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Open AccessShort Note

4,5,6-Trichloropyrimidine-2-carboxamide

1
Department of Life Sciences, School of Sciences, European University Cyprus, 6 Diogenis Str., Engomi, P. O. Box 22006, Nicosia 1516, Cyprus
2
Department of Chemistry, University of Cyprus, P. O. Box 20537, Nicosia 1678, Cyprus
*
Author to whom correspondence should be addressed.
Academic Editor: Nicholas E. Leadbeater
Molbank 2021, 2021(1), M1190; https://doi.org/10.3390/M1190
Received: 21 January 2021 / Revised: 2 February 2021 / Accepted: 4 February 2021 / Published: 9 February 2021
(This article belongs to the Section Organic Synthesis)
Reaction of 4,5,6-trichloropyrimidine-2-carbonitrile (1) with concentrated sulfuric acid at ca. 20 °C gave 4,5,6-trichloropyrimidine-2-carboxamide (5) in 91% yield. The new compound was fully characterized by IR, MALDI-TOF, NMR and elemental analysis. View Full-Text
Keywords: heterocycle; chloro-substituted; pyrimidine; carboxamide heterocycle; chloro-substituted; pyrimidine; carboxamide
MDPI and ACS Style

Kalogirou, A.S.; Koutentis, P.A. 4,5,6-Trichloropyrimidine-2-carboxamide. Molbank 2021, 2021, M1190. https://doi.org/10.3390/M1190

AMA Style

Kalogirou AS, Koutentis PA. 4,5,6-Trichloropyrimidine-2-carboxamide. Molbank. 2021; 2021(1):M1190. https://doi.org/10.3390/M1190

Chicago/Turabian Style

Kalogirou, Andreas S.; Koutentis, Panayiotis A. 2021. "4,5,6-Trichloropyrimidine-2-carboxamide" Molbank 2021, no. 1: M1190. https://doi.org/10.3390/M1190

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