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    Home > Medical News > Medical World News > The Synthetic Routes of 7-CHLORO-2,5-DIMETHYL-PYRAZOLO[1,5-A]PYRIMIDINE

    The Synthetic Routes of 7-CHLORO-2,5-DIMETHYL-PYRAZOLO[1,5-A]PYRIMIDINE

    • Last Update: 2023-05-04
    • Source: Internet
    • Author: User
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    7-Chloro-2,5-dimethyl-pyrazolo[1,5-a]pyrimidine is an important intermediate in the synthesis of several pharmaceuticals and agrochemicals.
    This article will discuss the various synthetic routes to this compound in the chemical industry.


    One of the most common methods of synthesizing 7-chloro-2,5-dimethyl-pyrazolo[1,5-a]pyrimidine is through the reaction of 2,5-dimethylpyrazole with chloroacetyl chloride in the presence of a base such as sodium hydroxide.
    This reaction results in the formation of the desired pyrazolo[1,5-a]pyrimidine derivative, which can then be further converted into the desired pharmaceutical or agrochemical product.


    Another synthetic route to 7-chloro-2,5-dimethyl-pyrazolo[1,5-a]pyrimidine involves the reaction of 2,5-dimethylpyrazole with chloroform in the presence of a Lewis acid catalyst such as aluminum chloride.
    This process is known as the Kharasch reaction and results in the formation of the desired pyrazolo[1,5-a]pyrimidine derivative.


    In addition, 7-chloro-2,5-dimethyl-pyrazolo[1,5-a]pyrimidine can also be synthesized through the reaction of 2,5-dimethylpyrazole with chloroacetonitrile in the presence of a base such as triethylamine.
    This reaction is known as the Peterson reaction and results in the formation of the desired pyrazolo[1,5-a]pyrimidine derivative.


    Another route to 7-chloro-2,5-dimethyl-pyrazolo[1,5-a]pyrimidine is through the reaction of 2,5-dimethylpyrazole with chloroform in the presence of a Lewis acid catalyst such as ferric chloride.
    This reaction is known as the Kharasch-Barrow reaction and results in the formation of the desired pyrazolo[1,5-a]pyrimidine derivative.


    In addition, 7-chloro-2,5-dimethyl-pyrazolo[1,5-a]pyrimidine can also be synthesized through the reaction of 2,5-dimethylpyrazole with phosphoryl chloride in the presence of a catalyst such as iodine.
    This reaction is known as the Wolff-Kishner reduction and results in the formation of the desired pyrazolo[1,5-a]pyrimidine derivative.


    Overall, there are several synthetic routes to 7-chloro-2,5-dimethyl-pyrazolo[1,5-a]pyrimidine in the chemical industry.
    These routes involve various reactions such as the Kharasch reaction, Peterson reaction, Kharasch-Barrow reaction, and Wolff-Kishner reduction.
    The choice of synthetic route depends on the specific requirements of the synthesis of the desired pharmaceutical or agrochemical product.


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