Synthesis of novel 1,5-disubstituted pyrrolo[1,2-a]quinazolines and their evaluation for anti-bacterial and anti-oxidant activities

被引:33
作者
Kazemi, Shaghayegh Sadat [1 ]
Keivanloo, Ali [1 ]
Nasr-Isfahani, Hossein [1 ]
Bamoniri, Abdolhamid [2 ]
机构
[1] Shahrood Univ Technol, Sch Chem, Shahrood 3619995161, Iran
[2] Univ Kashan, Dept Organ Chem, Fac Chem, Kashan, Iran
关键词
CONVENIENT SYNTHESIS; DERIVATIVES; PYRROLE; CYTOTOXICITY; QUINAZOLINONES; INHIBITION; ALKALOIDS; EFFICIENT; THROMBIN; ANALOGS;
D O I
10.1039/c6ra21219k
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A new series of 1,5-disubstituted pyrrolo[1,2-a]quinazoline derivatives were prepared from 2-chloro-4-substituted quinazolines, propargyl alcohol, and secondary amines through novel multi-component reactions. These one-pot reactions, carried out in the presence of a palladium-copper catalyst, provide an efficient method for the synthesis of functionalized pyrrolo[1,2-a]quinazolines in good-to-high yields. A number of synthesized compounds were screened for their in vitro anti-bacterial activity against Gram-positive and Gram-negative bacteria using a well-diffusion method. Also the anti-oxidant activity of the products was evaluated using the DPPH (2,2-diphenyl-2-picrylhydrazyl) assays.
引用
收藏
页码:92663 / 92669
页数:7
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