SYNTHESIS AND FUNCTIONALIZATION OF SOME PARA-R-PHENYLIMIDAZO[2,1-B][1,3,4]- THIADIAZOLE DERIVATIVES
DOI:
https://doi.org/10.31618/ESSA.2782-1994.2021.1.68.15Keywords:
2-methyl-6-p-iodophenylimidazo[2,1-b][1,3,4]-thiadiazole, 2-(1-chloro-ethyl)-6-pbromophenylimidazo[2,1-b][1,3,4]-thiadiazole, electrophilic substitution, absorption band, stretching vibrations.Abstract
The article describes the synthesis of new modifications of derivatives of 6-phenyl-, 6-piodophenyl- and 6-p-bromophenylimidazo[2,1-b][1,3,4]-thiadiazoles - N -((6-(4-iodophenyl)-2-R-imidazo[2,1-b][1,3,4]-thiadiazol-5-yl)methyl)-alkyl/ heterylamine based on the Mannich reaction, bromination 2((ethylsulfonyl)methyl)-6-phenylimidazo[2,1-b][1,3,4]-thiadiazole and the structure of the resulting compounds was established on the basis of IR spectroscopy. It was shown that the presence of substituents at the 2-nd position of the thiadiazole fragment and substituents at the 5th and 6th positions of the imidazole fragment of this heterocycle cause the appearance of a nonequivalent absorption band in the imidazo-thiadiazole fragment.
References
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Andanappa K. Gadad, Malleshappa N. Noolvi and Rajshekhar V. Karpoormath. / Synthesis and antitubercular activity of a series of 2- sulfonamido/trifluoromethyl-6-substituted imidazo[2,1-b][1,3,4]thiadiazole derivatives.// Bioorg. Med. Chem. 2004. 12. 5651–5659.
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