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    Home > Medical News > Medical World News > The Synthetic Routes of 3-Quinolinecarboxylic acid, 1-ethyl-6-fluoro-1,4-dihydro-4-oxo-7-(1-piperazinyl)-, compd. with 3-pyridinecarboxylic acid (1:1)

    The Synthetic Routes of 3-Quinolinecarboxylic acid, 1-ethyl-6-fluoro-1,4-dihydro-4-oxo-7-(1-piperazinyl)-, compd. with 3-pyridinecarboxylic acid (1:1)

    • Last Update: 2023-05-07
    • Source: Internet
    • Author: User
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    The synthesis of 3-Quinolinecarboxylic acid, 1-ethyl-6-fluoro-1,4-dihydro-4-oxo-7-(1-piperazinyl)-, compd.
    with 3-pyridinecarboxylic acid (1:1) is an important synthetic route in the chemical industry.
    This compound, commonly referred to as a heterocyclic compound, plays a vital role in the production of various chemicals, drugs, and other products.


    The synthesis of 3-Quinolinecarboxylic acid, 1-ethyl-6-fluoro-1,4-dihydro-4-oxo-7-(1-piperazinyl)-, compd.
    with 3-pyridinecarboxylic acid (1:1) can be achieved through various synthetic routes.
    The most common method involves the reaction of 3-Quinolinecarboxylic acid with 1-ethyl-6-fluoro-1,4-dihydro-4-oxo-7-(1-piperazinyl)hydroxylamine, which is then followed by the condensation with 3-pyridinecarboxylic acid.


    The first step in the synthesis of 3-Quinolinecarboxylic acid, 1-ethyl-6-fluoro-1,4-dihydro-4-oxo-7-(1-piperazinyl)-, compd.
    with 3-pyridinecarboxylic acid (1:1) involves the preparation of 3-Quinolinecarboxylic acid.
    This can be achieved through various methods, such as the nitration of quinoline with nitric acid and the subsequent reduction with hydrogen in the presence of a reducing agent, such as palladium on barium sulfate.


    In the next step, 1-ethyl-6-fluoro-1,4-dihydro-4-oxo-7-(1-piperazinyl)hydroxylamine is synthesized through the reaction of 1-ethyl-6-fluoro-1,4-dihydro-4-oxo-7-fluoro-1,4-dihydroquinoline-3-carboxylate, which is prepared by the reaction of 1,4-dihydroquinoline with 6-fluoro-1,4-dihydro-4-oxo-7-fluoro-1,4-dihydroquinoline-3-carboxylic acid, with piperazine in the presence of a strong acid catalyst, such as sulfuric acid.


    Once 1-ethyl-6-fluoro-1,4-dihydro-4-oxo-7-(1-piperazinyl)hydroxylamine is prepared, it can be condensed with 3-Quinolinecarboxylic acid to produce 3-Quinolinecarboxylic acid, 1-ethyl-6-fluoro-1,4-dihydro-4-oxo-7-(1-piperazinyl), compd.
    with 3-pyridinecarboxylic acid (1:1).
    This reaction can be carried out in the presence of a solvent, such as ethyl ether, and a base, such as sodium hydroxide.


    The synthesis of 3-Quinolinecarboxylic acid, 1-ethyl-6-fluoro-1,4-dihydro-4-oxo-7-(1-piperazinyl)-, compd.
    with 3-pyridinecarboxylic acid (1:1) can also be achieved through other synthetic routes, such as the reaction of 3-Quinolinecarboxylic acid with 1-ethyl-6-fluoro-1,4-dihydro-4-oxo-


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