Abstract
In this paper we present the synthesis of the new heterocyclic compounds with 5H-dibenzo[a,d][7]annulene moiety obtained by cyclization of 2-acylhydrazinecarbothioamides (2a,b). The acylhydrazinecarbothioamides were obtained by treating 2-(5H-dibenzo[a,d][7]annulen-5-yl)acetohydrazide (1) with 2,5-difluorophenyl or 3-bromophenyl isothiocyanates. 2-Amino-1,3,4-oxadiazoles (3a,b) were synthesized by cyclization of 2-acylhydrazinecarbothioamides in the presence of mercury oxide. The new 1,2,4-triazole-3-thioles (4a,b) were synthesized by cyclization, in alkaline media, of the corresponding acylhydrazinecarbothioamide. The structures of the new compounds synthesized were investigated by 1H-NMR, 13C-NMR, IR and elemental analysis.
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Socea, L. I., Barbuceanu, S. F., Draghici, C., Nitulescu, G. M., Saramet, G., Socea, B., & Apostol, T. V. (2017). New Heterocyclic Compounds from 1,2,4-triazoles and 1,3,4-Oxadiazoles Class Containing 5H-dibenzo[a,d][7]Annulene Moiety. Revista de Chimie, 68(12), 2761–2764. https://doi.org/10.37358/rc.17.12.5972
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