1318-1324A series of novel <span style="mso-bidi-font-weight:
bold">hybrid 2-(7-chloroquinolin-4-ylthio)-5-(substituted)-1,3,4-oxadiazole derivatives have been designed,
synthesized which contains different pharmacophores like quinoline and
1,3,4-oxadiazole linked via sulfur atom. All the newly synthesized derivatives
have been characterized by IR, 1H NMR, 13C NMR spectral
and elemental analysis. Further, All the final synthesized scaffolds have been
subjected to in vitro antimicrobial
activity against several bacteria (E.coli<span style="mso-bidi-font-weight:
bold">, P.aeruginosa,
S.aureus, S.pyogenus) and fungi (C.albicans,
A.niger, A.clavatus) using
broth dilution technique. Among the compounds tested, compounds 3f substituted with coumarin analogue
and 3b with amine group at second
position of phenyl to oxadiazole moiety are found to be most potent.
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