Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/16448
Title: Synthesis of 2, 5-disubstituted 1, 3, 4-oxadiazoles as biologically active heterocycles
Authors: Kagthara, Preeti R
Shah, Niraj S
Doshi, Rajeev K
Parekh, H H
Issue Date: May-1999
Publisher: NISCAIR-CSIR, India
Abstract: 2-(8enzimidazol-2'-yl) benzoyl hydrazide 1 when condensed with aromatic acids in the presence of POCI3 afforded 2-aryl -5-[2'-benzimidazol-2"-yl) phenyl]-l, 3, 4-oxadiazoles 2a-o. The acid hydrazide 1 on cyclisation with CNBr yield 2-amino-5-[2'-(benzimidazol-2 "-yl-phenyl)- 1, 3, 4-oxadiazole 3 which on reaction with aryl sulphonyl chlorides and substituted benzoyl chloride give the corresponding sulphonaillides 4a-o and amides 5a-o, respectively. All the products have been evaluated in vitro for their antimicrobial activity against several microbes and antitubercular activity against Mycobacterium tuberculosis H37Rv.
Page(s): 572-576
Appears in Collections:IJC-B Vol.38B(05) [May 1999]

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