Experimental and theoretical characterization of organic salt: 2-((4-bromophenyl)amino) pyrido[1,2-a] quinoxalin-11-ium bromide monohydrate synthesized via oxidative cyclization

被引:18
作者
Faizi, Md. Serajul Haque [1 ]
Alam, Mohammad Jane [3 ]
Haque, Ashanul [2 ]
Ahmad, Shabbir [3 ]
Shahid, M. [4 ]
Ahmad, Musheer [5 ]
机构
[1] Jamia Millia Islamia, Dept Chem, New Delhi 110025, India
[2] Sultan Qaboos Univ, Dept Chem, Muscat, Oman
[3] Aligarh Muslim Univ, Dept Phys, Aligarh 202002, Uttar Pradesh, India
[4] Aligarh Muslim Univ, Dept Chem, Aligarh 202002, Uttar Pradesh, India
[5] Aligarh Muslim Univ, Dept Appl Chem, Aligarh 202002, Uttar Pradesh, India
关键词
Oxidative cyclization; Quinoxaline; Pyrido[1,2-a]quinoxaline; Crystal structure; DFT; EFFICIENT SYNTHESIS; IONIC LIQUID; DERIVATIVES; INDEX; WATER; ACID; HOMO; LUMO; GAP;
D O I
10.1016/j.molstruc.2017.12.014
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
Quinoxalines are nitrogen-embedded heterocyclic compounds that possess unique and versatile pharmacological applications. The present article describes synthesis and characterization of organic salt 2-((4-bromophenyl)amino)pyrido [1,2-a]quinoxalin-11-ium bromide (BAPQ), an oxidative cyclized product of N-phenyl-N-(pyridine-2-ylmethylene)benzene-1,4-diamine (PPMD). The structure of the synthesized product was extensively characterized by H-1 NMR, 2D-COSY NMR, MS, IR, UV-vis, X-ray techniques and elemental analysis. The electronic and structural properties of BAPQ was well complemented by performing extensive computational studies (B3LYP/6-311G (d,p) basis sets). Metal-free, mild reaction condition, easy work-up and excellent yield with high purity are main features of this work and thus holds promise for the generation of new compounds of this class. Analytical results indicated ionic nature of the compound with bromide as counterion. DFT calculation showed low kinetic stability and high reactivity of the compound. (C) 2017 Elsevier B.V. All rights reserved.
引用
收藏
页码:457 / 464
页数:8
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