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    Home > Active Ingredient News > Active Ingredient Products News > The Synthetic Routes of 3-(PIPERIDIN-1-YLSULFONYL)PHENYLBORONIC ACID

    The Synthetic Routes of 3-(PIPERIDIN-1-YLSULFONYL)PHENYLBORONIC ACID

    • Last Update: 2023-05-09
    • Source: Internet
    • Author: User
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    3-(Piperidin-1-ylsulfonyl)phenylboronic acid is an important intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other chemical products.
    The synthesis of this compound has been the subject of extensive research in the chemical industry, with several synthetic routes being developed over the years.


    One of the most commonly used synthetic routes for the preparation of 3-(Piperidin-1-ylsulfonyl)phenylboronic acid involves the reaction of phenylboronic acid with iodomethane in the presence of a bases, such as sodium hydroxide or potassium hydroxide.
    This reaction leads to the formation of the sulfonated derivative of phenylboronic acid, which can then be further transformed into the target compound using various chemical transformations, such as halogenation, nitration, or sulfonation.


    Another synthetic route involves the reaction of phenylboronic acid with 4-iodopyridine in the presence of a catalyst, such as palladium on barium sulfate.
    This reaction leads to the formation of a boronic acid skeleton, which can then be further elaborated into the target compound using various chemical transformations.


    Recently, a more efficient synthetic route for the preparation of 3-(Piperidin-1-ylsulfonyl)phenylboronic acid has been developed, which involves the reaction of phenylboronic acid with piperidine in the presence of a solvent, such as DMF or DMSO.
    This reaction leads to the formation of the sulfonated derivative of phenylboronic acid, which can then be further transformed into the target compound using various chemical transformations, such as halogenation, nitration, or sulfonation.


    Another important synthetic route involves the reaction of phenylboronic acid with 3-iodopropane in the presence of a catalyst, such as iron(III) chloride.
    This reaction leads to the formation of a boronic acid skeleton, which can then be further elaborated into the target compound using various chemical transformations.


    The synthetic routes for 3-(Piperidin-1-ylsulfonyl)phenylboronic acid can vary depending on the desired yield, selectivity, and cost of the final product.
    The choice of synthetic route also depends on the availability of the starting materials and thepurification and isolation methods used.


    In conclusion, the synthetic routes for 3-(Piperidin-1-ylsulfonyl)phenylboronic acid are diverse and can be adapted to suit the specific requirements of the chemical industry.
    The development of more efficient and cost-effective synthetic routes for this important intermediate will continue to be an active area of research in the chemical industry.


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