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    Home > Medical News > Medical World News > The Synthetic Routes of ethyl4-amino-2-methylquinoline-6-carboxylate

    The Synthetic Routes of ethyl4-amino-2-methylquinoline-6-carboxylate

    • Last Update: 2023-05-18
    • Source: Internet
    • Author: User
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    Ethyl 4-amino-2-methylquinoline-6-carboxylate, also known as EAMQ, is a compound that is widely used in the fields of pharmaceuticals and agrochemicals.
    It is an important intermediate in the synthesis of various drugs and pesticides, and is also used in research and development of new drugs and chemicals.
    The synthetic routes of EAMQ can vary depending on the starting materials and the desired product, but there are several common methods that are widely used in the chemical industry.


    One of the most common methods for the synthesis of EAMQ is through the use of a reaction called the "Schweizer reaction.
    " This reaction involves the condensation of a substituted aniline with an acyl chloride in the presence of an acid catalyst, such as hydrochloric acid or sulfuric acid.
    The aniline is first treated with a base, such as sodium hydroxide, to convert it to the corresponding sodium salt.
    This salt is then mixed with the acyl chloride and the acid catalyst, and the reaction is carried out at a temperature of around 100-150°C.
    The product of the reaction is a mixture of the desired EAMQ and a similarly substituted compound, which can be separated from the mixture through crystallization or other methods.


    Another common synthetic route for EAMQ is through the use of a reaction called the "Skraup reaction.
    " This reaction involves the reaction of a substituted benzaldehyde with a substituted aniline in the presence of a mineral acid catalyst, such as sulfuric acid or phosphoric acid.
    The reaction is carried out at a temperature of around 100-150°C, and the product of the reaction is a mixture of the desired EAMQ and a similarly substituted compound, which can be separated from the mixture through crystallization or other methods.


    Yet another common synthetic route for EAMQ is through the use of a reaction called the "Koch reaction.
    " This reaction involves the condensation of an aromatic aldehyde with an aromatic amine in the presence of an acid catalyst, such as sulfuric acid or phosphoric acid.
    The reaction is carried out at a temperature of around 100-150°C, and the product of the reaction is a mixture of the desired EAMQ and a similarly substituted compound, which can be separated from the mixture through crystallization or other methods.


    In addition to the above-mentioned reactions, there are also other methods for the synthesis of EAMQ, such as the use of a reaction called the "Grignard reaction," which involves the reaction of an alkyl halide with an amine in the presence of a metal catalyst, such as magnesium or zinc.


    Once the desired EAMQ has been synthesized, it can be purified and isolated through a variety of methods, such as crystallization, distillation, or chromatography.
    The purity of the synthesized EAMQ can be determined through the use of techniques such as spectroscopy, or through the use of chemical tests such as titration.


    In conclusion, the synthetic routes of EAMQ are varied and can depend on the starting materials and the desired product.
    Some of the most common methods for the synthesis of EAMQ include the use of the Schweizer reaction, the Skraup reaction, and the Koch reaction.
    The purity of the synthesized EAMQ can be determined through various methods, and the isolated compound can be used as an intermediate in the synthesis of various drugs and pesticides, or in research and development of new drugs and chemicals.


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