Abstract:
The interaction of 4,6-dichloro-5-nitropyrimidine 1 with 1-phenyl-3-methylpyrazol-5-one led to the 4,6-dipyrazolyl derivatives of 5-nitropyrimidine 2 and dipyrazolylmethane 3; 2-methylindole reacts with 1 to form diindolylmethane 4 and trisindolylmethane 5; 1,3-dimethylbarbituric acid displaces an indolyl residue in diindolylmethane 4 to form diheterylmethane 6.
Document Type:
Article
Language: English
Citation:
Yu. A. Azev, T. Duelcks, E. Lork, D. Gabel, “Unusual reactions of 4,6-dichloro-5-nitropyrimidine with C-nucleophiles”, Mendeleev Commun., 15:5 (2005), 193–196
Linking options:
https://www.mathnet.ru/eng/mendc3743
https://www.mathnet.ru/eng/mendc/v15/i5/p193
This publication is cited in the following 3 articles:
Yu. A. Azev, O. S. Ermakova, M. A. Ezhikova, M. I. Kodess, V. S. Berseneva, I. S. Kovalev, “Transformations of 6,7-difluoroquinoxaline with Indoles: Synthesis of Indole-Substituted 6,7-difluoroquinoxalines and Tris(indol-3-yl)methane Derivatives”, Chem Nat Compd, 53:3 (2017), 519
Yu. A. Azev, B. V. Golomolzin, S. V. Shorshnev, “Reactions of quinazoline and its 4-oxo- and 4-chloro-substituted derivatives with nucleophiles”, Pharm Chem J, 44:12 (2011), 687
Yuri A. Azev, Thomas Duelcks, Enno Lork, Detlef Gabel, “Unusual Reactions of 4,6‐Dichloro‐5‐nitropyrimidine with C‐Nucleophiles.”, ChemInform, 37:3 (2006)
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