Paper Title
Design and synthesis of oxadiazole derivatives based on 2-Mercaptobenzimidazole
Article Identifiers
Registration ID: IJNRD_186933
Published ID: IJNRD2302082
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Keywords
Organic Chemistry, Oxadiazole, and 2-Mercaptobenzimidazole
Abstract
In the present work, novel oxadiazole derivatives of 2-mercaptobenzimidazole were synthesized following standard multistep synthetic pathways. Synthetic organic chemistry is concerned with the shaping of new organic compound from preexisting precursor. The present work was aimed to obtain a number of Schiff bases from benzimidazole hetrocycle. 2-MBI was modified using analytical grade reagents and solvents and the results obtained were satisfactory and parallel with the standard procedures of the laboritories.2-MBI was converted to thioether which was then converted to respective ester, hydrazide and finally to imine derivatives called Schiff Bases.The Schiff bases obtained may be used in a number of ways for example as a complexing agent and precursor of a number of compounds in future. These derivatives have large applications in various fields, such as organometallics, agriculture, medicinal, industrial, explosives, polymers and petrochemicals The products were obtained in good yields and purity. Furthure oxadiazoles may be synthesized using different carbonyl compounds. This work may be utilized in future for derivation of potential medicinal agents. The bio activity of the synthesized compounds may be conducted for establishing the medicinal property of these compounds.
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How To Cite (APA)
Siraj & Omer Dad (February-2023). Design and synthesis of oxadiazole derivatives based on 2-Mercaptobenzimidazole . INTERNATIONAL JOURNAL OF NOVEL RESEARCH AND DEVELOPMENT, 8(2), a663-a682. https://ijnrd.org/papers/IJNRD2302082.pdf
Issue
Volume 8 Issue 2, February-2023
Pages : a663-a682
Other Publication Details
Paper Reg. ID: IJNRD_186933
Published Paper Id: IJNRD2302082
Research Area: Science & Technology
Author Type: Foreign Author
Country: Mansehra, Pakistan, Pakistan
Published Paper PDF: https://ijnrd.org/papers/IJNRD2302082.pdf
Published Paper URL: https://ijnrd.org/viewpaperforall?paper=IJNRD2302082
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