European Journal of Chemistry

Synthesis and characterization of novel heterocycles based on tetrazine and hydrazonoyl halides



Main Article Content

Abdelwahed Rashad Sayed
Shar Saad Al-Shihry
Mohsen Abdel-Motaal Gomaa

Abstract

The present work describes the preparation and characterization of new pyridazine, thiohydrazonate, bis-pyrazole, bis-triazole and polypyrazoles based on tetrazine and hydrazonoyl halides. The structures of the newly synthesized were elucidated on the basis of their spectral data FT-IR, NMR, Mass and elemental analysis.


icon graph This Abstract was viewed 2685 times | icon graph Article PDF downloaded 913 times

How to Cite
(1)
Sayed, A. R.; Al-Shihry, S. S.; Gomaa, M. A.-M. Synthesis and Characterization of Novel Heterocycles Based on Tetrazine and Hydrazonoyl Halides. Eur. J. Chem. 2014, 5, 267-271.

Article Details

Share
Crossref - Scopus - Google - European PMC
References

[1]. Boulton, J. A.; McKillop, A. In Comprehensive Heterocyclic Chemistry, Pergamon, New York, 1984.

[2]. Sauer, J. In Comprehensive Heterocyclic Chemistry II; Katritzky, A. R.; Rees, C. W.; Scriven, E. F. V. Pergamon Press Oxford, 1996, pp. 901.
http://dx.doi.org/10.1016/B978-008096518-5.00137-4

[3]. Pal, M.; Batchu, V. R.; Khanna, S.; Yeleswarapu K. R. Tetrahedron 2002, 58, 9933-9940.
http://dx.doi.org/10.1016/S0040-4020(02)01352-2

[4]. Tisler, M.; Stanovnik, B. In Heterocyclic Chemistry; Katritzky, A. R., Ed.; Academic: San Diego, 1990, pp. 1.

[5]. Coates, W. J.; McKillop, A. Synthesis 1993, 3, 334-342.
http://dx.doi.org/10.1055/s-1993-25861

[6]. Heinisch, G.; Kopelent, H. In Progress in Medicinal Chemistry, Ellis, G. P., West, G. B., Eds., Elsevier: Amsterdam, 1992, 29, pp. 141-183.

[7]. Ungureanu, M.; Mangalagiu, I.; Grosu, G.; Petrovanu, M. Ann. Pharm. Fr. 1997, 55(2), 69-72.

[8]. Pita, B.; Sotelo, E.; Saurez, M.; Ravina, E.; Ochoa E.; Verdecia, Y.; Novoa, H.; Blaton, N.; de Ranter, C. Peeters O. M., Tetrahedron 2000, 56, 2473-2479.
http://dx.doi.org/10.1016/S0040-4020(00)00082-X

[9]. Campos, M.; Estevez, I.; Ravina, E.; Orallo, F. Gen. Pharmacol. 1998, 30, 201-207.
http://dx.doi.org/10.1016/S0306-3623(97)00108-0

[10]. Sayed, A. R. Tetrahedron 2012, 68(13), 2784-2789.
http://dx.doi.org/10.1016/j.tet.2012.02.011

[11]. Sayed, A. R.; Wiggins, J. S. J. Appl. Poly. Sci. 2011, 120(2), 623-630.
http://dx.doi.org/10.1002/app.33147

[12]. Sayed, A. R. Tetrahedron Lett. 2010, 51, 4490-4493.
http://dx.doi.org/10.1016/j.tetlet.2010.06.060

[13]. Sayed, A. R.; Wiggins, J. S. Polymer 2008, 49(9), 2253-2259.
http://dx.doi.org/10.1016/j.polymer.2008.02.038

[14]. Huisgen, R. Angew. Chem. Int. Ed. Engl. 1963, 10, 565-598.
http://dx.doi.org/10.1002/anie.196305651

[15]. Varvounis, G.; Fiamegos, Y.; Pilidis, G. Adv. Heterocycl. Chem. 2001, 80, 75-165.
http://dx.doi.org/10.1016/S0065-2725(01)80013-1

[16]. Jaroslaw, S. Syn. Comm. 2000, 30(6), 1083-1094.
http://dx.doi.org/10.1080/00397910008087126

[17]. Sayed, A. R.; Youssef, M. M. Eur. J. Med. Chem. in review, 2014.

[18]. Eweiss, N. F.; Osman, A. J. Heterocycl. Chem. 1980, 17, 1713-1717.
http://dx.doi.org/10.1002/jhet.5570170814

[19]. Badawy, M. A.; Abdelhady, S. A.; Ibrahim, Y. A. Liebigs Ann. Chem. 1990, 4, 393-395.
http://dx.doi.org/10.1002/jlac.199019900174

[20]. Sayed, A. R. Tetrahedron 2013, 69, 5293-5298.
http://dx.doi.org/10.1016/j.tet.2013.04.137

[21]. Finnerty, J.; Mitschke, U.; Wentrup, C. J. Org. Chem. 2002, 67, 1084-1092.
http://dx.doi.org/10.1021/jo010398x

[22]. Shawali, A. S.; Farag, A. F.; Albar, H. A.; Dawood, K. M. Tetrahedron 1993, 49, 2761-2766.
http://dx.doi.org/10.1016/S0040-4020(01)86352-3

[23]. Boger, D. L.; Weinreb, S. M. Hetero Diels-Alder Methodology in Organic Synthesis; Academic Press: San Diego, CA, 1987.

[24]. Shawali, A. S.; Hassaneen, H. M. Tetrahedron 1972, 28, 5903-5909.
http://dx.doi.org/10.1016/0040-4020(72)88123-7

[25]. Argyropoulos, N. G.; Mentzafos, D.; Terzis, A. J. Heterocylic Chem. 1990, 27, 1983-1988.
http://dx.doi.org/10.1002/jhet.5570270725

[26]. Argyropoulos, N. G.; Coutouli-Argyrop, E. P. Iakobidis Chim. Chron. New Ser. 1964, 13, 161-165.

[27]. Shawali, A. S.; Sayed, A. R.; Zayed, M. M. J. Sulfur Chem. 2011, 32(4), 311-314.
http://dx.doi.org/10.1080/17415993.2011.586456

Supporting Agencies

Deanship of Scientific Research (Project no, 130178), King Faisal University, Hofuf, 31982, Saudi Arabia
Most read articles by the same author(s)
TrendMD

Dimensions - Altmetric - scite_ - PlumX

Downloads and views

Downloads

Download data is not yet available.

Metrics

Metrics Loading ...
License Terms

License Terms

by-nc

Copyright © 2024 by Authors. This work is published and licensed by Atlanta Publishing House LLC, Atlanta, GA, USA. The full terms of this license are available at https://www.eurjchem.com/index.php/eurjchem/terms and incorporate the Creative Commons Attribution-Non Commercial (CC BY NC) (International, v4.0) License (http://creativecommons.org/licenses/by-nc/4.0). By accessing the work, you hereby accept the Terms. This is an open access article distributed under the terms and conditions of the CC BY NC License, which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited without any further permission from Atlanta Publishing House LLC (European Journal of Chemistry). No use, distribution, or reproduction is permitted which does not comply with these terms. Permissions for commercial use of this work beyond the scope of the License (https://www.eurjchem.com/index.php/eurjchem/terms) are administered by Atlanta Publishing House LLC (European Journal of Chemistry).