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

    The Synthetic Routes of 6-broMopyriMidin-4-aMine

    • 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

    Introduction:


    6-broMopyriMidin-4-aMine is an important intermediate in the synthesis of various pharmaceuticals and agrochemicals.
    It is a versatile molecule that can be used in a variety of chemical reactions to form different compounds.
    The synthesis of 6-broMopyriMidin-4-aMine can be achieved through several routes, and the choice of route depends on the availability of starting materials, the desired yield, and the cost of the reaction.
    In this article, we will discuss some of the synthetic routes to 6-broMopyriMidin-4-aMine.


    Route 1: via N-Formylation


    One of the commonly used routes to synthesize 6-broMopyriMidin-4-aMine is via N-formylation of quinoline-2-carboxylic acid.
    The reaction can be carried out in the presence of a strong acid catalyst, such as sulfuric acid or phosphoric acid.
    The reaction is exothermic, and the temperature should be carefully controlled to avoid unwanted side reactions.
    The product can be isolated by precipitation with a polar solvent, such as ethanol, and then recrystallization to obtain pure 6-broMopyriMidin-4-aMine.


    Route 2: via Hydrazoin Reaction


    6-broMopyriMidin-4-aMine can also be synthesized via the hydrazoin reaction of quinoline-2-carboxylic acid with hydrazoic acid.
    The reaction is highly exothermic and should be carried out with caution.
    The product can be isolated by precipitation with a polar solvent, such as ethanol, and then recrystallization to obtain pure 6-broMopyriMidin-4-aMine.


    Route 3: via N-Chlorination


    6-broMopyriMidin-4-aMine can also be synthesized via N-chlorination of quinoline-2-carboxylic acid.
    The reaction can be carried out in the presence of a Lewis acid catalyst, such as aluminum chloride or ferric chloride.
    The product can be isolated by chromatography on a silica gel column using a polar eluent, such as acetonitrile or methanol.


    Conclusion:


    In conclusion, 6-broMopyriMidin-4-aMine can be synthesized via several routes, and the choice of route depends on the availability of starting materials, the desired yield, and the cost of the reaction.
    The synthetic routes described above are commonly used in the chemical industry, and the synthesis of 6-broMopyriMidin-4-aMine is an important step in the synthesis of various pharmaceuticals and agrochemicals.
    The chemical industry is constantly evolving, and new routes to the synthesis of 6-broMopyriMidin-4-aMine will continue to be developed to meet the increasing demand for this important intermediate.


    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.