Central Research Lab, Department of Chemistry, Gulbarga University, Gulbarga 585 106, Karnataka, India.
Eur J Med Chem. 2011 Dec;46(12):6112-8. doi: 10.1016/j.ejmech.2011.10.004. Epub 2011 Oct 8.
A rapid, efficient and environmental benign methodology for the preparation of 2,5-disubstituted indole analogues is developed. 2,5-Disubstituted indole-3-carboxaldehydes (1a-c) undergo Knoevenagel condensation with barbiturates (2 &4), thiazolidine-2,4-dione (6) and 3-methyl-1H-pyrazol-5(4H)-one (8) in solvent-free, NH(4)OAc catalyzed, microwave assisted reaction. Structures of the products thus obtained were confirmed by their m.p, Elemental analysis, IR, (1)H NMR, (13)C NMR and Mass spectral data. The in vitro antioxidant and cytotoxic activities against three tumor cell lines were evaluated and discussed in terms of their structural differences. Among the screened compounds 9b, 9c, 7b and 5b exhibited excellent antioxidant activity. Compounds 9b, 9c and 7b have shown strong cytotoxicity among the compounds tested.
开发了一种快速、高效且环境友好的方法来制备 2,5-取代吲哚类似物。2,5-取代吲哚-3-甲醛(1a-c)在无溶剂、NH(4)OAc 催化、微波辅助反应条件下,与巴比妥酸盐(2 和 4)、噻唑烷-2,4-二酮(6)和 3-甲基-1H-吡唑-5(4H)-酮(8)发生 Knoevenagel 缩合反应。通过熔点、元素分析、IR、(1)H NMR、(13)C NMR 和质谱数据确认了所得产物的结构。根据结构差异,评估并讨论了它们对三种肿瘤细胞系的体外抗氧化和细胞毒性活性。在所筛选的化合物中,9b、9c、7b 和 5b 表现出优异的抗氧化活性。在测试的化合物中,9b、9c 和 7b 表现出很强的细胞毒性。