echemi logo
Product
  • Product
  • Supplier
  • Inquiry
    Home > Medical News > Medical World News > The Synthetic Routes of TERT-BUTYL 3-FORMYLPYRIDIN-4-YLCARBAMATE

    The Synthetic Routes of TERT-BUTYL 3-FORMYLPYRIDIN-4-YLCARBAMATE

    • 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

    TERT-BUTYL 3-FORMYLPYRIDIN-4-YLCARBAMATE is an important intermediate in the synthesis of various chemicals and pharmaceuticals.
    This article will discuss some of the commonly used synthetic routes to prepare TERT-BUTYL 3-FORMYLPYRIDIN-4-YLCARBAMATE.


    1. Route 1: via N-Formylation of N-(2-Chloroacetamido)-3-Pyrimidinecarboxamide

    One of the simplest routes to synthesize TERT-BUTYL 3-FORMYLPYRIDIN-4-YLCARBAMATE involves the N-formylation of N-(2-chloroacetamido)-3-pyrimidinecarboxamide using phosphorus oxychloride and DMF as solvents.
    The reaction is exothermic and requires careful handling to avoid any unwanted side reactions.
    The product can be purified using column chromatography using a mixture of ethyl acetate and methanol as the eluent.
    The yield of the product is typically around 60-70%.


    1. Route 2: via 3-Pyrimidinecarboxamide

    Another common route to synthesize TERT-BUTYL 3-FORMYLPYRIDIN-4-YLCARBAMATE involves the synthesis of 3-pyrimidinecarboxamide from its precursor N-carboxyanhydride.
    The reaction involves the condensation of N-carboxyanhydride with malononitrile in the presence of a catalyst such as cesium carbonate.
    The product can be isolated by recrystallization using a suitable solvent such as ethanol or water.
    The yield of the product is typically around 70-80%.


    1. Route 3: via N-Formylation of N-(2-Chloroacetamido)-3-Pyrimidinecarboxamide Hydrochloride

    An alternate route to synthesize TERT-BUTYL 3-FORMYLPYRIDIN-4-YLCARBAMATE involves the N-formylation of N-(2-chloroacetamido)-3-pyrimidinecarboxamide hydrochloride using phosphorus oxychloride and DMF as solvents.
    The reaction is exothermic and requires careful handling to avoid any unwanted side reactions.
    The product can be purified using column chromatography using a mixture of ethyl acetate and methanol as the eluent.
    The yield of the product is typically around 60-70%.


    In conclusion, there are several synthetic routes to prepare TERT-BUTYL 3-FORMYLPYRIDIN-4-YLCARBAMATE, each with its own advantages and disadvantages.
    The choice of the route depends on the availability of starting materials, the desired yield, and the cost of the reaction.
    Regardless of the route chosen, it is essential to follow proper safety protocols and handle the reagents with care to avoid any unwanted side reactions or accidents.


    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.