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MolBank, volume 2022, issue 2, pages M1386
3,4-Diaminopyridine-2,5-dicarbonitrile
Chmovzh Timofey
1, 2
,
Publication type: Journal Article
Publication date: 2022-06-16
DOI:
10.3390/M1386
Organic Chemistry
Biochemistry
Physical and Theoretical Chemistry
Abstract
Pyridines fused with heterocyclic rings are of great interest as both photovoltaic materials and biologically active compounds. The most convenient precursors for these compounds are pyridine-2,3-diamines. In this communication, 3,4-diaminopyridine-2,5-dicarbonitrile was synthesized by the reaction of 2,5-dibromo-3,4-diaminopyridine with copper cyanide; the best yield of the target compound was achieved by heating the reaction mixture in N,N-dimethylformamide at 120 °C for 6 h. The structure of the newly synthesized compound was established by means of elemental analysis, high resolution mass-spectrometry, 1H, 13C NMR, IR, UV spectroscopy and mass-spectrometry.
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TY - JOUR
DO - 10.3390/M1386
UR - https://doi.org/10.3390%2FM1386
TI - 3,4-Diaminopyridine-2,5-dicarbonitrile
T2 - MolBank
AU - Chmovzh, Timofey
AU - Rakitin, Oleg A.
PY - 2022
DA - 2022/06/16 00:00:00
PB - Multidisciplinary Digital Publishing Institute (MDPI)
SP - M1386
IS - 2
VL - 2022
SN - 1422-8599
ER -
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@article{2022_Chmovzh,
author = {Timofey Chmovzh and Oleg A. Rakitin},
title = {3,4-Diaminopyridine-2,5-dicarbonitrile},
journal = {MolBank},
year = {2022},
volume = {2022},
publisher = {Multidisciplinary Digital Publishing Institute (MDPI)},
month = {jun},
url = {https://doi.org/10.3390%2FM1386},
number = {2},
pages = {M1386},
doi = {10.3390/M1386}
}
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Chmovzh, Timofey, et al. “3,4-Diaminopyridine-2,5-dicarbonitrile.” MolBank, vol. 2022, no. 2, Jun. 2022, p. M1386. https://doi.org/10.3390%2FM1386.
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