Hydroxybenzophenones. -Hitherto unknown triazolothiadiazine derivatives (IX) are synthesized and evaluated for their antimicrobial activity. Almost all the novel heterocycles show higher antibacterial effects compared to the standard drug chloramphenicol. Moreover, halo-substituted derivatives exhibit antifungal activity higher than that of the reference compound, fluconazole, against F. moniliforme and C. gloeosporioides. -(KHANUM, S. A.; SHASHIKANTH*, S.; UMESHA, S.; KAVITHA, R.; Eur.
Several 1-benzhydryl-sulfonyl-4-(3-(piperidin-4-yl)propyl)piperidine derivatives 8(a-j) were prepared by the treatment of substituted benzhydryl chlorides with 4-(3-(piperidin-4-yl)propyl)piperidine followed by N-sulfonation with sulfonyl chlorides in the presence of dry methylene dichloride and triethyl amine. The synthesized compounds were characterized by (1)H-NMR, IR, and elemental analysis. All the synthesized compounds were evaluated in vitro for their efficacy as antimicrobial agents by artificial inoculation technique against standard strains of two important bacterial viz., Xanthomonas axonopodis pv. vesicatoria and Ralstonia solanacearum as well as and two fungal pathogens namely Alternaria solani and Fusarium solani of tomato plants. We have briefly investigated the structure-activity relation studies and reveal that the nature of substitutions on benzhydryl ring and sulfonamide ring influences the antibacterial activity. Among the synthesized new compounds 8b, 8d, 8g, 8h, 8i, and 8j were showed significant potent antimicrobial activities compared to the standard drugs chloramphenicol, mancozeb.
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