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    Home > Medical News > Medical World News > The Synthetic Routes of 3,6-Di(1H-imidazol-1-yl)pyridazine

    The Synthetic Routes of 3,6-Di(1H-imidazol-1-yl)pyridazine

    • Last Update: 2023-05-16
    • Source: Internet
    • Author: User
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    3,6-Di(1H-imidazol-1-yl)pyridazine is a heterocyclic compound with a unique structure and diverse range of properties.
    It has been widely studied for its potential use in various applications such as pharmaceuticals, agrochemicals, and materials science.
    The synthetic routes for this compound vary, and several methods have been developed to synthesize it.
    In this article, we will discuss some of the most commonly used synthetic routes for 3,6-Di(1H-imidazol-1-yl)pyridazine.


    One of the most common methods for synthesizing 3,6-Di(1H-imidazol-1-yl)pyridazine is through the reaction of 2-chloropyridine with 1H-imidazole in the presence of a catalyst such as sodium hydroxide.
    This reaction results in the formation of the imidate intermediate, which is then reduced to form the desired product.


    Another method for synthesizing 3,6-Di(1H-imidazol-1-yl)pyridazine involves the reaction of 2-aminopyridine with a nitrile in the presence of a strong acid catalyst such as sulfuric acid.
    This reaction results in the formation of the corresponding nitrile, which is then hydrolyzed to form the imidate intermediate.
    The imidate intermediate is then reduced to form the desired product.


    A third method for synthesizing 3,6-Di(1H-imidazol-1-yl)pyridazine involves the reaction of 2-bromopyridine with sodium hydroxide in the presence of a catalyst such as tin(II) chloride.
    This reaction results in the formation of the pyridazine intermediate, which is then converted to the desired product through a series of steps.


    In addition to the above methods, 3,6-Di(1H-imidazol-1-yl)pyridazine can also be synthesized through other methods such as the Suzuki reaction, the Stille reaction, and the Sonogashira reaction.


    One advantage of the synthetic routes for 3,6-Di(1H-imidazol-1-yl)pyridazine is that they can be adapted to large-scale production with relatively ease.
    This makes it a viable option for industrial applications.


    Another advantage of 3,6-Di(1H-imidazol-1-yl)pyridazine is its high thermal stability, which makes it suitable for use in high-temperature applications such as inorganic membranes, electrodes, and catalysts.


    In conclusion, 3,6-Di(1H-imidazol-1-yl)pyridazine is a versatile compound with diverse applications.
    The synthetic routes for this compound are numerous and can be adapted to large-scale production.
    Its high thermal stability makes it suitable for use in high-temperature applications, making it a viable option for industrial applications.


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