2019
DOI: 10.1002/jhet.3489
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New 1,3,4‐Thiadiazole Derivatives: Synthesis, Characterization, and Antimicrobial Activity

Abstract: In the present study, 2,5‐bis(mercapto‐acetichydrazide)‐1,3,4‐thiadiazole (1) was utilized by different reagents, namely, ethoxymethylene malononitrile, ethoxymethylene ethyl cyanoacetate, triethyl orthoformate, phenyl isothiocyanate, carbon disulfide, isatin, acetophenone, cyclohexanone, different aldehydes, and different anhydrides, to yield a new series of 2,5‐disubstituted‐1,3,4‐thiadiazoles 2–18. The chemical structure of these products was characterized by the spectral data IR, 1H‐NMR, 13C‐NMR, MS, and e… Show more

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Cited by 15 publications
(5 citation statements)
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“…It was then allowed to cool in ice water. The solid obtained (Compound III) was filtered and washed thoroughly with hot water then air dried [7][8][9]. The steps for the synthesis are highlighted from Fig.…”
Section: ) Step IIImentioning
confidence: 99%
“…It was then allowed to cool in ice water. The solid obtained (Compound III) was filtered and washed thoroughly with hot water then air dried [7][8][9]. The steps for the synthesis are highlighted from Fig.…”
Section: ) Step IIImentioning
confidence: 99%
“…The tested compounds exhibited higher to moderate activity in comparison with ceftriaxone at concentration 30 mg/discs. Compounds 14, 15, and 17 showed higher activity against bacteria E. coli, and compounds 15, 16, 17, and 18 showed higher activity against Enterococcus bacteria [50]. 1, 3, 4-thiadiazole-based thioglycosides were synthesized and evaluated for antimicrobial activity against several strains.…”
Section: Antibacterial and Antifungal Activitiesmentioning
confidence: 99%
“…The higher activity of the mentioned compounds is mainly due to the presence of Schiff bases, thiol groups, pyrazole rings, triazole rings, and imide rings within the structure of 1,3,4thiadiazole. 43 A series of novel N-(5-(ethylthio)-1,3,4-thiadiazol-2yl)-2-(5-methyl-6-thioxo-1,3,5-thiadiazinan-3yl)acetamide derivatives 50a-p (Scheme 26) were designed, synthesized and the antimicrobial activities of all the target compounds against Xanthomonas oryzae pv. oryzicola, X. oryzae pv.…”
Section: Therapeutic Studiesmentioning
confidence: 99%