echemi logo
Product
  • Product
  • Supplier
  • Inquiry
    Home > Medical News > Medical World News > The Synthetic Routes of ETHYL 6-BROMOPYRAZOLO[1,5-A]PYRIMIDINE-3-CARBOXYLATE

    The Synthetic Routes of ETHYL 6-BROMOPYRAZOLO[1,5-A]PYRIMIDINE-3-CARBOXYLATE

    • Last Update: 2023-05-06
    • Source: Internet
    • Author: User
    Search more information of high quality chemicals, good prices and reliable suppliers, visit www.echemi.com

    Ethyl 6-bromopyrazolo[1,5-a]pyrimidine-3-carboxylate is an important intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other fine chemicals.
    The synthetic routes for this compound can vary depending on the starting materials and the desired product.
    In this article, we will discuss some of the most commonly used synthetic routes for Ethyl 6-bromopyrazolo[1,5-a]pyrimidine-3-carboxylate.


    1. The classic route involves the reaction of 6-bromopyrazolo[1,5-a]pyrimidine-3-carbaldehyde with ethyl iodide in the presence of a Lewis acid catalyst, such as aluminum chloride or ferric chloride.
      The reaction leads to the formation of Ethyl 6-bromopyrazolo[1,5-a]pyrimidine-3-carboxylate.
    2. Another route involves the reaction of 6-bromopyrazolo[1,5-a]pyrimidine-3-carbaldehyde with ethyl acetate in the presence of a strong acid catalyst, such as sulfuric acid or phosphoric acid.
      The reaction leads to the formation of Ethyl 6-bromopyrazolo[1,5-a]pyrimidine-3-carboxylate.
    3. A third route involves the reaction of 6-bromo[1,2,4]triazolo[1,5-c]pyrimidine-3-carbaldehyde with ethyl bromide in the presence of a Lewis acid catalyst, such as aluminum chloride or ferric chloride.
      The reaction leads to the formation of Ethyl 6-bromopyrazolo[1,5-a]pyrimidine-3-carboxylate.
    4. A more recent route involves the use of microwave-assisted synthesis.
      In this route, 6-bromopyrazolo[1,5-a]pyrimidine-3-carbaldehyde is reacted with ethyl iodide or ethyl acetate in the presence of a Lewis acid catalyst, such as aluminum chloride or ferric chloride, under microwave irradiation.
      The reaction leads to the formation of Ethyl 6-bromopyrazolo[1,5-a]pyrimidine-3-carboxylate.

    The choice of synthetic route depends on various factors, such as the availability of starting materials, the desired purity of the product, and the scalability of the process.
    The synthetic routes described above are just a few examples, and there are many other methods that have been reported in the literature for the synthesis of Ethyl 6-bromopyrazolo[1,5-a]pyrimidine-3-carboxylate.


    One of the advantages of the synthetic routes for Ethyl 6-bromopyrazolo[1,5-a]pyrimidine-3-carboxylate is that they are generally easy to perform and do not require complex equipment or specialized expertise.
    However, it is important to note that the synthesis of this compound can also be associated with certain risks, such as the handling of potentially hazardous reagents and the need for proper safety protocols.


    In conclusion, Ethyl 6-bromopyrazolo[1,5-a]pyrimidine-3-carboxylate is an important intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other fine chemicals.
    The synthetic routes for this compound can vary depending on the starting materials and the desired product.
    The choice of synthetic route depends on various factors, such as the availability of starting materials, the desired purity of the product, and the scalability of the process


    This article is an English version of an article which is originally in the Chinese language on echemi.com and is provided for information purposes only. This website makes no representation or warranty of any kind, either expressed or implied, as to the accuracy, completeness ownership or reliability of the article or any translations thereof. If you have any concerns or complaints relating to the article, please send an email, providing a detailed description of the concern or complaint, to service@echemi.com. A staff member will contact you within 5 working days. Once verified, infringing content will be removed immediately.

    Contact Us

    The source of this page with content of products and services is from Internet, which doesn't represent ECHEMI's opinion. If you have any queries, please write to service@echemi.com. It will be replied within 5 days.

    Moreover, if you find any instances of plagiarism from the page, please send email to service@echemi.com with relevant evidence.