Reactions of 1-Amino-5-benzoyl-4-phenyl-1H-pyrimidine-2-one/thione Compounds with Unsymmetrically 1,3-Substituted Diketones
Corresponding Author(s) : ZULBIYE ONAL
zulbiye@erciyes.edu.tr
Asian Journal of Chemistry,
Vol. 20 No. 2 (2008): Vol 20 Issue 2
Abstract
1-Amino-5-benzoyl-4-phenyl-1H-pyrimidine-2-one/thione (1) react with several unsymmetrically 1,3-substituted diketones (2a-f) under different conditions to give the new imine derivatives (3a-f). Unsymmetrically 1,3-substituted diketones derivatives (2a-f) were obtained from 1,5-di-(4-aryl)-4,5-dibromo-1-pentene-3-one and sodium methoxide. All newly synthesized compounds were characterized by elemental analysis, IR and 1H NMR spectral data.
Keywords
1-Amino-5-benzoyl-4-phenyl-1H-pyrimidine-2-one/ thione
Addition reactions
Unsymmetrically 1,3- Substituted diketones
Imines
ONAL, Z. (2010). Reactions of 1-Amino-5-benzoyl-4-phenyl-1H-pyrimidine-2-one/thione Compounds with Unsymmetrically 1,3-Substituted Diketones. Asian Journal of Chemistry, 20(2), 1279–1284. Retrieved from https://asianpubs.org/index.php/ajchem/article/view/12538
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