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 <front>
  <journal-meta>
   <journal-id journal-id-type="publisher-id">From Chemistry Towards Technology Step-By-Step</journal-id>
   <journal-title-group>
    <journal-title xml:lang="en">From Chemistry Towards Technology Step-By-Step</journal-title>
    <trans-title-group xml:lang="ru">
     <trans-title>От химии к технологии шаг за шагом</trans-title>
    </trans-title-group>
   </journal-title-group>
   <issn publication-format="online">2782-1900</issn>
  </journal-meta>
  <article-meta>
   <article-id pub-id-type="publisher-id">83186</article-id>
   <article-id pub-id-type="doi">10.52957/27821900_2020_01_181</article-id>
   <article-categories>
    <subj-group subj-group-type="toc-heading" xml:lang="ru">
     <subject>Научные статьи</subject>
    </subj-group>
    <subj-group subj-group-type="toc-heading" xml:lang="en">
     <subject>Scientific articles</subject>
    </subj-group>
    <subj-group>
     <subject>Научные статьи</subject>
    </subj-group>
   </article-categories>
   <title-group>
    <article-title xml:lang="en">Synthesis of 3-cyanobenzen-1-sulfonyl chlorides</article-title>
    <trans-title-group xml:lang="ru">
     <trans-title>Synthesis of 3-cyanobenzen-1-sulfonyl chlorides</trans-title>
    </trans-title-group>
   </title-group>
   <contrib-group content-type="authors">
    <contrib contrib-type="author">
     <name-alternatives>
      <name xml:lang="ru">
       <surname>Агатьев</surname>
       <given-names>Павел Александрович</given-names>
      </name>
      <name xml:lang="en">
       <surname>Agat'ev</surname>
       <given-names>Pavel Aleksandrovich</given-names>
      </name>
     </name-alternatives>
     <xref ref-type="aff" rid="aff-1"/>
    </contrib>
    <contrib contrib-type="author">
     <name-alternatives>
      <name xml:lang="ru">
       <surname>Шленёв</surname>
       <given-names>Роман Михайлович</given-names>
      </name>
      <name xml:lang="en">
       <surname>Shlenev</surname>
       <given-names>Roman Mihaylovich</given-names>
      </name>
     </name-alternatives>
     <bio xml:lang="ru">
      <p>кандидат химических наук;</p>
     </bio>
     <bio xml:lang="en">
      <p>candidate of chemical sciences;</p>
     </bio>
     <xref ref-type="aff" rid="aff-2"/>
    </contrib>
    <contrib contrib-type="author">
     <name-alternatives>
      <name xml:lang="ru">
       <surname>Тарасов</surname>
       <given-names>Алексей Валерьевич</given-names>
      </name>
      <name xml:lang="en">
       <surname>Tarasov</surname>
       <given-names>Aleksey Valer'evich</given-names>
      </name>
     </name-alternatives>
     <bio xml:lang="ru">
      <p>доктор химических наук;</p>
     </bio>
     <bio xml:lang="en">
      <p>doctor of chemical sciences;</p>
     </bio>
     <xref ref-type="aff" rid="aff-3"/>
    </contrib>
    <contrib contrib-type="author">
     <name-alternatives>
      <name xml:lang="ru">
       <surname>Рыбина</surname>
       <given-names>Галина Викторовна</given-names>
      </name>
      <name xml:lang="en">
       <surname>Rybina</surname>
       <given-names>Galina Viktorovna</given-names>
      </name>
     </name-alternatives>
     <bio xml:lang="ru">
      <p>кандидат химических наук;</p>
     </bio>
     <bio xml:lang="en">
      <p>candidate of chemical sciences;</p>
     </bio>
     <xref ref-type="aff" rid="aff-3"/>
    </contrib>
   </contrib-group>
   <aff-alternatives id="aff-1">
    <aff>
     <institution xml:lang="ru">АО “Химтраст”</institution>
     <country>Россия</country>
    </aff>
    <aff>
     <institution xml:lang="en">АО “Химтраст”</institution>
     <country>Russian Federation</country>
    </aff>
   </aff-alternatives>
   <aff-alternatives id="aff-2">
    <aff>
     <institution xml:lang="ru">ООО “Технология лекарств”</institution>
     <country>Россия</country>
    </aff>
    <aff>
     <institution xml:lang="en">ООО “Технология лекарств”</institution>
     <country>Russian Federation</country>
    </aff>
   </aff-alternatives>
   <aff-alternatives id="aff-3">
    <aff>
     <institution xml:lang="ru">Ярославский государственный технический университет</institution>
    </aff>
    <aff>
     <institution xml:lang="en">Yaroslavl State Technical University</institution>
    </aff>
   </aff-alternatives>
   <pub-date publication-format="print" date-type="pub" iso-8601-date="2020-12-31T00:00:00+03:00">
    <day>31</day>
    <month>12</month>
    <year>2020</year>
   </pub-date>
   <pub-date publication-format="electronic" date-type="pub" iso-8601-date="2020-12-31T00:00:00+03:00">
    <day>31</day>
    <month>12</month>
    <year>2020</year>
   </pub-date>
   <volume>1</volume>
   <issue>1</issue>
   <fpage>181</fpage>
   <lpage>189</lpage>
   <history>
    <date date-type="received" iso-8601-date="2020-09-15T00:00:00+03:00">
     <day>15</day>
     <month>09</month>
     <year>2020</year>
    </date>
    <date date-type="accepted" iso-8601-date="2020-10-20T00:00:00+03:00">
     <day>20</day>
     <month>10</month>
     <year>2020</year>
    </date>
   </history>
   <self-uri xlink:href="https://chemintech.ru/en/nauka/article/83186/view">https://chemintech.ru/en/nauka/article/83186/view</self-uri>
   <abstract xml:lang="ru">
    <p>The paper presents a preparation method for 3-cyanobenzene-1-sulfonyl chlorides, valuable reagents for the fine organic synthesis used in the preparation of antiplatelet agents and agricultural germicides, pharmaceutical compositions, and biologically active compounds.</p>
   </abstract>
   <trans-abstract xml:lang="en">
    <p>The paper presents a preparation method for 3-cyanobenzene-1-sulfonyl chlorides, valuable reagents for the fine organic synthesis used in the preparation of antiplatelet agents and agricultural germicides, pharmaceutical compositions, and biologically active compounds.</p>
   </trans-abstract>
   <kwd-group xml:lang="en">
    <kwd>preparation method</kwd>
    <kwd>3-cyanobenzene-1-sulfonyl chlorides</kwd>
    <kwd>antiplatelet agents</kwd>
    <kwd>agricultural germicides</kwd>
   </kwd-group>
  </article-meta>
 </front>
 <body>
  <p></p>
 </body>
 <back>
  <ref-list>
   <ref id="B1">
    <label>1.</label>
    <citation-alternatives>
     <mixed-citation xml:lang="ru">Perzborn E., Seuter F., Fruchtmann R., Kohlsdorfer C. Substituted phenyl-sulphon amides. Patent No. DE3632329(A1) Germany. No. 19863632329, publ. 31.03.1988.</mixed-citation>
     <mixed-citation xml:lang="en">Perzborn E., Seuter F., Fruchtmann R., Kohlsdorfer C. Substituted phenyl-sulphon amides. Patent No. DE3632329(A1) Germany. No. 19863632329, publ. 31.03.1988.</mixed-citation>
    </citation-alternatives>
   </ref>
   <ref id="B2">
    <label>2.</label>
    <citation-alternatives>
     <mixed-citation xml:lang="ru">Igarashi K., Enomoto Y., Yanagida H., Gohara M., Iida N., Ozawa S., Kuwazuka T. Sulfonamide based compound and agricultural germicide. Patent No. JPH0655708 (B2) Japan. No. 19850099595, publ. 27.07.1994.</mixed-citation>
     <mixed-citation xml:lang="en">Igarashi K., Enomoto Y., Yanagida H., Gohara M., Iida N., Ozawa S., Kuwazuka T. Sulfonamide based compound and agricultural germicide. Patent No. JPH0655708 (B2) Japan. No. 19850099595, publ. 27.07.1994.</mixed-citation>
    </citation-alternatives>
   </ref>
   <ref id="B3">
    <label>3.</label>
    <citation-alternatives>
     <mixed-citation xml:lang="ru">Witte E.-C., Stegmeier K., Doerge L. Sulfonamidoalkyl cycloalkane compounds, processes for their production and pharmaceutical preparations. Patent No. DE3829455(A1) Germany. No. 19883829455, publ. 15.03.1990.</mixed-citation>
     <mixed-citation xml:lang="en">Witte E.-C., Stegmeier K., Doerge L. Sulfonamidoalkyl cycloalkane compounds, processes for their production and pharmaceutical preparations. Patent No. DE3829455(A1) Germany. No. 19883829455, publ. 15.03.1990.</mixed-citation>
    </citation-alternatives>
   </ref>
   <ref id="B4">
    <label>4.</label>
    <citation-alternatives>
     <mixed-citation xml:lang="ru">Witte E.-C., Stegmeier K., Dorge L., Doerge, L. Sulfonamidoalkyl cycloalkane compounds, processes for their production and pharmaceutical preparations. Patent No. EP0361113 (B1) Europe. No. 19890115912, publ. 07.07.1993.</mixed-citation>
     <mixed-citation xml:lang="en">Witte E.-C., Stegmeier K., Dorge L., Doerge, L. Sulfonamidoalkyl cycloalkane compounds, processes for their production and pharmaceutical preparations. Patent No. EP0361113 (B1) Europe. No. 19890115912, publ. 07.07.1993.</mixed-citation>
    </citation-alternatives>
   </ref>
   <ref id="B5">
    <label>5.</label>
    <citation-alternatives>
     <mixed-citation xml:lang="ru">Owa T., Yoshino H., Okauchi T., et al. J. Med. Chem. 1999. V. 42. N. 19. P. 3789-3799.</mixed-citation>
     <mixed-citation xml:lang="en">Owa T., Yoshino H., Okauchi T., et al. J. Med. Chem. 1999. V. 42. N. 19. P. 3789-3799.</mixed-citation>
    </citation-alternatives>
   </ref>
   <ref id="B6">
    <label>6.</label>
    <citation-alternatives>
     <mixed-citation xml:lang="ru">Wakabayashi T., Ono N., Semba T., Haneda T. Antitumor agent comprising combination of sulfonamide-containing heterocyclic compound with an angiogenesis inhibitor. Patent No. US2005119303 (A1) USA. No. 20040504676, publ. 02.06.2005.</mixed-citation>
     <mixed-citation xml:lang="en">Wakabayashi T., Ono N., Semba T., Haneda T. Antitumor agent comprising combination of sulfonamide-containing heterocyclic compound with an angiogenesis inhibitor. Patent No. US2005119303 (A1) USA. No. 20040504676, publ. 02.06.2005.</mixed-citation>
    </citation-alternatives>
   </ref>
   <ref id="B7">
    <label>7.</label>
    <citation-alternatives>
     <mixed-citation xml:lang="ru">Mrozik H. Anthelmintic substituted sulfonamide derivatives: Application US3953492 (A) USA. No. 19750562712, publ. 27.04.1976.</mixed-citation>
     <mixed-citation xml:lang="en">Mrozik H. Anthelmintic substituted sulfonamide derivatives: Application US3953492 (A) USA. No. 19750562712, publ. 27.04.1976.</mixed-citation>
    </citation-alternatives>
   </ref>
   <ref id="B8">
    <label>8.</label>
    <citation-alternatives>
     <mixed-citation xml:lang="ru">Hagmann W., Lin L., Liu P., Mumford R., Reger T., Smith N., Stock N., Zunic J. Vla-4 antagonists. Patent No. US2007179190 (A1) USA. No. 20050591820, publ. 02.08.2007.</mixed-citation>
     <mixed-citation xml:lang="en">Hagmann W., Lin L., Liu P., Mumford R., Reger T., Smith N., Stock N., Zunic J. Vla-4 antagonists. Patent No. US2007179190 (A1) USA. No. 20050591820, publ. 02.08.2007.</mixed-citation>
    </citation-alternatives>
   </ref>
   <ref id="B9">
    <label>9.</label>
    <citation-alternatives>
     <mixed-citation xml:lang="ru">Reger T.S., Zunic J., Stock N., et al.  Bioorg. Med. Chem. Lett. 2010. V. 20. N. 3. P. 1173–1176.</mixed-citation>
     <mixed-citation xml:lang="en">Reger T.S., Zunic J., Stock N., et al.  Bioorg. Med. Chem. Lett. 2010. V. 20. N. 3. P. 1173–1176.</mixed-citation>
    </citation-alternatives>
   </ref>
   <ref id="B10">
    <label>10.</label>
    <citation-alternatives>
     <mixed-citation xml:lang="ru">Aldrich Chemistry 2012-2014: Handbook of Fine Chemicals. Sigma-Aldrich, 2011. P. 3216.</mixed-citation>
     <mixed-citation xml:lang="en">Aldrich Chemistry 2012-2014: Handbook of Fine Chemicals. Sigma-Aldrich, 2011. P. 3216.</mixed-citation>
    </citation-alternatives>
   </ref>
   <ref id="B11">
    <label>11.</label>
    <citation-alternatives>
     <mixed-citation xml:lang="ru">Gilbert E.E. Sulfonation and related reactions. New York: Interscience Publishers, 1965. 529 p.</mixed-citation>
     <mixed-citation xml:lang="en">Gilbert E.E. Sulfonation and related reactions. New York: Interscience Publishers, 1965. 529 p.</mixed-citation>
    </citation-alternatives>
   </ref>
   <ref id="B12">
    <label>12.</label>
    <citation-alternatives>
     <mixed-citation xml:lang="ru">Cremlyn R.J. Chlorosulfonic acid: A versatile reagent. RSC Publishing, 2002. 322 p.</mixed-citation>
     <mixed-citation xml:lang="en">Cremlyn R.J. Chlorosulfonic acid: A versatile reagent. RSC Publishing, 2002. 322 p.</mixed-citation>
    </citation-alternatives>
   </ref>
   <ref id="B13">
    <label>13.</label>
    <citation-alternatives>
     <mixed-citation xml:lang="ru">Malet-Sanz L., Madrzak J., Ley S.V. Preparation of arylsulfonyl chlorides by chlorosulfonylation of in situ generated diazonium salts using a continuous flow reactor. Org. Biomol. Chem. 2010. N. 8. P. 5324-5332.</mixed-citation>
     <mixed-citation xml:lang="en">Malet-Sanz L., Madrzak J., Ley S.V. Preparation of arylsulfonyl chlorides by chlorosulfonylation of in situ generated diazonium salts using a continuous flow reactor. Org. Biomol. Chem. 2010. N. 8. P. 5324-5332.</mixed-citation>
    </citation-alternatives>
   </ref>
   <ref id="B14">
    <label>14.</label>
    <citation-alternatives>
     <mixed-citation xml:lang="ru">Tarasov A.V., Moskvichev Ju.A., Pisarev P.K., Nikiforova A.A. Method for preparing arylchlorosulfonyl benzamides from benzoic acids. Invention Patent No. RU2298548C1, 10.05.2007.</mixed-citation>
     <mixed-citation xml:lang="en">Tarasov A.V., Moskvichev Ju.A., Pisarev P.K., Nikiforova A.A. Method for preparing arylchlorosulfonyl benzamides from benzoic acids. Invention Patent No. RU2298548C1, 10.05.2007.</mixed-citation>
    </citation-alternatives>
   </ref>
   <ref id="B15">
    <label>15.</label>
    <citation-alternatives>
     <mixed-citation xml:lang="ru">Comprehensive organic chemistry: The synthesis and reactions of organic compounds. A series of 6 volumes.  Edited by D. Barton and W.D. Ollis. Volume 2. Nitrogen Compounds. Pergamon Press. 1979.</mixed-citation>
     <mixed-citation xml:lang="en">Comprehensive organic chemistry: The synthesis and reactions of organic compounds. A series of 6 volumes.  Edited by D. Barton and W.D. Ollis. Volume 2. Nitrogen Compounds. Pergamon Press. 1979.</mixed-citation>
    </citation-alternatives>
   </ref>
   <ref id="B16">
    <label>16.</label>
    <citation-alternatives>
     <mixed-citation xml:lang="ru">Harrison I.T., Harrison S. Compendium of organic synthetic methods. John Wiley &amp; Sons, Inc. 1971. 529 p.</mixed-citation>
     <mixed-citation xml:lang="en">Harrison I.T., Harrison S. Compendium of organic synthetic methods. John Wiley &amp; Sons, Inc. 1971. 529 p.</mixed-citation>
    </citation-alternatives>
   </ref>
  </ref-list>
 </back>
</article>
