echemi logo
Product
  • Product
  • Supplier
  • Inquiry
    Home > Medical News > Medical World News > The Synthetic Routes of 2-Chlorothieno[3,2-d]pyrimidine

    The Synthetic Routes of 2-Chlorothieno[3,2-d]pyrimidine

    • 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

    The synthesis of 2-chlorothieno[3,2-d]pyrimidine, a compound with potential use in the pharmaceutical industry, has been the subject of much research in the chemical industry.
    Synthetic routes to this compound can be broadly classified into two categories: classical synthesis and modern synthesis.


    Classical synthesis involves the use of traditional methods and reagents to synthesize a compound.
    This approach often requires a large number of steps and can be time-consuming and costly.
    In the case of 2-chlorothieno[3,2-d]pyrimidine, classical synthesis methods involve the use of toxic and expensive reagents such as chlorine gas and hydriodic acid.


    Modern synthesis, on the other hand, involves the use of newer techniques and reagents to simplify the synthesis of a compound.
    This approach often requires fewer steps and can be more efficient and cost-effective.
    In the case of 2-chlorothieno[3,2-d]pyrimidine, modern synthesis methods involve the use of less toxic and expensive reagents such as thiourea and hydroxybromide.


    One of the most popular modern synthesis methods for the synthesis of 2-chlorothieno[3,2-d]pyrimidine is the Nathan-Davis oxidation.
    This method involves the use of hydroxybromide and sodium periodate in the presence of water and a polar protic solvent such as ethanol or methanol.
    This method provides the desired product in good yield and is considered to be a more efficient and cost-effective alternative to classical synthesis methods.


    Another modern synthesis method for the synthesis of 2-chlorothieno[3,2-d]pyrimidine is the Mao-Suzuki reaction.
    This method involves the use of thiourea and a palladium catalyst in the presence of a base such as sodium hydroxide.
    This method also provides the desired product in good yield and is considered to be a more efficient and cost-effective alternative to classical synthesis methods.


    In conclusion, the synthetic routes to 2-chlorothieno[3,2-d]pyrimidine have been extensively studied in the chemical industry.
    Classical synthesis methods involve the use of traditional methods and reagents and can be time-consuming and costly.
    Modern synthesis methods, on the other hand, involve the use of newer techniques and reagents and can be more efficient and cost-effective.
    Some of the most popular modern synthesis methods for the synthesis of 2-chlorothieno[3,2-d]pyrimidine include the Nathan-Davis oxidation and the Mao-Suzuki reaction.
    These methods provide the desired product in good yield and are considered to be more efficient and cost-effective alternatives to classical synthesis methods.



    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.