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    Home > Active Ingredient News > Drugs Articles > The Synthetic Routes of Ravuconazole

    The Synthetic Routes of Ravuconazole

    • Last Update: 2023-05-11
    • Source: Internet
    • Author: User
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    Ravuconazole is an antifungal drug that is widely used to treat a variety of fungal infections, including aspergillosis, blastomycosis, and cryptococcal infections.
    It is synthesized through a series of chemical reactions that convert simple starting materials into the final product.


    The synthesis of ravuconazole involves several steps, including the preparation of the starting materials, the assembly of the chemical framework, and the modification of the molecule to enhance its activity and stability.
    The synthesis of ravuconazole can be divided into three main stages: the preparation of the starting materials, the assembly of the chemical framework, and the modification of the molecule.


    The first stage in the synthesis of ravuconazole is the preparation of the starting materials.
    This involves the synthesis of several different compounds, including the sulfur-containing compound 2,2'-dithiobis(benzothiazole), which is a key intermediate in the synthesis of ravuconazole.
    This compound is prepared through a multi-step synthesis that involves the synthesis of several intermediate compounds.


    The second stage in the synthesis of ravuconazole is the assembly of the chemical framework.
    This involves the synthesis of the benzoxazepine ring system, which is a key component of the ravuconazole molecule.
    This is achieved through a combination of chemical reactions, including the condensation of anthranilic acid with 2-nitrobenzaldehyde, followed by the cyclocondensation of the resulting nitro compound with salicylaldehyde.


    The final stage in the synthesis of ravuconazole is the modification of the molecule to enhance its activity and stability.
    This involves the addition of several functional groups to the molecule, including the introduction of a sulfur-containing group through a process called sulfuration.
    This is achieved through a reaction with elemental sulfur in the presence of a catalyst, such as tetrakis(hydroxymethyl)phosphonium chloride.


    The synthesis of ravuconazole is a complex process that involves several chemical reactions and the synthesis of several intermediate compounds.
    However, it is important to note that the exact details of the synthesis can vary depending on the manufacturer and the specific production process.


    In conclusion, the synthesis of ravuconazole is a multi-step process that involves the preparation of starting materials, the assembly of the chemical framework, and the modification of the molecule to enhance its activity and stability.
    The synthesis of ravuconazole is a crucial step in the production of this important antifungal drug, and it requires a high degree of expertise and specialized equipment.


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