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    Home > Medical News > Medical World News > The Production Process of 5-Bromo-2-chloro-7H-pyrrolo[2,3-d]pyrimidine

    The Production Process of 5-Bromo-2-chloro-7H-pyrrolo[2,3-d]pyrimidine

    • Last Update: 2023-05-06
    • Source: Internet
    • Author: User
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    The Production Process of 5-Bromo-2-chloro-7H-pyrrolo[2,3-d]pyrimidine in the Chemical Industry


    5-Bromo-2-chloro-7H-pyrrolo[2,3-d]pyrimidine, also known as Br-CPP, is a synthetic organic compound that is mainly used as an intermediate in the production of various chemicals and pharmaceuticals.
    The compound is important in the production process of several important drugs, including anti-cancer and antiviral medications.


    The production process of Br-CPP involves several stages, including synthesis, purification, and characterization.
    The following is a detailed overview of the production process of Br-CPP in the chemical industry.


    Stage 1: Synthesis of 2-chloro-5-bromo-7H-pyrrolo[2,3-d]pyrimidine


    The synthesis of 2-chloro-5-bromo-7H-pyrrolo[2,3-d]pyrimidine is the first step in the production of Br-CPP.
    The synthesis process involves several steps, including the following:


    • Treatment of N-bromosuccinimide with 2-chloropyrimidine-5-boronic acid in the presence of a catalyst such as cesium carbonate to form N-bromosuccinimide-2-chloropyrimidine-5-boronic acid.
    • Hydrolysis of the resulting product with a strong acid, such as hydrochloric acid, to yield 2-chloro-5-bromo-7H-pyrrolo[2,3-d]pyrimidine.

    The synthesis process typically involves the use of various chemical reagents, solvents, and catalysts, which may vary depending on the manufacturer's specific process.


    Stage 2: Purification of 2-chloro-5-bromo-7H-pyrrolo[2,3-d]pyrimidine


    After the synthesis of 2-chloro-5-bromo-7H-pyrrolo[2,3-d]pyrimidine, the resulting product must be purified to remove any impurities that may have been introduced during the synthesis process.
    The purification process typically involves several steps, including the following:


    • Crystallization of the crude product with a suitable solvent, such as ethanol or water, to yield a pure crystalline form of the compound.
    • Recrystallization of the resulting crystals with a second solvent, such as dichloromethane or ethyl acetate, to remove any remaining impurities.
    • Chromatography, either by high-performance liquid chromatography (HPLC) or by gas chromatography (GC), to further purify the resulting product.

    The purification process is critical to the production of Br-CPP, as any impurities present in the final product may affect its efficacy or safety.


    Stage 3: Characterization of Br-CPP


    After the purification of Br-CPP, the compound must be characterized to determine its chemical properties and to confirm its purity.
    The characterization process typically involves several steps, including the following:


    • Spectroscopic analysis, such as infrared spectroscopy (IR) or nuclear magnetic resonance spectroscopy (NMR), to determine the molecular structure of Br-CPP.
    • Thermal analysis, such as thermogravimetry (TG) or derivative thermogravimetry (DTG), to study the thermal stability of Br-CPP.
    • Chromatographic analysis, as mentioned earlier, to confirm the purity of the compound.

    The


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