2-Amino-5-chloro-1<i>H</i>-pyrrole-3,4-dicarbonitrile
The reaction of tetracyanoethylene (TCNE) with HCl (g) in the presence of Sn (1 equiv) and AcOH resulted in 2-amino-5-chloro-1<i>H</i>-pyrrole-3,4-dicarbonitrile in a 74% yield. The compound was fully characterized.
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doaj-3765b973ed7d4681800713e61be0e45c2021-02-14T00:03:48ZengMDPI AGMolbank1422-85992021-02-012021M1191M119110.3390/M11912-Amino-5-chloro-1<i>H</i>-pyrrole-3,4-dicarbonitrileAndreas S. Kalogirou0Panayiotis A. Koutentis1Department of Life Sciences, School of Sciences, European University Cyprus, 6 Diogenis Str., Engomi, P. O. Box 22006, 1516 Nicosia, CyprusDepartment of Chemistry, University of Cyprus, P. O. Box 20537, 1678 Nicosia, CyprusThe reaction of tetracyanoethylene (TCNE) with HCl (g) in the presence of Sn (1 equiv) and AcOH resulted in 2-amino-5-chloro-1<i>H</i>-pyrrole-3,4-dicarbonitrile in a 74% yield. The compound was fully characterized.https://www.mdpi.com/1422-8599/2021/1/M1191TCNEheterocyclepolyfunctionalizedpyrrolecyano group |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Andreas S. Kalogirou Panayiotis A. Koutentis |
spellingShingle |
Andreas S. Kalogirou Panayiotis A. Koutentis 2-Amino-5-chloro-1<i>H</i>-pyrrole-3,4-dicarbonitrile Molbank TCNE heterocycle polyfunctionalized pyrrole cyano group |
author_facet |
Andreas S. Kalogirou Panayiotis A. Koutentis |
author_sort |
Andreas S. Kalogirou |
title |
2-Amino-5-chloro-1<i>H</i>-pyrrole-3,4-dicarbonitrile |
title_short |
2-Amino-5-chloro-1<i>H</i>-pyrrole-3,4-dicarbonitrile |
title_full |
2-Amino-5-chloro-1<i>H</i>-pyrrole-3,4-dicarbonitrile |
title_fullStr |
2-Amino-5-chloro-1<i>H</i>-pyrrole-3,4-dicarbonitrile |
title_full_unstemmed |
2-Amino-5-chloro-1<i>H</i>-pyrrole-3,4-dicarbonitrile |
title_sort |
2-amino-5-chloro-1<i>h</i>-pyrrole-3,4-dicarbonitrile |
publisher |
MDPI AG |
series |
Molbank |
issn |
1422-8599 |
publishDate |
2021-02-01 |
description |
The reaction of tetracyanoethylene (TCNE) with HCl (g) in the presence of Sn (1 equiv) and AcOH resulted in 2-amino-5-chloro-1<i>H</i>-pyrrole-3,4-dicarbonitrile in a 74% yield. The compound was fully characterized. |
topic |
TCNE heterocycle polyfunctionalized pyrrole cyano group |
url |
https://www.mdpi.com/1422-8599/2021/1/M1191 |
work_keys_str_mv |
AT andreasskalogirou 2amino5chloro1ihipyrrole34dicarbonitrile AT panayiotisakoutentis 2amino5chloro1ihipyrrole34dicarbonitrile |
_version_ |
1724271203550494720 |