echemi logo
Product
  • Product
  • Supplier
  • Inquiry
    Home > Medical News > Medical World News > The Synthetic Routes of 4,5-Diamino-6-hydroxypyrimidine

    The Synthetic Routes of 4,5-Diamino-6-hydroxypyrimidine

    • Last Update: 2023-05-07
    • Source: Internet
    • Author: User
    Search more information of high quality chemicals, good prices and reliable suppliers, visit www.echemi.com

    4,5-Diamino-6-hydroxypyrimidine is an important chemical compound that finds numerous applications in the pharmaceutical, agrochemical, and other industries.
    The synthesis of 4,5-diamino-6-hydroxypyrimidine involves several steps, and the selection of the appropriate synthetic route depends on various factors such as cost, availability of reagents, and the desired purity of the product.
    In this article, we will discuss some of the commonly used synthetic routes for 4,5-diamino-6-hydroxypyrimidine.


    1. The Mannich reaction
      The Mannich reaction is a commonly used synthetic route for the preparation of 4,5-diamino-6-hydroxypyrimidine.
      In this process, a primary or secondary amine is reacted with formaldehyde and an aldehyde in the presence of a base such as sodium hydroxide.
      The reaction produces a Mannich base, which can be further hydrolyzed to yield 4,5-diamino-6-hydroxypyrimidine.
    2. The Zemanek-Green reaction
      The Zemanek-Green reaction is another commonly used synthetic route for the preparation of 4,5-diamino-6-hydroxypyrimidine.
      In this process, a substituted phenyl isocyanate is reacted with sodium hydroxide in water to yield a phenylamine derivative.
      The phenylamine derivative is then treated with a mineral acid to produce 4,5-diamino-6-hydroxypyrimidine.
    3. The HCl-H2O2 reaction
      The HCl-H2O2 reaction is a simple and cost-effective synthetic route for the preparation of 4,5-diamino-6-hydroxypyrimidine.
      In this process, hydrochloric acid and hydrogen peroxide are reacted in water to produce 4,5-diamino-6-hydroxypyrimidine through a series of steps.
    4. The Kjeldahl-Deeth reaction
      The Kjeldahl-Deeth reaction is a multi-step synthetic route for the preparation of 4,5-diamino-6-hydroxypyrimidine.
      In this process, a benzaldehyde is treated with a mixture of sodium hydroxide and nickel sulfate in the presence of water to produce a benzylamine derivative.
      The benzylamine derivative is then hydrogenated to yield 4,5-diamino-6-hydroxypyrimidine.

    In conclusion, there are several synthetic routes available for the preparation of 4,5-diamino-6-hydroxypyrimidine.
    The selection of the appropriate route depends on the specific requirements of the application and the cost and availability of the reagents.
    The synthetic routes discussed above are commonly used in the chemical industry and have been found to be effective in the production of 4,5-diamino-6-hydroxypyrimidine.


    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.

    Related Articles

    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.