1995
DOI: 10.1515/dmdi.1995.12.2.145
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Synthesis and Antimicrobial Activity of Some New 1-[4-(4-Fluorobenzoylamino) Benzoyl)-4-Substituted Thiosemicarbazides

Abstract: 1-Aroyl-4-substituted thiosemicarbazides were obtained by the addition of 4-(4-fluorobenzoylamino)benzoylhydrazine to methyl, ethyl, propyl, allyl, cyclohexyl, phenyl and phenethyl isothiocyanates. The structures of the synthesized compounds were confirmed using UV, IR, 1H-NMR (for compounds 4c, 4g) and mass (for compounds 4b, 4c, 4g) spectral methods together with elemental analyses. None of the synthesized compounds has been reported previously.

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Cited by 5 publications
(3 citation statements)
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“…Refluxing compound 1 (commercial phenylacetohydrazide), and compound 2 (Ibuprofen hydrazide) with methyl-/ethylisothiocyanate in ethanol yielded substituted thiosemicarbazides (compounds 3-6, Figs. S5-S15) [25,[35][36][37][38][39][40][41][42][43][44][45]. All cyclization products (compound 7-10, Figs.…”
Section: Chemistrymentioning
confidence: 99%
“…Refluxing compound 1 (commercial phenylacetohydrazide), and compound 2 (Ibuprofen hydrazide) with methyl-/ethylisothiocyanate in ethanol yielded substituted thiosemicarbazides (compounds 3-6, Figs. S5-S15) [25,[35][36][37][38][39][40][41][42][43][44][45]. All cyclization products (compound 7-10, Figs.…”
Section: Chemistrymentioning
confidence: 99%
“…N 1 , N 2 and N 4 protones which prove the presence of thiosemicarbazides were detected in 1 H-NMR spectrum (Fig 3) and the information given is supported by the literature. (17)(18)(19)(20)(21)(22). 4c, 4e, 4f, 4h), it was determined that these compounds undergo thione-thiol tautomerism (Fig 4).…”
Section: Synthesis Of Tolmetin Thiosemicarbazidesmentioning
confidence: 99%
“…Therefore, the thiosemicarbazide is a highly efficient pharmacophore in molecular design. On the other hand, various derivatives of thiosemicarbazide have been reported to possess interesting biological activities such as antimicrobial (58), anticonvulsant (9), antibacterial (1012), antifungal (13–17), anti-inflammatory (18,19) antiviral (20) and anticancer activities (2124). In this study, we have explored the therapeutic potential of the thiosemicarbazide scaffold against HCV NS5B.…”
Section: Introductionmentioning
confidence: 99%