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    Home > Active Ingredient News > Drugs Articles > The Instruction of 7-chloro-5-(4-hydroxyphenyl)-1,3-dihydro-1,4-benzodiazepin-2-one

    The Instruction of 7-chloro-5-(4-hydroxyphenyl)-1,3-dihydro-1,4-benzodiazepin-2-one

    • Last Update: 2023-05-11
    • Source: Internet
    • Author: User
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    In the chemical industry, the production and use of various chemical compounds is a common sight.
    One such compound is 7-chloro-5-(4-hydroxyphenyl)-1,3-dihydro-1,4-benzodiazepin-2-one, which is commonly referred to as chlorpheniramine maleate.
    This compound is used as a pharmaceutical intermediate and as a raw material in the production of various drugs.


    The production of chlorpheniramine maleate involves several steps, which are discussed in detail below.


    Step 1: Synthesis of 7-chloro-5-(4-hydroxyphenyl)-1,3-dihydro-1,4-benzodiazepin-2-one
    The synthesis of chlorpheniramine maleate begins with the synthesis of its parent compound, 7-chloro-5-(4-hydroxyphenyl)-1,3-dihydro-1,4-benzodiazepin-2-one.
    This compound can be synthesized using various methods, but the most common method is the condensation of 7-chloro-5-nitro-1,3-dihydro-1,4-benzodiazepin-2-one with 4-hydroxyphenylacetone in the presence of a strong acid catalyst.


    Step 2: Nitration of 7-chloro-5-(4-hydroxyphenyl)-1,3-dihydro-1,4-benzodiazepin-2-one
    After the synthesis of 7-chloro-5-(4-hydroxyphenyl)-1,3-dihydro-1,4-benzodiazepin-2-one, it is subsequently nitrated using nitric acid to produce 7-chloro-5-(4-nitrophenyl)-1,3-dihydro-1,4-benzodiazepin-2-one.


    Step 3: Hydrolysis of 7-chloro-5-(4-nitrophenyl)-1,3-dihydro-1,4-benzodiazepin-2-one
    The next step involves the hydrolysis of 7-chloro-5-(4-nitrophenyl)-1,3-dihydro-1,4-benzodiazepin-2-one using a strong acid, such as hydrochloric acid, to produce 7-chloro-5-(4-hydroxyphenyl)-1,3-dihydro-1,4-benzodiazepin-2-one.


    Step 4: Methylation of 7-chloro-5-(4-hydroxyphenyl)-1,3-dihydro-1,4-benzodiazepin-2-one
    The final step in the synthesis of chlorpheniramine maleate involves the methylation of 7-chloro-5-(4-hydroxyphenyl)-1,3-dihydro-1,4-benzodiazepin-2-one using a methylating agent, such as methyl iodide, in the presence of a polar solvent, such as ether.
    This leads to the formation of chlorpheniramine maleate.


    Chlorpheniramine maleate can be synthesized using various methods, but the above-described method is the most common method used in industry.
    The synthesis of chlorpheniramine maleate requires the use of various chemical reagents and solvents, and the entire process is usually carried out under carefully controlled conditions to ensure the purity and quality of the final product.


    Applications of Chlorpheniramine Maleate
    Chlorpheniramine maleate is used as a pharmaceutical intermediate and as a raw material in the production of various drugs.
    It is commonly used as an antihistamine and as a sedative in the treatment of allergy symptoms and insomnia.
    It is also used in the treatment of anxiety disorders and as a muscle relaxant.


    In addition to its pharmaceutical applications, chlorphen


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