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2-Amino-5-chloro-1H-pyrrole-3,4-dicarbonitrile
1
Department of Life Sciences, School of Sciences, European University Cyprus, 6 Diogenis Str., Engomi, P. O. Box 22006, 1516 Nicosia, Cyprus
2
Department of Chemistry, University of Cyprus, P. O. Box 20537, 1678 Nicosia, Cyprus
*
Author to whom correspondence should be addressed.
Academic Editor: Luke R. Odell
Molbank 2021, 2021(1), M1191; https://doi.org/10.3390/M1191
Received: 6 February 2021 / Accepted: 11 February 2021 / Published: 13 February 2021
(This article belongs to the Special Issue Heterocycle Reactions)
The reaction of tetracyanoethylene (TCNE) with HCl (g) in the presence of Sn (1 equiv) and AcOH resulted in 2-amino-5-chloro-1H-pyrrole-3,4-dicarbonitrile in a 74% yield. The compound was fully characterized.
Keywords:
TCNE; heterocycle; polyfunctionalized; pyrrole; cyano group
This is an open access article distributed under the Creative Commons Attribution License which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited
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MDPI and ACS Style
Kalogirou, A.S.; Koutentis, P.A. 2-Amino-5-chloro-1H-pyrrole-3,4-dicarbonitrile. Molbank 2021, 2021, M1191. https://doi.org/10.3390/M1191
AMA Style
Kalogirou AS, Koutentis PA. 2-Amino-5-chloro-1H-pyrrole-3,4-dicarbonitrile. Molbank. 2021; 2021(1):M1191. https://doi.org/10.3390/M1191
Chicago/Turabian StyleKalogirou, Andreas S.; Koutentis, Panayiotis A. 2021. "2-Amino-5-chloro-1H-pyrrole-3,4-dicarbonitrile" Molbank 2021, no. 1: M1191. https://doi.org/10.3390/M1191
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