synthesis of some oxadiazole derivatives as new anticandidal agents合成一些oxadiazole衍生品新anticandidal代理.pdf
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Molecules 2011, 16, 7662-7671; doi:10.3390/molecule
OPEN ACCESS
molecules
ISSN 1420-3049
/journal/molecules
Article
Synthesis of Some Oxadiazole Derivatives as
New Anticandidal Agents
Zafer Asim Kaplancikli
Department of Pharmaceutical Chemistry, Faculty of Pharmacy, Anadolu University, 26470 Eskişehir,
Turkey; E-Mail: zakaplan@.tr; Tel.: +90-222-3350580/3776; Fax: +90-222-3350750
Received: 25 July 2011; in revised form: 23 August 2011 / Accepted: 6 September 2011 /
Published: 7 September 2011
Abstract: In this study, 5-[(pyrimidin-2-ylthio)methyl]-1,3,4-oxadiazole-2(3H)-thione (3)
was synthesized via the ring closure reaction of 2-(pyrimidin-2-ylthio)acetohydrazide (2)
with carbon disulphide. New oxadiazole derivatives 4a-f were obtained by the nucleophilic
substitution reaction of compound 3 with various phenacyl bromides. The chemical
1 13 +
structures of the compounds were elucidated by IR, H-NMR, C-NMR and FAB -MS
spectral data and elemental analyses. The newly synthesized derivatives 4a-f were tested in
vitro by using a microbroth dilution method against C. albicans (clinical isolate,
Osmangazi University, Faculty of Medicine, Eskişehir, Turkey), C. albicans (ATCC
90028), C. g
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