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Ethyl 5-methyl-7-(4-morpholinophenyl)-4,7-dihydrotetrazolo[1,5-a]pyrimidine-6-carboxylate
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Department of Chemistry, Faculty of Science and Technology, Airlangga University, Surabaya 60115, Indonesia
Author to whom correspondence should be addressed.
Molbank 2018, 2018(3), M1013;
Received: 2 August 2018 / Revised: 19 August 2018 / Accepted: 20 August 2018 / Published: 23 August 2018
(This article belongs to the Special Issue Molecules from Catalytic Processes)
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The title compound was prepared by a two-step reaction. The first step was the formation of a chalcone derivative using Claisen–Schmidt condensation, which was followed by the Michael addition of the formed chalcone with 1,3-dimethylbarbituric acid. The structure of the prepared compound was established by spectral data: FTIR, HRESIMS, 1H- and 13C-NMR. View Full-Text
Keywords: chalcone derivative; 1,3-dimethylbarbituric acid; Michael addition chalcone derivative; 1,3-dimethylbarbituric acid; Michael addition
This is an open access article distributed under the Creative Commons Attribution License which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited (CC BY 4.0).

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Suwito, H.; Sari, R.H.P.; Ul Haq, K.; Kristanti, A.N. 5-[3-(4-Bromophenyl)-1-(2,5-dimethoxyphenyl)-3-oxopropyl]-1,3-dimethylpyrimidine-2,4,6(1H,3H,5H)-tri-one. Molbank 2018, 2018, M1013.

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