首页> 外文期刊>Heterocycles: An International Journal for Reviews and Communications in Heterocyclic Chemistry >NEW SCHIFF BASES BASED ON 1-AMINOPYRIMIDIN-2-(1H)-ONE: DESIGN, SYNTHESIS, CHARACTERIZATION AND THEORETICAL CALCULATIONS
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NEW SCHIFF BASES BASED ON 1-AMINOPYRIMIDIN-2-(1H)-ONE: DESIGN, SYNTHESIS, CHARACTERIZATION AND THEORETICAL CALCULATIONS

机译:基于1-氨基嘧啶-2-(1H)的新Schiff碱基:设计,合成,表征和理论计算

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摘要

In this study, 1-amino-5-benzoyl-4-phenylpyrimidin-2(1H)-one (1) was synthesized from 4-benzoyl-5-phenylfuran-2,3-dione and 1-(1-phenylethylidene)semicarbazide in benzene. Since pyrimidine-based Schiff bases have an extensive working range, two new compounds (2, 3) were synthesized from the reaction of this starting material (1) with 3-bromobenzaldehyde or 4-chlorobenzaldehyde. The structures of the synthesized new compounds were clarified employing FT-IR, H-1 NMR, C-13 NMR, and elemental analysis. HOMO, LUMO, and energy gap between them was calculated as theoretical. On the other hand, conformation analysis studies of compounds were carried out for determining the energies of the conformers.
机译:在该研究中,用4-苯甲酰-5-苯基呋喃-2,3-二酮和1-(1-苯基乙烯)氨基脲合成1-氨基-5-苯甲酰-4-苯基吡啶蛋白-2(1H)--ONE(1) 在苯。 由于基于嘧啶的席夫碱具有广泛的工作范围,因此将两个新的化合物(2,3)与该原料(1)的反应合成,其中3-溴苯甲醛或4-氯苯甲醛。 澄清了合成的新化合物的结构,采用FT-IR,H-1 NMR,C-13 NMR和元素分析。 它们之间的同性恋者,Lumo和能量差距计算为理论。 另一方面,进行化合物的构象分析,用于确定塑造剂的能量。

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