“…Motivated by the above-mentioned results, numerous design and synthesis efforts have been employed to develop new derivatives with more effective and safer therapeutic profiles [15,16,17,18,19,20,21,22,23,24,25,26,27,28,29,30]. Additionally, heterocycles based on a thiazoline-2-thione core may undergo several chemical reactions, including alkylation, oxidation, and cycloaddition, as a result of having two different nitrogenous and sulfurous groups [31,32,33,34,35,36,37]. There are many methods for preparing thiazoline-2-thione derivatives from alkyl ammonium dithiocarbamates with the appropriate α-halocompound in the presence of an acid [38,39,40,41,42] or by using primary amines, CS 2 and α-haloketone in DMF [43] or toluene [44] or in water as a solvent [45], or without solvent or catalyst [46].…”