Synthesis and properties of some 2,3-disubstituted 6-fluoro-7-(4-methyl-1-piperazinyl)quinoxalines
作者:Raid J. Abdel-Jalil、Raed A. Al-Qawasmeh、Wolfgang Voelter、Peter Heeg、Mustafa M. El-Abadelah、Salim S. Sabri
DOI:10.1002/jhet.5570370541
日期:2000.9
The 2,3-disubstituted 6-fluoro-7-(4-methyl-1-piperazinyl)-quinoxalines (3–11) were synthesized for bioassay via reaction of 1.2-diamino-4-fluoro-5-(4-methyl-1-piperazinyl)benzene (2) with the appropriate 1,2-dicarbonyl compounds. However, none of the tested compounds 3–11 showed significant in vitro activ ity against E. coli ATCC11229, S. aureus ATCC6538 and C.albicans SATCC10231.
2,3-二取代的6-氟-7-(4-甲基-1-哌嗪基)-喹喔啉(3-11)通过1.2-二氨基-4-氟-5-(4-甲基- 1-哌嗪基)苯(2)与适当的1,2-二羰基化合物。但是,测试的化合物3-11均未显示出针对大肠杆菌ATCC11229,金黄色葡萄球菌ATCC6538和白色念珠菌SATCC10231的显着体外活性。