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  <front>
    <journal-meta>
      <journal-title-group>
        <journal-title>American Journal of PharmTech Research</journal-title>
        <abbrev-journal-title abbrev-type="publisher">AJPTR</abbrev-journal-title>
      </journal-title-group>
      <issn pub-type="epub">2249-3387</issn>
      <publisher>
        <publisher-name>undefined</publisher-name>
      </publisher>
    </journal-meta>
    <article-meta>
      <article-id pub-id-type="publisher-id">AJPTR34049</article-id>
      <title-group>
        <article-title>Synthesis and Antimicrobial Activity of Piperazine Derivatives</article-title>
      </title-group>
      <contrib-group>
        <contrib contrib-type="author">
          <name>
            <surname>M</surname>
            <given-names>Somashekhar</given-names>
          </name>
        </contrib>
        <contrib contrib-type="author">
          <name>
            <surname>AR</surname>
            <given-names>Mahesh</given-names>
          </name>
        </contrib>
      </contrib-group>
      <pub-date pub-type="epub" iso-8601-date="2013-08-01">
        <month>08</month>
        <day>01</day>
        <year>2013</year>
      </pub-date>
      <volume>3</volume>
      <issue>4</issue>
      <abstract>
        <p>Ethyl piperazine is treated with 4- chloro nitrobenzene in presence of anhydrous potassium carbonate and methanol is used as a solvent forms 1 ethyl -4-[4-nitrophenyl] piperazine, then it is treated with iron dust in presence of hydrochloric acid and neutralized with sodium carbonate to form the 4-[4-ethyl piperazine-1-yl] anilline, it is reacted with n-chloro acetyl aryl amine in presence of  anhydrous potassium carbonate forms the final product  1-[2-(aryl amino -2-oxoethyl ) - amino -4-(n-ethyl piperazine)] benzene derivatives were synthesized, the synthesized compounds were screened for their antibacterial activates against s. aures and e.coli by cup plates method . From screening results of some compounds found highly active against both gram – positive and gram – negative bacteria while other compounds possess moderate activity.</p>
      </abstract>
      <kwd-group kwd-group-type="author">
        <kwd>Ethyl Piperazine</kwd>
        <kwd>Potassium Carbonate</kwd>
        <kwd>N-Chloro Acetyl Aryl Amine.</kwd>
      </kwd-group>
    </article-meta>
  </front>
  <body>
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