<?xml version="1.0"?>
<records>
  <record>
    <language>eng</language>
    <publisher>Ansari Education and Research Society</publisher>
    <journalTitle>Journal of Ultra Chemistry</journalTitle>
    <issn>0973-3450</issn>
    <eissn>2319-8036</eissn>
    <publicationDate>December 2008</publicationDate>
    <volume>4</volume>
    <issue>2</issue>
    <startPage>189</startPage>
    <endPage>194</endPage>
    <doi>juc</doi>
    <publisherRecordId>729</publisherRecordId>
    <documentType>article</documentType>
    <title language="eng">Synthesis of 2-imino-4-oxo-thiazolidino based quinoxalinediones as antitubercular agents </title>
    <authors>
      <author>
        <name>P.Y. PAWAR</name>
        <affiliationId>1</affiliationId>
      </author>
      <author>
        <name>S.B. BHISE</name>
        <affiliationId>2</affiliationId>
      </author>
    </authors>
    <affiliationsList>
      <affiliationName affiliationId="1">P.D.V.V.P. Fs, College of Pharmacy, Post MIDC, Vilad Ghat, Ahmednagar - 414 111, (MS) INDIA</affiliationName>
      <affiliationName affiliationId="2">Government College of Pharmacy, Karad - 415 124 (MS) INDIA</affiliationName>
    </affiliationsList>
    <abstract language="eng">&lt;p style="text-align: justify;"&gt;6,7-bis[3-(4-substitutedphenyl)-4-oxo-thiazolidin-2-ylideneamino] quinoxa line-2,3(1&lt;em&gt;H&lt;/em&gt;,4&lt;em&gt;H&lt;/em&gt;)-diones &lt;strong&gt;(3a-e)&lt;/strong&gt; have been synthesized by cyclisation of 6,7-bis[3&amp;#39;-aryl thiocarbamido]-quinoxaline-2,3(1&lt;em&gt;H&lt;/em&gt;, 4&lt;em&gt;H&lt;/em&gt;)-diones &lt;strong&gt;(2a-e)&lt;/strong&gt; in presence of mono-chloroacetic acid, sodium acetate and glacial acetic acid. 6,7-Bis[3&amp;#39;-aryl thiocarbamido]-quinoxaline-2,3(1&lt;em&gt;H&lt;/em&gt;,4&lt;em&gt;H&lt;/em&gt;) -diones were obtained by reaction of 6,7-diaminoquinoxaline-2,3(1&lt;em&gt;H&lt;/em&gt;,4&lt;em&gt;H&lt;/em&gt;)-dione with substituted aromatic isothiocyanate. The constitution of the synthesized compounds is supported by IR, &lt;sup&gt;1&lt;/sup&gt;H NMR, Mass and elemental analysis. The compounds were subjected to preliminary &lt;em&gt;in-vitro&lt;/em&gt; evaluation for antitubercular activity against &lt;em&gt;Mycobacterium tuberculosis&lt;/em&gt; H&lt;sub&gt;37&lt;/sub&gt;RV strain.&lt;br /&gt;&#xD;
&amp;nbsp;&lt;/p&gt;&#xD;
</abstract>
    <fullTextUrl format="html">https://journalofchemistry.org/paper/729/</fullTextUrl>
    <keywords>
      <keyword language="eng">Quinoxaline-2</keyword>
    </keywords>
    <keywords>
      <keyword language="eng">antitubercular activity</keyword>
    </keywords>
  </record>
</records>
