“…Despite this, 1,3,4-oxadiazoles were found to be the medicinate backbone in the number of therapeutic agents (Lam et al, 2010), such as fenadiazole [4] (hypnotic drug), raltegravir [5] (anti HIV drug), furamizole [6] (antibacterial agent), BB-83698 (potent PDF inhibitor), tiodazosin (antihypertensive drug), nesapidil [7] (antiarrhythemic drug), Zibotentan (Oliveira et al, 2012) (ZD4054) [8] (anticancer agent) and pleconaril [9] (antiviral drug). These 1,3,4-oxadiazoles can be synthesized from different methods such as from the reaction of substituted propanoic acid and alkyl/aryl hydrazide, which undergo cyclization to give 1,3,4-oxadiazoles in the presence of POCl 3 (Somani and Shirodkar, 2009), and several other synthetic pathways are reported for the synthesis of 1,3,4-oxadiazoles (Husain and Ajmal, 2009 Both of the rings are very important pharmacophore in modern drug discovery, because both possess a number of biological (anticonvulsant and antimicrobial) activities (Bin et al, 1998). These derivatives were also synthesized by the microwave assisted method (Jha et al, 2010, Rashid et al, 2012 from aromatic acid and trichloroacetic acid.…”