Abstract:
1,3-Dimethyl-4,5-di(ureido)-substituted imidazolidin-2-ones have been synthesised by the nitrosation of 1,3-dimethyl-4,5-di(3-ethylureido)imidazolidin-2-one followed by the reactions of amines with the resulting 1,3-dimethyl-4,5-di(3-nitroso-3-ethylureido)imidazolidin-2-one, and the structure of 1,3-dimethyl-4,5-di(3-ethylureido)imidazolidin-2-one has been confirmed by X-ray diffraction analysis.
Document Type:
Article
Language: English
Citation:
A. N. Kravchenko, E. Yu. Maksareva, S. V. Vasilevskii, O. V. Lebedev, K. A. Lyssenko, “A new approach to the synthesis of 1,3-dimethyl-4,5-disubstituted imidazolidin-2-ones”, Mendeleev Commun., 18:1 (2008), 45–47
Linking options:
https://www.mathnet.ru/eng/mendc3241
https://www.mathnet.ru/eng/mendc/v18/i1/p45
This publication is cited in the following 4 articles:
N. N. Makhova, L. I. Belen'kii, G. A. Gazieva, I. L. Dalinger, L. S. Konstantinova, V. V. Kuznetsov, A. N. Kravchenko, M. M. Krayushkin, O. A. Rakitin, A. M. Starosotnikov, L. L. Fershtat, S. A. Shevelev, V. Z. Shirinian, V. N. Yarovenko, “Progress in the chemistry of nitrogen-, oxygen- and sulfur-containing heterocyclic systems”, Russian Chem. Reviews, 89:1 (2020), 55–124
Mohamed Ali Tabarki, Rafâa Besbes, “Ring expansion of aziridine-2-carboxylates. An efficient entry to imidazolidin-2-ones and oxazolidin-2-imines”, Tetrahedron Letters, 56:14 (2015), 1837
E. V. Ivanov, V. I. Smirnov, V. K. Abrosimov, “Effect of intramolecular cyclization on the enthalpy of dissolution (solvation) of N,N'-dimethylurea in water and methanol at 298.15 K”, Russ Chem Bull, 58:4 (2009), 854
Angelina N. Kravchenko, Elena Yu. Maksareva, Sergei V. Vasilevskii, Oleg V. Lebedev, Konstantin A. Lyssenko, “ChemInform Abstract: A New Approach to the Synthesis of 1,3‐Dimethyl‐4,5‐disubstituted Imidazolidin‐2‐ones (IV).”, ChemInform, 39:28 (2008)
Contact us: