Abstract
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 activity against E. coti ATCC 11229, S. aureus ATCC6538 and C. albicans SATCC 10231.
Original language | English |
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Pages (from-to) | 1273-1275 |
Number of pages | 3 |
Journal | Journal of Heterocyclic Chemistry |
Volume | 37 |
Issue number | 5 |
Publication status | Published - 2000 |
ASJC Scopus subject areas
- Organic Chemistry