synthesis of [(4-chloro-5h-1,2,3-dithiazol-5-ylidene)amino]azines合成[(4-chloro-5h-1 2 3-dithiazol-5-ylidene)氨基]吖嗪.pdfVIP
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synthesis of [(4-chloro-5h-1,2,3-dithiazol-5-ylidene)amino]azines合成[(4-chloro-5h-1 2 3-dithiazol-5-ylidene)氨基]吖嗪
Molecules 2011, 16, 8992-9002; doi:10.3390/molecule
OPEN ACCESS
molecules
ISSN 1420-3049
/journal/molecules
Article
Synthesis of [(4-Chloro-5H-1,2,3-dithiazol-5-ylidene)amino]azines
Panayiotis A. Koutentis *, Maria Koyioni and Sophia S. Michaelidou
Department of Chemistry, University of Cyprus, P.O. Box 20537, 1678 Nicosia, Cyprus;
E-Mails: maria_koyioni@ (M.K.), sophie_michaelidou@ (S.S.M.)
* Author to whom correspondence should be addressed; E-Mail: koutenti@ucy.ac.cy;
Tel.: +357-22-892783; Fax: +357-22-892809.
Received: 26 September 2011; in revised form: 21 October 2011 / Accepted: 21 October 2011 /
Published: 25 October 2011
Abstract: The reactions of 2-, 3- and 4-aminopyridines with 4,5-dichloro-1,2,3-dithiazol-
ium chloride (Appel salt) 4 to give N-(4-chloro-5H-1,2,3-dithiazol-5-ylidene)pyridin-X-
amines 1a (X = 2), 1g (X = 3) and 1k (X = 4) were optimized with respect to base,
temperature and reaction time. Based on these conditions a total of thirteen [(dithiazol-
ylidene)amino]azines 1a-m were prepared and fully characterized.
Keywords: heterocycle; Appel salt; 1,2,3-dithiazoles; condensation; azine
1. Introduction
Select N-(4-chloro-5H-1,2,3-dithiazol-5-ylidene)anilines (N-aryl-1,2,3-dithiazol-5H-imines) show
interesting antitumor [1], antibacterial [2-4], antifungal [5-7], and herbicidal [8] activity. The biological
activity could be due to the 1,2,3-dithiazole ring, that acts as an
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