2015
DOI: 10.1007/s11164-015-2200-5
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Green synthesis and evaluation of the antitumor activity of a novel series of 3-[4-bi-(4-fluorophenyl)methylpiperazinyl]-4-amino-5-thione-1,2,4-triazole Schiff bases

Abstract: Fourteen novel 1,2,4-triazole Schiff bases containing the 1-[bi-(4-fluorophenyl)methyl]piperazine group were prepared, in good yield (73-85 %), in five steps starting from 1-[bi-(4-fluorophenyl)methyl]piperazine and ethyl chloroacetate, with use of microwave irradiation. The structures of the new compounds were characterized by IR spectroscopy, MS, 1 H and 13 C NMR spectroscopy, and elemental analysis. Assay of the newly prepared compounds for bioactivity against tumor cells revealed that the most of the compo… Show more

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Cited by 12 publications
(4 citation statements)
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“…However, in case of refluxing of 4 H -1,2,4-triazole-3-thiol ( 268 ) with chloroacetic acid and different aldehydes or isatin derivatives in acidic media, various 5-substituted arylidene-thiazolotriazoles 269a – e in 49–68% yields or ( Z )-5-(1-acetyl-2-oxo-1 H -indol-3(2 H ,3 aH ,7 aH )-ylidene)thiazolo[3,2- b ]-1,2,4-triazol-6(5 H )-ones 270 were efficiently synthesized in 40% yield ( Scheme 78 ) [ 101 ]. Screening of the obtained compounds for anticancer activity revealed that 5-arylidene-[1,3]thiazolo[3,2- b ][1,2,4]triazol-6-ones 269a – e exhibited more potent anticancer activity than respective amides [ 101 ].…”
Section: Reactions Of 124-triazolethionesmentioning
confidence: 99%
“…However, in case of refluxing of 4 H -1,2,4-triazole-3-thiol ( 268 ) with chloroacetic acid and different aldehydes or isatin derivatives in acidic media, various 5-substituted arylidene-thiazolotriazoles 269a – e in 49–68% yields or ( Z )-5-(1-acetyl-2-oxo-1 H -indol-3(2 H ,3 aH ,7 aH )-ylidene)thiazolo[3,2- b ]-1,2,4-triazol-6(5 H )-ones 270 were efficiently synthesized in 40% yield ( Scheme 78 ) [ 101 ]. Screening of the obtained compounds for anticancer activity revealed that 5-arylidene-[1,3]thiazolo[3,2- b ][1,2,4]triazol-6-ones 269a – e exhibited more potent anticancer activity than respective amides [ 101 ].…”
Section: Reactions Of 124-triazolethionesmentioning
confidence: 99%
“…A high probability of finding a pharmacologically valuable substances among 1,2,4-triazoles and the broad possibilities for their chemical modifications are a solid foundation for the search for new synthetic drugs among them [5,6]. Compounds containing 1,2,4-triazole moiety have been demonstrated to have antimicrobial, antitumor, analgesic, hypolipidemic, neuroleptic and other kinds of activities [7][8][9][10][11][12]. Hence, the synthesis of new highly effective antimicrobial medicines containing this heterocyclic fragment is a promising branch in pharmaceutical chemistry investigations.…”
Section: Introductionmentioning
confidence: 99%
“…Протисудомна активність. Дослідниками [32] розглянуто регресійний аналіз, в якому як залежна змінна було виявлено протисудомну активність та обчислено дескриптори. Це дало моделі QSAR, точність та надійність, яка підтвердженна статистичними тестами.…”
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