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    Home > Active Ingredient News > Antitumor Therapy > The Synthetic Routes of 2-amino-9-(2-hydroxyethyl)-3H-purin-6-one

    The Synthetic Routes of 2-amino-9-(2-hydroxyethyl)-3H-purin-6-one

    • Last Update: 2023-05-11
    • Source: Internet
    • Author: User
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    The production of 2-amino-9-(2-hydroxyethyl)-3H-purin-6-one, also known as 2-APB, is a complex process that involves several synthetic routes.
    In the chemical industry, the demand for this compound has been on the rise due to its potential use in various applications, including pharmaceuticals and research.
    As such, the development of efficient and cost-effective synthetic routes for 2-APB has become an area of significant interest.


    One of the most widely used synthetic routes for the production of 2-APB involves the condensation of 2-aminopurine with 9-bromo-2-hydroxyethyl-3H-purin-6-one in the presence of a condensing agent such as dicyclohexylcarbodiimide (DCC).
    This reaction results in the formation of a double bond between the two purine rings, which can subsequently be reduced to form the desired product.
    This route has the advantage of providing a high yield of product, but it also involves the use of toxic reagents such as DCC.


    Another synthetic route for the production of 2-APB involves the use of a cycloaddition reaction between an azide and an alkyne.
    This route has the advantage of being more environmentally friendly than the traditional synthetic routes, as it does not involve the use of toxic reagents.
    Additionally, this route can be performed in a single step, resulting in a simple and efficient synthesis process.
    However, the yield of product obtained using this route is lower compared to other synthetic routes.


    A third synthetic route involves the use of a Suzuki-Miyaura coupling reaction between an aryl boronic acid and a phenylboronic acid.
    This route has the advantage of providing a high yield of product and can be easily scaled up for commercial production.
    However, this route requires the use of expensive reagents and specialized equipment.


    In recent years, there has been significant interest in the development of green and sustainable synthetic routes for the production of 2-APB.
    One such route involves the use of aqueous micellar catalysis to perform the synthesis.
    This method uses water as the solvent and surfactants as catalysts, resulting in a more environmentally friendly and cost-effective synthesis process.
    This route has the advantage of providing a high yield of product, and it is also relatively simple and efficient.


    In conclusion, the production of 2-amino-9-(2-hydroxyethyl)-3H-purin-6-one is a complex process that involves several synthetic routes.
    The choice of route depends on several factors, including the yield of product, the cost and availability of reagents, and the environmental impact of the synthesis process.
    As the demand for 2-APB continues to grow, it is likely that new and more efficient synthetic routes will be developed to meet this demand.


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