In the present work, compound 3-arylidene amino-5-methyl-1,2,4-triazole (IIIa-c), required as starting material obtained in one-pot reaction by condensing 5-methyl-3-amino-1,2,4-triazole with different aromatic aldehydes. The required 5-methyl-3-amino-1,2,4-triazole was prepared from treatment of acetyl urea (I) with hydrazine hydrate, the compounds (IIIa-c) were converted to the corresponding [3-[5-methyl-1,2,4-triazol-2-yl]-2-arylthiazolidine-4-one (Va1-a3) and imidazoleine-4-one (Vb1-b3) by reacted it with thioglycolic acid and Glycine in absolute ethanol. The compounds (IIa-c) were converted also to 2-methyl-5-arylamino-5,6,-dihydroimidozo[2,1-b]-1,2,4-triazole (VIIIa-VIIIc) reacted with TCA then with aniline derivatives. The linear pathway strategy of all these synthesized compounds can be summarized in scheme (1).
Bhimagouda S. PatilG. KrishnamurthyNellisara D. ShashikumarM. R. LokeshH. S. Bhojya Naik
P. Prashanth Babu1*, P. Upendra2, D. Venkateshwar Rao3
NESLİHAN DEMİRBAŞA. DemirbaşHacer BayrakHakan BektaşŞengül Alpay Karaoğlu
Yatin J. MangeArun M. IsloorShridhar MalladiShrikrishna IsloorHoong‐Kun Fun