Abstract:
New 5,6-dicyanobenzofurans bearing a 2-(thi)oxotetrahydropyrimidine moiety at the 2-position were synthesized from 2-(2-dimethylaminovinyl)-5,6-dicyanobenzofurans, benzaldehydes and (thio)urea in AcOH.
Document Type:
Article
Language: English
Citation:
S. I. Filimonov, Zh. V. Chirkova, I. G. Abramov, S. I. Firgang, G. A. Stashina, K. Yu. Suponitsky, “Synthesis of 2-oxo- and 2-thioxo-5-(benzofuran-2-yl)tetrahydropyrimidines”, Mendeleev Commun., 21:1 (2011), 46–47
Linking options:
https://www.mathnet.ru/eng/mendc2862
https://www.mathnet.ru/eng/mendc/v21/i1/p46
This publication is cited in the following 6 articles:
Mohamed Ould M'hamed, Omar K. Alduaij, “An Efficient One-Pot Synthesis of New 2- Thioxo and 2-oxo-pyrimidine-5-carbonitriles in Ball-Milling Under Solvent-Free and Catalyst-Free Conditions”, Phosphorus, Sulfur, and Silicon and the Related Elements, 189:2 (2014), 235
S. Terentjeva, D. Muceniece, V. Lusis, “Preparation of 6-Unsubstituted 3,4-Dihydropyrimidin-2(1H)-Ones and 2-(Arylamino)Pyrimidines”, Chem Heterocycl Comp, 49:12 (2014), 1757
Zh. V. Chirkova, R. Sh. Tukhvatshin, S. I. Filimonov, S. A. Ivanovskii, I. G. Abramov, S. I. Firgang, G. A. Stashina, K. Yu. Suponitsky, “Synthesis of 7,8-dicyanopyrimido[2,1-b][1,3]benzothiazoles”, Mendeleev Commun., 23:4 (2013), 215–216
Sergey I. Filimonov, Zhanna V. Chirkova, Igor G. Abramov, Sergey I. Firgang, Galina A. Stashina, Yuri A. Strelenko, Dmitriy V. Khakimov, Tatyana S. Pivina, Alexander V. Samet, Kyrill Yu. Suponitsky, “Base-induced transformations of ortho-nitrobenzylketones: intramolecular displacement of nitro group versus nitro-nitrite rearrangement”, Tetrahedron, 68:30 (2012), 5991
Sergei I. Filimonov, Zhanna V. Chirkova, Igor G. Abramov, Sergey I. Firgang, Galina A. Stashina, Kyrill Yu. Suponitsky, “ChemInform Abstract: Synthesis of 2‐Oxo‐ and 2‐Thioxo‐5‐(benzofuran‐2‐yl)tetrahydropyrimidines.”, ChemInform, 42:26 (2011)
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