GdCl3 catalysed Grieco condensation:: A facile approach for the synthesis of novel pyrimidine and annulated pyrimidine fused indazole derivatives in single pot under mild conditions and their anti-microbial activity

被引:44
|
作者
Yakaiah, T. [1 ]
Lingaiah, B. P. V. [1 ]
Narsaiah, B. [1 ]
Kumar, K. Pranay [2 ]
Murthy, U. S. N. [2 ]
机构
[1] Indian Inst Chem Technol, Fluroorgan Div, Hyderabad 500007, Andhra Pradesh, India
[2] Indian Inst Chem Technol, Biol Div Bioinformat, Hyderabad 500007, Andhra Pradesh, India
关键词
regioisomers; indazoles; pyrimidines; cyclisation; olefins; diazadiene;
D O I
10.1016/j.ejmech.2007.03.031
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Indazole regioisomers such as 3-amino-4-(trifluoromethyl)-6-phenyl-1H-indazole-7-carbonitrile 1 and 3-amino-6-(trifluoromethyl)-4-phenyl-1H-indazole-7-carbonitrile 2 were independently reacted with formaldehyde followed by unsymmetrical, symmetrical and cyclic electron rich olefins in presence of GdCl3 as catalyst and obtained pyrimidine fused indazole derivatives 3 and 4, respectively. The reaction is found to be concerted and an exclusive product is formed. Representative examples of compounds 3 and 4 were screened against Gram-positive, Gram-negative bacteria and fungal species such as yeast and filamentous fungi in vitro. Compound 3f showed significant activity against all species of Grain-positive and Gram-negative bacteria, whereas compounds 3h and 4a showed the least activity with reference to penicillin as well as streptomycin. Similarly compound 3c showed promising activity against yeast and filamentous fungi whereas compound 3f is inactive at the rnaximum concentration of 150 mu g/mL. (c) 2007 Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:341 / 347
页数:7
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