Affiliation:
1. Roland Institute of Pharmaceutical Sciences (Biju Patnaik University of Technology Nodal Centre of Research), Berhampur,
760010, India
2. Department of Mathematics and Natural Sciences, College of Sciences and Human Studies,
Prince Mohammad Bin Fahd University, Al Khobar, 31952, Saudi Arabia
3. Pharmacy Academy, IFTM University, Lodhipur
Rajput, Moradabad, Uttar Pradesh, 244102, India
4. Department of Chemistry, Kanak Manjari Institute of Pharmaceutical
Sciences, Rourkela, Odisha, 769015, India
Abstract
Abstract:
Thiadiazole is a paradigm of five membered heterocyclic compound that contains two
nitrogens and one sulphur as heteroatoms with molecular formula C2H2N2S. Thiadiazole is mainly
present in four isomeric forms such as 1,2,3-thiadiazole, 1,2,4-thiadiazole, 1,2,5-thiadiazole and
1,3,4-thiadiazole. Out of these isomers, 1,3,4-thiadiazole has attracted remarkable attention in the
field of medicinal chemistry. Some of the drugs containing 1,3,4-thiadiazole moiety are used clinically
and are available in the market including Sulphamethizole (Antibacterial), Acetazolamide
(Diuretic), Azetepa (Antineoplastic), Cefazolin (Antibiotic), Megazol (Antiprotozoal), Atibeprone
(anti-depressant). Several greener approaches are applied for the synthesis of thiadiazole scaffolds
including microwave irradiation, ultrasonic irradiation, grinding, ball milling technique, etc. These
methods are eco-friendly, nonhazardous, reproducible, and economical approach. Based on these
Green chemistry approaches, thiadiazole derivatives are synthesized from thiosemicarbazide. The
functionalization of these heterocyclic compounds generates thiadiazole derivatives with diverse
chemical structures. This review covers green synthesis, biological potentials, and structure activity
relationship study of thiadiazole analogs.
Publisher
Bentham Science Publishers Ltd.
Subject
Organic Chemistry,Analytical Chemistry,Catalysis