esters 11a-d were saponified and then acidified to get the target compounds 1a-d. The preliminary bioassays showed that 1a-d exhibited excellent inhibition of [3H]-GABA uptake in vitro of culture cells.
机译:描述了一种新的合成方法,该方法合成了作为GABA转运蛋白抑制剂的4种4-辛基/二杂芳基-三杂芳基-3-丁烯基衍生物。通过Wittig反应合成关键中间体4-甲苯磺酰基-1,1-二芳基/二杂芳基-1-丁烯10a-d,然后用(R)-3-哌啶羧酸酯烷基化。将所得的N-环烷基化的氨基酸酯11a-d皂化,然后酸化,得到目标化合物1a-d。初步的生物分析表明,1a-d对培养细胞在体外对[3H] -GABA的吸收表现出优异的抑制作用。

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  • 来源
    《中国化学快报(英文版)》 |2005年第9期|1205-1208|共4页
  • 作者

  • 作者单位

    Department of Medicinal Chemistry, School of Pharmacy, Fudan University, Shanghai 200032;

    Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, Shanghai 200032;

    Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, Shanghai 200032;

    Department of Medicinal Chemistry, School of Pharmacy, Fudan University, Shanghai 200032;

  • 收录信息 中国科技论文与引文数据库(CSTPCD);
  • 原文格式 PDF
  • 正文语种 chi
  • 中图分类 化学;
  • 关键词

    Tiagabine; nipecotic acid; derivatives; synthesis; GABA transporter inhibitor;

    机译:替加宾碱;喘息酸;衍生物;合成;GABA转运蛋白抑制剂;
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