echemi logo
Product
  • Product
  • Supplier
  • Inquiry
    Home > Medical News > Medical World News > The Synthetic Routes of 4-Amino-6-bromopyrimidine

    The Synthetic Routes of 4-Amino-6-bromopyrimidine

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

    4-Amino-6-bromopyrimidine is an important intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other chemicals.
    The demand for this compound has been increasing in the chemical industry due to its diverse range of applications.
    There are several synthetic routes available for the preparation of 4-amino-6-bromopyrimidine, each with its own advantages and limitations.


    One of the most common methods for the synthesis of 4-amino-6-bromopyrimidine is the "Hofmann-Löffler reaction," which involves the reaction of 6-bromopyrimidine-5-carbaldehyde with ammonia in the presence of an acid catalyst.
    This method is relatively simple, and the reaction can be easily monitored by TLC or HPLC.


    Another popular method for the synthesis of 4-amino-6-bromopyrimidine is the "Strecker reaction," which involves the reaction of 2-chlorobenzaldehyde with sodium cyanide in the presence of a solvent such as DMF or DMSO.
    This method is more complex than the Hofmann-Löffler reaction, and it requires careful handling of the reagents due to the toxicity of sodium cyanide.


    A third synthetic route for 4-amino-6-bromopyrimidine is the "Mesityleninamine-Aldol condensation" which involves the reaction of mesityleninamine with formaldehyde in the presence of a catalyst such as sodium hydroxide, followed by treatment with sodium hydroxide and water.
    This method is more complex than the Hofmann-Löffler or Strecker reactions, and it requires specialized equipment such as a distillation apparatus.


    A recent study has been developed a new and efficient synthetic route to 4-amino-6-bromopyrimidine, which is the "microwave-assisted hydrochloric acid hydrolysis" of 6-bromo-3-methylpyrimidine-4-carbaldehyde.
    This method is less complex and time-consuming than the other methods, and it provides a high yield of the desired product with a short reaction time.


    In conclusion, there are several synthetic routes available for the preparation of 4-amino-6-bromopyrimidine, each with its own advantages and limitations.
    The choice of a particular route depends on various factors such as the availability of reagents, equipment, and the desired yield and purity of the product.
    The microwave-assisted hydrochloric acid hydrolysis method is a promising new route for the synthesis of 4-amino-6-bromopyrimidine, due to its simplicity and high yield.


    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.