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Synthesis of quinazolinimines and quinazolinamines from 2-fluorobenzonitriles under catalyst-free conditions

机译:在无催化剂条件下由2-氟苄腈合成喹唑啉亚胺和喹唑啉胺

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摘要

A convenient procedure for the synthesis of quinazolinimines and quinazolinamines from 2-fluorobenzonitriles has been developed. By using KO~tBu as the promotor with 2-aminopyridines or amidines as the reaction partner, the desired heterocycles were produced in moderate to good yields under catalyst-free conditions.
机译:已经开发了从2-氟苄腈合成喹唑啉亚胺和喹唑啉胺的简便方法。通过使用KO-tBu作为促进剂,以2-氨基吡啶或as作为反应伙伴,在无催化剂条件下以中等至良好的产率产生了所需的杂环。

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  • 来源
    《Organic & biomolecular chemistry》 |2015年第43期|10656-10662|共7页
  • 作者

    Jian-Bo Feng; Xiao-Feng Wu;

  • 作者单位

    Department of Chemistry, Zhejiang Sci-Tech University, Xiasha Campus, Hangzhou, Zhejiang Province 310018, People's Republic of China,Leibniz-Institut fuer Katalyse e.V. an der Universitaet Rostock, Albert-Einstein-Strasse 29a, 18059 Rostock, Germany;

    Department of Chemistry, Zhejiang Sci-Tech University, Xiasha Campus, Hangzhou, Zhejiang Province 310018, People's Republic of China,Leibniz-Institut fuer Katalyse e.V. an der Universitaet Rostock, Albert-Einstein-Strasse 29a, 18059 Rostock, Germany;

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