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    Home > Active Ingredient News > Antitumor Therapy > The Synthetic Routes of Imatinib (Piperidine)-N-oxide

    The Synthetic Routes of Imatinib (Piperidine)-N-oxide

    • Last Update: 2023-05-01
    • Source: Internet
    • Author: User
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    Imatinib (also known as Glivec) is a medication used to treat certain types of cancer, such as chronic myeloid leukemia and gastrointestinal stromal tumors.
    Its active ingredient is imatinib mesylate, which is a derivative of imatinib.
    Imatinib was first synthesized in 1998 by a team of researchers led by A.
    J.
    Collins at Novartis Research Institute.
    Since then, several synthetic routes have been developed to produce imatinib and its derivatives.


    One of the most popular synthetic routes for imatinib is the synthesis of imatinib-N-oxide, which is a piperidine derivative of imatinib.
    This synthetic route involves the conversion of imatinib to its N-oxide derivative, followed by hydrolysis to yield imatinib-N-oxide.
    The synthesis of imatinib-N-oxide can be accomplished through several different methods, including chemical and biochemical approaches.


    Chemical Synthesis of Imatinib-N-oxide


    One of the most common chemical methods for synthesizing imatinib-N-oxide involves the use of hydrochloric acid and sodium nitrate in the presence of a solvent such as acetonitrile or ethanol.
    The reaction is typically carried out at room temperature and involves the addition of the reagents to a solution of imatinib in the solvent.
    The resulting mixture is then stirred for several hours before being treated with water and extracted with a solvent such as ether or dichloromethane.
    The organic layer is then dried over anhydrous sodium sulfate and concentrated under reduced pressure to yield imatinib-N-oxide.


    Biochemical Synthesis of Imatinib-N-oxide


    Another approach to synthesizing imatinib-N-oxide is through a biochemical route that involves the action of an enzyme called P450.
    This method involves the conversion of imatinib to its N-oxide derivative using the P450 enzyme, which is present in a variety of organisms such as bacteria, fungi, and mammalian cells.
    The P450 enzyme is able to convert imatinib to its N-oxide derivative through the addition of oxygen, which is present in the enzyme.
    The resulting imatinib-N-oxide can then be isolated from the reaction mixture using a variety of methods, such as crystallization or chromatography.


    Applications of Imatinib-N-oxide


    Imatinib-N-oxide has a wide range of applications in the pharmaceutical industry, including the treatment of cancer and autoimmune disorders.
    It has also been shown to have anti-inflammatory and anti-fibrotic properties, making it a promising candidate for the treatment of fibrotic diseases such as pulmonary fibrosis and kidney fibrosis.
    In addition, imatinib-N-oxide has been shown to have chemopreventive effects in animal models of cancer, indicating its potential as a chemopreventive agent in humans.


    Conclusion


    The synthetic routes of imatinib-N-oxide are diverse and vary in complexity and cost.
    The choice of synthetic route depends on the desired yield, purity, and cost of the final product.
    Imatinib-N-oxide has a wide range of applications in the pharmaceutical industry and is an important intermediate in the synthesis of other medicinal compounds.
    Its potential as a chemopreventive agent and anti-fibrotic agent also makes it an important compound for further research and development.
    Overall, the synthesis of imatinib-N-oxide remains an important area of research in the pharmaceutical industry and is expected to continue to be a valuable tool in the development of new treatments for cancer and other diseases.


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