Аннотация:N-(Methoxycarbonyl)trihaloacetimidoylchlorides react with 5-aminopyrazoles under mild conditions to give N-methoxycarbonyl- N’-(5-pyrazolyl)trihaloacetamidines, which furnish 6-trihalomethyl-4H-pyrazolo[3,4-d]pyrimidin-4-ones by thermal intramolecular cyclocondensation.
Тип публикации:
Статья
Язык публикации: английский
Образец цитирования:
M. V. Vovk, A. V. Bol'but, V. I. Boiko, V. V. Pirozhenko, A. N. Chernega, “Synthesis of 1,5-dihydro-3-methyl-6-trihalomethyl-4H-pyrazolo[3,4-d]pyrimidin-4-ones”, Mendeleev Commun., 11:5 (2001), 198–199
Образцы ссылок на эту страницу:
https://www.mathnet.ru/rus/mendc4291
https://www.mathnet.ru/rus/mendc/v11/i5/p198
Эта публикация цитируется в следующих 5 статьяx:
Dmitriy M. Volochnyuk, Oleksandr O. Grygorenko, Alina O. Gorlova, Fluorine in Heterocyclic Chemistry Volume 2, 2014, 291
N. V. Mel'nichenko, V. N. Tkachuk, E. B. Rusanov, V. A. Sukach, V. I. Boiko, M. V. Vovk, “N-Benzyloxycarbonyl-2,2,2-trifluoroacetimidoyl chloride—A convenient reagent for the synthesis of 2-trifluoromethyl-4H-pyrido[1,2-a][1,3,5]triazin-4-one”, Russ J Org Chem, 49:1 (2013), 119
Volodymyr A. Sukach, Viktor M. Tkachuk, Eduard B. Rusanov, Gerd-Volker Röschenthaler, Mykhaylo V. Vovk, “Heterocyclization of N-(1-chloro-2,2,2-trifluoroethylidene)carbamates with β-enaminoesters—a novel synthetic strategy to functionalized trifluoromethylated pyrimidines”, Tetrahedron, 68:40 (2012), 8408
M. O. Lozinskii, A. Y. Il'chenko, “Chemistry of heterocyclic compounds at the Institute of Organic Chemistry, National Academy of Sciences of Ukraine (Review)”, Chem Heterocycl Comp, 45:4 (2009), 376
Mikhail V. Vovk, Andrei V. Bol'but, Vyacheslav I. Boiko, Vladimir V. Pirozhenko, Aleksandr N. Chernega, “ChemInform Abstract: Synthesis of 1,5‐Dihydro‐3‐methyl‐6‐trihalomethyl‐4H‐pyrazolo [3,4‐d]pyrimidin‐4‐ones.”, ChemInform, 33:11 (2002)
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