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    Home > Medical News > Medical World News > The Synthetic Routes of 3-(MethylaMino)pyridazine-4-carbonitrile

    The Synthetic Routes of 3-(MethylaMino)pyridazine-4-carbonitrile

    • Last Update: 2023-05-17
    • Source: Internet
    • Author: User
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    3-(MethylaMino)pyridazine-4-carbonitrile, also known as MMQ, is an important intermediate chemical used in the production of various pharmaceuticals, dyes, and other chemical products.
    The synthesis of MMQ can be achieved through several methods, and the following is a discussion of some of the most commonly used synthetic routes.


    One of the most popular methods for the synthesis of MMQ is the Amadori coupling reaction.
    This reaction involves the reaction of 3-methylaniline with malonic acid in the presence of a Lewis acid catalyst, such as AlCl3, to form MMQ.
    The reaction proceeds through the formation of an enolate intermediate, which then undergoes an intramolecular electrophilic substitution to form the final product.


    Another common synthetic route for MMQ is the reaction of 3-methylaniline with 4-chloropyridine in the presence of a urea-forming catalyst, such as NH4Cl.
    The reaction proceeds through the formation of an isocyanate intermediate, which then reacts with 3-methylaniline to form MMQ.


    A third synthetic route for MMQ involves the reaction of 2,5-dimethylpyrrole with malonic acid in the presence of a Lewis acid catalyst, such as AlCl3, to form the intermediate 2,5-dimethylpyrrole-coumarinylidenemalononitrile.
    The intermediate is then reduced to form MMQ.


    In addition to the above-mentioned methods, there are several other synthetic routes for MMQ, including the use of microwave irradiation, hydrogenation of the pyridazine-4-carbonitrile derivative, and the reaction of 3-methylaniline with 4-nitrophenyl chloride in the presence of a Lewis acid catalyst.


    The choice of synthetic route for MMQ depends on several factors, including the available starting materials, the desired yield and purity of the product, and the cost and availability of the necessary reagents and equipment.
    In general, the Amadori coupling reaction and the reaction of 3-methylaniline with 4-chloropyridine are two of the most commonly used methods for the synthesis of MMQ, due to their relatively high yield and simplicity of operation.


    Once synthesized, MMQ can be further transformed into various pharmaceuticals, dyes, and other chemical products through a variety of chemical reactions, such as nitration, sulfonation, and halogenation.
    MMQ is also commonly used as an intermediate in the synthesis of other chemicals, such as the anti-HIV drug lopinavir and the anti-cancer drug irinotecan.


    Overall, the synthetic routes for 3-(MethylaMino)pyridazine-4-carbonitrile are numerous and varied, and the choice of synthetic route depends on several factors.
    Regardless of the route chosen, the synthesis of MMQ is an important step in the production of various chemical products and pharmaceuticals, and is an area of active research and development in the chemical industry.


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