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    Home > Active Ingredient News > Active Ingredient Products News > The Synthetic Routes of 1-(4-BROMOPHENYLSULFONYL)AZETIDINE

    The Synthetic Routes of 1-(4-BROMOPHENYLSULFONYL)AZETIDINE

    • Last Update: 2023-05-13
    • Source: Internet
    • Author: User
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    1-(4-BROMOPHENYLSULFONYL)AZETIDINE is a pharmaceutical compound that is used in the treatment of hypertension and other cardiovascular conditions.
    The compound is synthesized through several steps, and the selection of the synthetic route depends on the availability of starting materials, the desired yield, and the cost of the synthesis.
    This article provides an overview of the synthetic routes of 1-(4-BROMOPHENYLSULFONYL)AZETIDINE.


    One of the most commonly used synthetic routes for 1-(4-BROMOPHENYLSULFONYL)AZETIDINE involves the reaction of 4-bromophenyl sulfonate with azetidine in the presence of a base such as sodium hydroxide.
    The reaction between the two compounds leads to the formation of the desired product, which can then be isolated and purified using standard chromatography techniques.


    Another synthetic route involves the reaction of 4-bromophenol with sodium hydride in the presence of a polar solvent such as DMF.
    The reaction leads to the formation of 4-bromophenyl sulfonate, which can then be treated with azetidine in the presence of a base such as triethylamine to yield 1-(4-BROMOPHENYLSULFONYL)AZETIDINE.


    In recent years, researchers have focused on developing more efficient and cost-effective synthetic routes for 1-(4-BROMOPHENYLSULFONYL)AZETIDINE.
    One such route involves the use of a palladium catalyst in the Suzuki-Miyaura coupling reaction between 4-bromophenylboronic acid and phenylboronic acid in the presence of a base such as sodium hydroxide.
    The reaction leads to the formation of the desired product, which can be isolated and purified using standard chromatography techniques.


    Another synthetic route involves the use of a lithium amide in the Luche reaction between 4-bromophenyl sulfide and azetidine in the presence of a polar solvent such as DMF.
    The reaction leads to the formation of 1-(4-BROMOPHENYLSULFONYL)AZETIDINE, which can then be isolated and purified using standard chromatography techniques.


    In conclusion, 1-(4-BROMOPHENYLSULFONYL)AZETIDINE is a pharmaceutical compound that is widely used in the treatment of cardiovascular conditions.
    The synthesis of the compound can be achieved through several synthetic routes, each with its advantages and disadvantages.
    Researchers continue to develop more efficient and cost-effective synthetic routes for the production of the compound, with a view to improving the overall process for its manufacture.


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