STUDIES ON PYRIDONECARBOXYLIC ACIDS AS ANTIBACTERIAL AGENTS——VI. SYNTHESIS AND ANTIBACTERIAL ACTIVITY OF 7-CHLORO-6-FLUORO-1-ETHYT-1, 4-DIHYDRO-4-OXOPYRIDO(2, 3-c)PYRIDAZINE-3-CARBOXYLIC ACID AND DERIVATIVES
1988
The synthesis and in vitro antibacterial activity of 7-chloro-6-fluoro-1-ethyl-1, 4-dihydro-4-oxopyrido (2,3-c) pyridazine-3-carboxylic acid and derivatives were reported. Ethyl 7-chloro-6-fluoro-1,4-dihydro-4-oxopyrido (2,3-c) pyridazine-3-carboxylate Ⅵ was obtained from 2,6-dichloro-5-fluoronicotinitrile Ⅰ through hydrolysis, carboxylic chlorination, condensation with ethyl diazoacetate, reduction of diazo group and cyclization. Compound Ⅵ reacted by different pathways to provide ten free acids which had a minimum inhibitory concentration 100 μg/ml against S. aureus-15, E. coli-1515 and P. aeruginosa-29, while those of compounds Xa and Xb against E. coli-1515 were 50μg/ml.The structures of twenty-four new compounds Ⅳ, Ⅴ, Ⅵ, Ⅶ, Ⅷa~b, Ⅸ a~h and Ⅹa~f, ⅰ~1 were determined by IR; MS; IHNMR and elemental analysis.
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