Unveiling the reaction mechanisms of the synthesis and the excited state intramolecular proton transfer of 2-(2′-hydroxyphenyl)imidazo[1,2-a]pyridine

被引:3
作者
Monreal-Corona, Roger [1 ,2 ]
Stasyuk, Anton J. [1 ,2 ]
Sola, Miquel [1 ,2 ]
Pla-Quintana, Anna [1 ,2 ]
Poater, Albert [1 ,2 ]
机构
[1] Univ Girona, Inst Quim Computac & Catalisi, C Maria Aurelia Capmany 69, Girona 17003, Spain
[2] Univ Girona, Dept Quim, C Maria Aurelia Capmany 69, Girona 17003, Spain
关键词
imidazopyridines; Ortoleva-King reaction; aromaticity; excited state intramolecular proton transfer (ESIPT); ONE-POT SYNTHESIS; GAUSSIAN-BASIS SETS; ELECTRON; AROMATICITY; INDEXES; ESIPT; PSEUDOPOTENTIALS; FLUORESCENCE; DERIVATIVES; 2-AMINOPYRIDINES;
D O I
10.1002/cphc.202400069
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Given its wide variety of applications in the pharmaceutical industry, the synthesis of imidazo[1,2-a]pyridines has been extensively studied since the beginning of the last century. Here, we disclose the mechanism for the synthesis of imidazo[1,2-a]pyridines by means of the Ortoleva-King reaction. We also reveal the reaction pathway leading to the formation of a iodinated byproduct, demonstrating the challenge of preventing the formation of such a byproduct because of the low energy barrier to access it. Moreover, quantum chemistry tools were employed to investigate the mechanism of intramolecular proton transfer in the excited state, and connections with aromaticity were explored.
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页数:6
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