Conventional and microwave-assisted synthesis of quinolone carboxylic acid derivatives


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Abstract

Various antibacterial fluoroquinolone compounds are synthesized by the direct amination of 7-halo-6-fluoroquinolone-3-carboxylic acids with a variety of piperazine derivatives and (4aR,7aR)-octahydro-1H-pyrrolo[3,4-b]pyridine using microwave under different reaction conditions. Solvent free high yield microwave synthesis of antibacterial fluoroquinolone compounds is convenient, rapid and environmentally friendly method.

About the authors

Y. Mirzaie

Department of Chemistry

Author for correspondence.
Email: msc.mirzaee@gmail.com
Iran, Islamic Republic of, Tehran

J. Lari

Department of Chemistry

Email: msc.mirzaee@gmail.com
Iran, Islamic Republic of, Tehran

H. Vahedi

Department of Chemistry

Email: msc.mirzaee@gmail.com
Iran, Islamic Republic of, Tehran

M. Hakimi

Department of Chemistry

Email: msc.mirzaee@gmail.com
Iran, Islamic Republic of, Tehran


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