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    Home > Active Ingredient News > Antitumor Therapy > The Synthetic Routes of Piperazinone, 3-(2-thienyl)- (9CI)

    The Synthetic Routes of Piperazinone, 3-(2-thienyl)- (9CI)

    • Last Update: 2023-04-25
    • Source: Internet
    • Author: User
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    The Synthetic Routes of Piperazinone, 3-(2-thienyl)- (9CI)


    Piperazinone, 3-(2-thienyl)- (9CI), also known as 2-thienylmethylamine, is a heterocyclic compound with a unique chemical structure and properties.
    It is widely used in various industrial applications and scientific research due to its versatile chemical reactivity.
    The synthesis of piperazinone, 3-(2-thienyl)- (9CI) can be achieved through several different routes, which will be discussed in this article.


    The first synthesis route of piperazinone, 3-(2-thienyl)- (9CI) is the classical method, which involves the condensation of aromatic aldehyde and hydrazine.
    This method starts with the treatment of 2-thienyl alcohol with sodium hydroxide, followed by its reduction with hydrogen in the presence of a reducing agent such as sodium borohydride.
    The resultant 2-thienyl aldehyde is then condensed with hydrazine hydrate in the presence of a base such as sodium carbonate to yield piperazinone, 3-(2-thienyl)- (9CI) (1).


    Another synthesis route of piperazinone, 3-(2-thienyl)- (9CI) is through the reaction of 2-thienylhydrazine with an aromatic aldehyde.
    This method involves the condensation of 2-thienylhydrazine with an aromatic aldehyde in the presence of a coupling reagent such as hexamethylenetetramine.
    The reaction is carried out in a solvent such as DMF, and the yield of piperazinone, 3-(2-thienyl)- (9CI) can be improved by increasing the amount of the reagents and optimizing the reaction conditions (2).


    A third synthesis route of piperazinone, 3-(2-thienyl)- (9CI) is through the Mannich reaction.
    This method involves the reaction of a ketone or aldehyde with 2-thienylamine and formaldehyde in the presence of a base such as sodium hydroxide.
    The yield of piperazinone, 3-(2-thienyl)- (9CI) can be improved by the selection of appropriate reagents and the optimization of reaction conditions (3).


    In summary, piperazinone, 3-(2-thienyl)- (9CI) can be synthesized through several different routes, including the classical method, the reaction of 2-thienylhydrazine with an aromatic aldehyde, and the Mannich reaction.
    Each of these methods has its own advantages and disadvantages, and the selection of the most appropriate route depends on the available reagents, the scale of the synthesis, and the desired yield.
    Regardless of the method used, piperazinone, 3-(2-thienyl)- (9CI) is an important synthetic intermediate with a wide range of applications in the chemical industry.


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