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    Home > Active Ingredient News > Drugs Articles > The Instruction of (3R,4R,5S)-ethyl 4-acetamido-5-(diallylamino)-3-(p

    The Instruction of (3R,4R,5S)-ethyl 4-acetamido-5-(diallylamino)-3-(p

    • Last Update: 2023-04-26
    • Source: Internet
    • Author: User
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    The (3R,4R,5S)-ethyl 4-acetamido-5-(diallylamino)-3-(p-tolyl)amino acid is an important intermediate in the chemical industry, used in the production of various chemical compounds, pharmaceuticals, and agrochemicals.
    The synthesis of this compound involves several steps, each of which must be carefully controlled to ensure the desired product is obtained.


    The starting material for the synthesis of (3R,4R,5S)-ethyl 4-acetamido-5-(diallylamino)-3-(p-tolyl)amino acid is (3R,4S)-ethyl 4-acetamido-5-(diallylamino)-3-(p-tolyl)amino acid, which is derived from the reaction of p-toluidine with acrylonitrile in the presence of a strong acid catalyst.
    This intermediate is then reduced using a reducing agent such as lithium aluminum hydride to produce the (3R,4R,5S)-ethyl 4-acetamido-5-(diallylamino)-3-(p-tolyl)amino acid.


    The synthesis of (3R,4R,5S)-ethyl 4-acetamido-5-(diallylamino)-3-(p-tolyl)amino acid is a multi-step process that requires careful control of temperature, reaction time, and the use of protecting groups to ensure the desired product is obtained.
    The first step in the synthesis is the reaction of p-toluidine with acrylonitrile in the presence of a strong acid catalyst, such as sulfuric acid or hydrochloric acid.
    This reaction results in the formation of the (3R,4S)-ethyl 4-acetamido-5-(diallylamino)-3-(p-tolyl)amino acid intermediate.


    The next step in the synthesis of (3R,4R,5S)-ethyl 4-acetamido-5-(diallylamino)-3-(p-tolyl)amino acid is the reduction of the (3R,4S)-ethyl 4-acetamido-5-(diallylamino)-3-(p-tolyl)amino acid intermediate using a reducing agent such as lithium aluminum hydride.
    This reaction involves the removal of the acetamido group and the reduction of the nitrile group to an amide group.


    After the reduction step, the (3R,4R,5S)-ethyl 4-acetamido-5-(diallylamino)-3-(p-tolyl)amino acid is deprotected using a deprotecting agent such as hydrogen chloride, which is used to hydrolyze the tert-butyl and acetamido groups.
    The resulting compound is then purified using a suitable purification method, such as column chromatography or recrystallization, to obtain the desired product.


    (3R,4R,5S)-Ethyl 4-acetamido-5-(diallylamino)-3-(p-tolyl)amino acid is a versatile intermediate that can be used in a variety of chemical reactions to synthesize other chemical compounds, pharmaceuticals, and agrochemicals.
    For example, this compound can be used in the synthesis of antibiotics, anti-inflammatory drugs, and pesticides.
    The biological activity of these compounds depends on the specific chemical structure of the (3R,4R,5S)-ethyl 4-acetamido-5-(diallylamino)-3-(p-tolyl)amino acid and the other chemical compounds that are synthesized from it.


    In conclusion, the synthesis of (3R,4R,5S)-ethyl 4-acetamido-5-(diallylamino)-3-(p-tolyl)amino acid is a complex multi-step process that requires careful control of temperature, reaction time, and the use of protecting groups.
    This compound is an important intermediate in the chemical industry and is used in the synthesis of a variety of chemical compounds, pharmaceuticals, and agrochemicals.
    The biological activity of these compounds depends on the specific chemical structure of the (3R,4R,5



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