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REVISTA DE CHIMIE
Cite as: Rev. Chim.
https://doi.org/10.37358/Rev.Chim.1949

OSIM Nr. R102355
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Revista de Chimie (Rev. Chim.), Year 2010, Volume 61, Issue 2,





STEFANIA-FELICIA BARBUCEANU, GABRIELA BANCESCU, OLGA DANIELA CRETU, CONSTANTIN DRAGHICI, ADRIAN BANCESCU, MANUELA RADU-POPESCU
New Heterocyclic Compounds from 1,3,4-Thiadiazole,
1,3,4-Oxadiazole and 1,2,4-Triazole Class
with Potential Antibacterial Activity

Abstract:

In this paper new heterocyclic compounds from 2-amino-1,3,4-thiadiazole, 2-amino-1,3,4-oxadiazole and 1,2,4-triazol-3(4H)-thione class were obtained from acylthiosemicarbazide 2 by intramolecular cyclization in different conditions. In the reaction of 4-(4-bromophenylsulfonyl)-benzoic acid hydrazide 1 with 4-fluorophenyl isothiocyanate, the new 1-[4-(4-bromophenylsulfonyl)benzoyl]-4-(4-fluorophenyl)-thiosemi-carbazide 2 was obtained. 5-(4-(4-Bromophenylsulfonyl)phenyl)-N-(4-fluorophenyl)-1,3,4-thiadiazol-2-amine 3 was prepared by the intramolecular cyclization of acylthiosemicarbazide 2 in concentrated sulphuric acid media. 5-(4-(4-Bromophenylsulfonyl)phenyl)-N-(4-fluorophenyl)-1,3,4-oxadiazol-2-amine 4 was obtained from reaction of acylthiosemicarbazide 2 with HgO, in alcoholic media, or with I2/KI, in basic media. The synthesis of 5-(4-(4-bromophenylsulfonyl)phenyl)-4-(4-fluorophenyl)-2H-1,2,4-triazole-3(4H)-thione 5 was carried out by cyclodehydration of acylthiosemicarbazide 2 in sodium hydroxide media. Alkylation of 1,2,4-triazole 5 with ethyl bromoacetate afforded S-substituted 1,2,4-triazole 6. Acylation of same 1,2,4-triazole 5 with acetyl chloride led to the N-substituted 1,2,4-triazole 7. The structures of these new compounds were elucidated by FTIR, UV-Vis, 1H-NMR, 13C-NMR, MS spectra and elemental analysis. All the new compounds were screened for their antibacterial activity against 11 type strains of different species of oral streptococci. Keywords: acylthiosemicarbazide, 2-amino-1,3,4-thiadiazole, 2-amino-1,3,4-oxadiazole, 1,2,4-triazole-3(4H)-thione, oral streptococci

Issue: 2010, Volume 61, Issue 2
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