Simple Strategy for Benzo[<i>de</i>]chromene‐7,8‐dione Synthesis via Tandem Sonogashira Coupling and Intramolecular Cyclization Reactions

DOI Web Site Web Site 参考文献54件
  • Masashi Yokoya
    Department of Pharmaceutical Chemistry Meiji Pharmaceutical University 2-522-1, Noshio Kiyose Tokyo 204-8588 Japan
  • Takaaki Ishiguro
    Department of Pharmaceutical Chemistry Meiji Pharmaceutical University 2-522-1, Noshio Kiyose Tokyo 204-8588 Japan
  • Yoshiaki Sakairi
    Department of Infection Control Science Meiji Pharmaceutical University 2-522-1, Noshio Kiyose Tokyo 204-8588 Japan
  • Shinya Kimura
    Department of Pharmaceutical Chemistry Meiji Pharmaceutical University 2-522-1, Noshio Kiyose Tokyo 204-8588 Japan
  • Yuji Morita
    Department of Infection Control Science Meiji Pharmaceutical University 2-522-1, Noshio Kiyose Tokyo 204-8588 Japan
  • Masamichi Yamanaka
    Department of Pharmaceutical Chemistry Meiji Pharmaceutical University 2-522-1, Noshio Kiyose Tokyo 204-8588 Japan

抄録

<jats:title>Abstract</jats:title><jats:p>Benzo[<jats:italic>de</jats:italic>]chromene‐7,8‐dione derivatives are known to have important biological and pharmacological properties. Thus, a novel and efficient method was developed for the synthesis of benzo[<jats:italic>de</jats:italic>]chromene‐7,8‐dione derivatives via the tandem reaction of 5‐bromo‐2‐hydroxynaphthalene‐1,4‐dione and terminal alkynes, which proceeds under the typical reaction conditions for Sonogashira coupling using Pd and Cu catalysts. The process likely occurs via a tandem reaction due to the synthesized Sonogashira coupling product undergoing intramolecular cyclization in the presence of a Cu catalyst. This method is superior to existing synthesis methods in that it can access benzo[<jats:italic>de</jats:italic>]chromene‐7,8‐dione compounds without the post‐oxidation of benzo[<jats:italic>de</jats:italic>]chromenes. Furthermore, it enables the direct supply of several biologically active compounds. The minimum inhibitory concentrations (MICs) of the synthesized compounds against multidrug efflux pump‐deficient strains of <jats:italic>S. aureus</jats:italic>, <jats:italic>E. coli</jats:italic>, and <jats:italic>P. aeruginosa</jats:italic> and their parent strains were determined. Certain synthesized compounds exhibited strong antimicrobial activity, indicating that they are substrates for multidrug efflux pumps.</jats:p>

収録刊行物

参考文献 (54)*注記

もっと見る

関連プロジェクト

もっと見る

キーワード

詳細情報 詳細情報について

問題の指摘

ページトップへ