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<article article-type="research-article" dtd-version="1.3" xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xml:lang="en"><front><journal-meta><journal-id journal-id-type="publisher-id">chemicallytech</journal-id><journal-title-group><journal-title xml:lang="en">Fine Chemical Technologies</journal-title><trans-title-group xml:lang="ru"><trans-title>Тонкие химические технологии</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">2410-6593</issn><issn pub-type="epub">2686-7575</issn><publisher><publisher-name>MIREA – Russian Technological University (RTU MIREA).</publisher-name></publisher></journal-meta><article-meta><article-id custom-type="elpub" pub-id-type="custom">chemicallytech-1444</article-id><article-categories><subj-group subj-group-type="heading"><subject>Research Article</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>CHEMISTRY AND TECHNOLOGY OF MEDICINAL COMPOUNDS AND BIOLOGICALLY ACTIVE SUBSTANCES</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="ru"><subject>ХИМИЯ И ТЕХНОЛОГИЯ ЛЕКАРСТВЕННЫХ ПРЕПАРАТОВ И БИОЛОГИЧЕСКИ АКТИВНЫХ СОЕДИНЕНИЙ</subject></subj-group></article-categories><title-group><article-title>Synthesis of substituted 2-(1,2,4- triazol-3-yl)benzimidazoles</article-title><trans-title-group xml:lang="ru"><trans-title>Cинтез 2-(1,2,4- триазол-3-ил)бензимидазольной библиотеки</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Иванова</surname><given-names>Н. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Ivanova</surname><given-names>N. V.</given-names></name></name-alternatives><email xlink:type="simple">noemail@neicon.ru</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Свиридов</surname><given-names>С. И.</given-names></name><name name-style="western" xml:lang="en"><surname>Sviridov</surname><given-names>S. I.</given-names></name></name-alternatives><email xlink:type="simple">noemail@neicon.ru</email><xref ref-type="aff" rid="aff-2"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Степанов</surname><given-names>А. Е.</given-names></name><name name-style="western" xml:lang="en"><surname>Stepanov</surname><given-names>A. E.</given-names></name></name-alternatives><email xlink:type="simple">noemail@neicon.ru</email><xref ref-type="aff" rid="aff-1"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>МИТХТ им. М.В. Ломоносова, 119571, Москва, пр-т Вернадского, д. 86</institution><country>Россия</country></aff><aff xml:lang="en"><institution>M.V. Lomonosov Moscow State University of Fine Chemical Technologies, 86, Vernadskogo pr., Moscow 119571</institution><country>Russian Federation</country></aff></aff-alternatives><aff xml:lang="ru" id="aff-2"><institution>ООО «Кембридж»</institution><country>Russian Federation</country></aff><pub-date pub-type="collection"><year>2006</year></pub-date><pub-date pub-type="epub"><day>28</day><month>10</month><year>2006</year></pub-date><volume>1</volume><issue>5</issue><fpage>79</fpage><lpage>82</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Ivanova N.V., Sviridov S.I., Stepanov A.E., 2006</copyright-statement><copyright-year>2006</copyright-year><copyright-holder xml:lang="ru">Иванова Н.В., Свиридов С.И., Степанов А.Е.</copyright-holder><copyright-holder xml:lang="en">Ivanova N.V., Sviridov S.I., Stepanov A.E.</copyright-holder><license xml:lang="ru" license-type="creative-commons-attribution" xlink:href="https://creativecommons.org/licenses/by/4.0/" xlink:type="simple"><license-p>Данная работа распространяется под лицензией Creative Commons Attribution 4.0.</license-p></license><license xml:lang="en" license-type="creative-commons-attribution" xlink:href="https://creativecommons.org/licenses/by/4.0/" xlink:type="simple"><license-p>This work is licensed under a Creative Commons Attribution 4.0 License.</license-p></license></permissions><self-uri xlink:href="https://www.finechem-mirea.ru/jour/article/view/1444">https://www.finechem-mirea.ru/jour/article/view/1444</self-uri><abstract><p>A solution-phase synthesis for the preparation of substituted 2-(1,2,4-triazol-3- yl)benzimidazoles from triazole aldehydes and ortho-phenylenediamines has been developed for the purpose of producing diverse lead generation libraries.</p></abstract><trans-abstract xml:lang="ru"><p>С использованием методов комби- наторной химии осуществлён син- тез 2-(1,2,4-триазол-3- ил)бензимидазольной библиотеки из триазолилальдегидов и фенилендиами- нов и проведено биохимическое тести- рование библиотеки на ингибирование киназной активности.</p></trans-abstract></article-meta></front><back><ref-list><title>References</title><ref id="cit1"><label>1</label><citation-alternatives><mixed-citation xml:lang="ru">Naito Y., Akahoshi F., Takeda S. //J. med. chem. – 1996. – V.39. – P. 3019-3029.</mixed-citation><mixed-citation xml:lang="en">Naito Y., Akahoshi F., Takeda S. //J. med. chem. – 1996. – V.39. – P. 3019-3029.</mixed-citation></citation-alternatives></ref><ref id="cit2"><label>2</label><citation-alternatives><mixed-citation xml:lang="ru">Clercq E.D. //J. clin. virol. – 2004. – V. 30. – P. 115-133.</mixed-citation><mixed-citation xml:lang="en">Clercq E.D. //J. clin. virol. – 2004. – V. 30. – P. 115-133.</mixed-citation></citation-alternatives></ref><ref id="cit3"><label>3</label><citation-alternatives><mixed-citation xml:lang="ru">Collin X., Sauleau A. //Bioorg. med. chem. letters. – 2003 – V. 13. – P. 2601-2605.</mixed-citation><mixed-citation xml:lang="en">Collin X., Sauleau A. //Bioorg. med. chem. letters. – 2003 – V. 13. – P. 2601-2605.</mixed-citation></citation-alternatives></ref><ref id="cit4"><label>4</label><citation-alternatives><mixed-citation xml:lang="ru">Papakonstantinou-Garoufalias S., Pouli N., Marakos P. //Formac. – 2002. – V. 57. – P. 973-977.</mixed-citation><mixed-citation xml:lang="en">Papakonstantinou-Garoufalias S., Pouli N., Marakos P. //Formac. – 2002. – V. 57. – P. 973-977.</mixed-citation></citation-alternatives></ref><ref id="cit5"><label>5</label><citation-alternatives><mixed-citation xml:lang="ru">Hester J.B., Rudzik A.D., Kamdar B.V. //J. med. chem. – 1971. – V 14. – P. 1078-1081.</mixed-citation><mixed-citation xml:lang="en">Hester J.B., Rudzik A.D., Kamdar B.V. //J. med. chem. – 1971. – V 14. – P. 1078-1081.</mixed-citation></citation-alternatives></ref><ref id="cit6"><label>6</label><citation-alternatives><mixed-citation xml:lang="ru">Thompson S.K., Eppley A.M., Frazer J.S. //Bioorg. med. chem. 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