<?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>August 2009</publicationDate>
    <volume>5</volume>
    <issue>2</issue>
    <startPage>265</startPage>
    <endPage>270</endPage>
    <doi>juc</doi>
    <publisherRecordId>717</publisherRecordId>
    <documentType>article</documentType>
    <title language="eng">Synthesis of fluoro cinnolino (5, 4-C) pyrimidine compounds for antibacterial activity</title>
    <authors>
      <author>
        <name>MD. Shamim Ahmed</name>
        <affiliationId>1</affiliationId>
      </author>
      <author>
        <name>R.D. Hiremath</name>
        <affiliationId>1</affiliationId>
      </author>
      <author>
        <name>Farida Begum</name>
        <affiliationId>1</affiliationId>
      </author>
      <author>
        <name>Anurag Singh Mishra</name>
        <affiliationId>1</affiliationId>
      </author>
      <author>
        <name>J. Raghavendra</name>
        <affiliationId>1</affiliationId>
      </author>
      <author>
        <name>Shantharam U</name>
        <affiliationId>1</affiliationId>
      </author>
      <author>
        <name> L.V.G. Nargund (lvgnargund@rediffmail.com)</name>
        <affiliationId>1</affiliationId>
      </author>
    </authors>
    <affiliationsList>
      <affiliationName affiliationId="1">Department of Pharmaceutical Chemistry, Nargund College of Pharmacy, Dattatreyanagar, BSK III Stage, Bangalore- 85 Karnataka (INDIA)</affiliationName>
    </affiliationsList>
    <abstract language="eng">&lt;p style="text-align: justify;"&gt;In view of various biological activities of cinnoline derivatives like antibacterial, antioxidant, antineoplastic it was our interest to prepare fluoro-pyrimido-cinnolines and then substitute it with various anilines, morpholine, piperazine and to evaluate them for antimicrobial activity. Fluoro-pyrimido-cinnoline was synthesized by reaction between 4-fluoro-3-chloro-aniline with sodium nitrite in presence of conc. HCI to form diazonium salt solution. This on treatment with ethyl cyano-acetamide gives aryl-hydrazino(cyano)acetamide which reacts with chlorobenzene in the presence of AlCl&lt;sub&gt;3&lt;/sub&gt; to form 4-amino-3-cinnolino carboxamides which was further refluxed with formamide to give fluoro-pyrimido-cinnolines. Various fluoro-pyrimido-cinnoline derivatives were prepared by refluxing with morpholine, piperazine and substituted anilines in the presence of acetonitrile for 3-4 hours.&lt;/p&gt;&#xD;
</abstract>
    <fullTextUrl format="html">https://journalofchemistry.org/paper/717/</fullTextUrl>
    <keywords>
      <keyword language="eng">Synthesis of fluoro cinnolino</keyword>
    </keywords>
    <keywords>
      <keyword language="eng">pyrimidine compounds</keyword>
    </keywords>
    <keywords>
      <keyword language="eng">antibacterial activity</keyword>
    </keywords>
  </record>
</records>
