Synthesis and antimicrobial activity of new pyridine derivatives-I

被引:67
作者
Patel, Navin B. [1 ]
Agravat, Suresh N. [1 ]
Shaikh, Faiyazalam M. [1 ]
机构
[1] Veer Narmad S Gujarat Univ, Dept Chem, Surat 395007, Gujarat, India
关键词
2-Aminobenzothiazoles; 2-Chloropyridine-3-carboxylic acid; Piperazines; Antimicrobial activity; ANTIBACTERIAL ACTIVITY; POTENT;
D O I
10.1007/s00044-010-9440-0
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
2-Amino substituted benzothiazoles 2a-l and 2-chloropyridine-3-carboxylic acid 3 were used to prepare 2-[N-(substitutedbenzothiazolyl)amino]pyridine-3-carboxylic acids (4a-l) in 2-ethoxy ethanol. Acid chlorides (5a-l) were condensed with 2-hydroxyethyl piperazine (6) and 2,3-dichloropiperazine (7) to prepare amide derivatives 2-[N-(substituted benzothiazolyl)amino]pyridin-3-yl(4-(2-hydroxyethyl)piperazin-1-yl)methanones (8a-l) and 2-[N-(substituted benzothiazolyl) amino]pyridin-3-yl(2,3-dichloropiperazine-1-yl)methanones (9a-l), respectively. The structures of new compounds have been established on the basis of elemental analysis and spectral (IR, H-1 NMR, and Mass spectra) studies. The in vitro antimicrobial activity was screened for all the synthesized compounds. Variable and modest activity were observed against the investigated strains of bacteria and fungi.
引用
收藏
页码:1033 / 1041
页数:9
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