echemi logo
Product
  • Product
  • Supplier
  • Inquiry
    Home > Medical News > Medical World News > The Synthetic Routes of 2-Pyrimidinamine, 5-(chloromethyl)-, hydrochloride (1:1)

    The Synthetic Routes of 2-Pyrimidinamine, 5-(chloromethyl)-, hydrochloride (1:1)

    • 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

    The synthesis of 2-pyrimidinamine, 5-(chloromethyl)-, hydrochloride (1:1) is a critical step in the production of various pharmaceuticals, agrochemicals, and other chemical products.
    This compound has a wide range of applications, including as an intermediate in the production of anti-cancer drugs, antifungal agents, and herbicides.


    The synthesis of 2-pyrimidinamine, 5-(chloromethyl)-, hydrochloride (1:1) can be accomplished through several different synthetic routes, each with its own advantages and disadvantages.
    The choice of synthetic route depends on the availability of starting materials, the desired yield and purity of the product, and the cost and complexity of the synthesis.


    One synthetic route to 2-pyrimidinamine, 5-(chloromethyl)-, hydrochloride (1:1) involves the reduction of 2-chloromethyl-5-nitro-1H-pyrimidine to form 2-chloromethyl-1H-pyrimidine, followed by condensation with acetyl sulfide to form 5-(chloromethyl)-2-pyrimidinamine.
    This compound can then be treated with hydrochloric acid to form the hydrochloride salt.


    An alternative synthetic route to 2-pyrimidinamine, 5-(chloromethyl)-, hydrochloride (1:1) involves the reaction of 2-amino-5-chloromethyl-1H-pyrimidine with chloroform to form 2-chloromethyl-5-(2-chlorovinyl)-1H-pyrimidine, followed by reduction with lithium aluminum hydride to form 5-(chloromethyl)-2-pyrimidinamine.
    This compound can then be treated with hydrochloric acid to form the hydrochloride salt.


    A third synthetic route to 2-pyrimidinamine, 5-(chloromethyl)-, hydrochloride (1:1) involves the reaction of 2-chloromethyl-5-nitro-1H-pyrimidine with sarcosine to form 2-chloromethyl-5-nitropyridine-3,4-dicarboxylic acid, followed by hydrolysis to form 5-(chloromethyl)-2-pyrimidinamine.
    This compound can then be treated with hydrochloric acid to form the hydrochloride salt.


    Regardless of the synthetic route chosen, the final product must be purified and characterized to ensure its purity and identity.
    This may involve techniques such as chromatography, spectroscopy, and mass spectrometry.


    In conclusion, the synthesis of 2-pyrimidinamine, 5-(chloromethyl)-, hydrochloride (1:1) is a complex process that can be accomplished through several different synthetic routes.
    The choice of synthetic route will depend on a variety of factors, including the desired yield and purity of the product, the availability of starting materials, and the cost and complexity of the synthesis.
    The final product must be purified and characterized to ensure its purity and identity, and this may involve techniques such as chromatography, spectroscopy, and mass spectrometry.


    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.