Synthesis of novel 2-(4-(2-morpholinoethoxy)phenyl)-N-phenylacetamide analogues and their antimicrobial study
作者:H P JAYADEVAPPA、G NAGENDRAPPA、S UMESH、S CHANDRASHEKAR
DOI:10.1007/s12039-012-0308-3
日期:2012.9
streptomycin, respectively. Some of the synthesized compounds exhibit superior in vitro activity compared to the standard drugs. In an efficient strategy 2-(4-hydroxyphenyl)acetic acid is first condensed with aromatic amines and then with 1-(2-chloroethyl) morpholine hydrochloride to produce bioactive 2-(4-(2-morpholinoethoxy)phenyl)-N-phenylacetamides. The in vitro antimicrobial activity of the compounds against
从羟苯基乙酸合成了新型的潜在的具有生物活性的2-(4-(2-吗啉代乙氧基)苯基)-N-苯基乙酰胺。通过IR,1 H NMR,质谱研究和元素分析对产物进行表征。通过盘琼脂扩散技术筛选化合物的抗微生物活性。与克霉唑和链霉素相比,分别测试了化合物针对各种真菌和细菌菌株的效力。与标准药物相比,某些合成的化合物具有优异的体外活性。 在有效策略中,首先将2-(4-羟苯基)乙酸与芳族胺缩合,然后与1-(2-氯乙基)吗啉盐酸盐缩合,以生产具有生物活性的2-(4-(2-(吗啉代乙氧基)苯基)-N-苯基乙酰胺。在体外针对选定生物体的化合物的抗微生物活性通过纸片扩散技术和IC研究50个测定值。