A new series of 1,2,4,8-tetraazaspiro[4.5]dec-2-enes containing 1,2,4-triazole, piperidine and sulfonamide moieties have been synthesized from the reaction of 4-piperidone benzoylhydrazones having 1-methyl, 1-benzyl, and 1-isopropyl groups with appropriate nitrilimines. The microanalysis and spectral data (IR, 1H NMR, 13C NMR and MS) of the synthesized compounds are in full agreement with their molecular structure. The microbial features of the synthesized compounds were studied by a known method. Some of titled compounds exhibited significant antimicrobial activity on several strains of microbes.
Published in | American Journal of Heterocyclic Chemistry (Volume 3, Issue 1) |
DOI | 10.11648/j.ajhc.20170301.11 |
Page(s) | 1-7 |
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Nitrilimines, Piperidine, Sulfonamide, 1,2,4,8-tetraazaspiro[4.5]dec-2-ene
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APA Style
Hany Mahmoud Dalloul, Khaled A. El-nwairy, Ali Zayed Shorafa, Ahmed Sulyman Abu Samaha. (2017). Synthesis and Antimicrobial Activities Evaluation of New Spiro[4.5]dec-2-enes Containing 1,2,4-Triazole, Piperidine and Sulfonamide Moieties. American Journal of Heterocyclic Chemistry, 3(1), 1-7. https://doi.org/10.11648/j.ajhc.20170301.11
ACS Style
Hany Mahmoud Dalloul; Khaled A. El-nwairy; Ali Zayed Shorafa; Ahmed Sulyman Abu Samaha. Synthesis and Antimicrobial Activities Evaluation of New Spiro[4.5]dec-2-enes Containing 1,2,4-Triazole, Piperidine and Sulfonamide Moieties. Am. J. Heterocycl. Chem. 2017, 3(1), 1-7. doi: 10.11648/j.ajhc.20170301.11
AMA Style
Hany Mahmoud Dalloul, Khaled A. El-nwairy, Ali Zayed Shorafa, Ahmed Sulyman Abu Samaha. Synthesis and Antimicrobial Activities Evaluation of New Spiro[4.5]dec-2-enes Containing 1,2,4-Triazole, Piperidine and Sulfonamide Moieties. Am J Heterocycl Chem. 2017;3(1):1-7. doi: 10.11648/j.ajhc.20170301.11
@article{10.11648/j.ajhc.20170301.11, author = {Hany Mahmoud Dalloul and Khaled A. El-nwairy and Ali Zayed Shorafa and Ahmed Sulyman Abu Samaha}, title = {Synthesis and Antimicrobial Activities Evaluation of New Spiro[4.5]dec-2-enes Containing 1,2,4-Triazole, Piperidine and Sulfonamide Moieties}, journal = {American Journal of Heterocyclic Chemistry}, volume = {3}, number = {1}, pages = {1-7}, doi = {10.11648/j.ajhc.20170301.11}, url = {https://doi.org/10.11648/j.ajhc.20170301.11}, eprint = {https://article.sciencepublishinggroup.com/pdf/10.11648.j.ajhc.20170301.11}, abstract = {A new series of 1,2,4,8-tetraazaspiro[4.5]dec-2-enes containing 1,2,4-triazole, piperidine and sulfonamide moieties have been synthesized from the reaction of 4-piperidone benzoylhydrazones having 1-methyl, 1-benzyl, and 1-isopropyl groups with appropriate nitrilimines. The microanalysis and spectral data (IR, 1H NMR, 13C NMR and MS) of the synthesized compounds are in full agreement with their molecular structure. The microbial features of the synthesized compounds were studied by a known method. Some of titled compounds exhibited significant antimicrobial activity on several strains of microbes.}, year = {2017} }
TY - JOUR T1 - Synthesis and Antimicrobial Activities Evaluation of New Spiro[4.5]dec-2-enes Containing 1,2,4-Triazole, Piperidine and Sulfonamide Moieties AU - Hany Mahmoud Dalloul AU - Khaled A. El-nwairy AU - Ali Zayed Shorafa AU - Ahmed Sulyman Abu Samaha Y1 - 2017/03/01 PY - 2017 N1 - https://doi.org/10.11648/j.ajhc.20170301.11 DO - 10.11648/j.ajhc.20170301.11 T2 - American Journal of Heterocyclic Chemistry JF - American Journal of Heterocyclic Chemistry JO - American Journal of Heterocyclic Chemistry SP - 1 EP - 7 PB - Science Publishing Group SN - 2575-5722 UR - https://doi.org/10.11648/j.ajhc.20170301.11 AB - A new series of 1,2,4,8-tetraazaspiro[4.5]dec-2-enes containing 1,2,4-triazole, piperidine and sulfonamide moieties have been synthesized from the reaction of 4-piperidone benzoylhydrazones having 1-methyl, 1-benzyl, and 1-isopropyl groups with appropriate nitrilimines. The microanalysis and spectral data (IR, 1H NMR, 13C NMR and MS) of the synthesized compounds are in full agreement with their molecular structure. The microbial features of the synthesized compounds were studied by a known method. Some of titled compounds exhibited significant antimicrobial activity on several strains of microbes. VL - 3 IS - 1 ER -