3 4 Bis Cyclopropylmethoxy N 3 5 Dichloropyridine 4 Yl Benzamide
pyridine pyrrole pyrazine piperidine piperazine

3,4-bis(cyclopropylmethoxy)-n-(3,5-dichloropyridine-4-yl)benzamide

    Specifications

    HS Code

    776754

    Chemical Name 3,4-bis(cyclopropylmethoxy)-N-(3,5-dichloropyridine-4-yl)benzamide
    Molecular Formula C21H20Cl2N2O3
    Molecular Weight 419.299 g/mol
    Appearance Solid (usually)

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    Where to Buy 3,4-bis(cyclopropylmethoxy)-n-(3,5-dichloropyridine-4-yl)benzamide in China?
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    As a leading 3,4-bis(cyclopropylmethoxy)-n-(3,5-dichloropyridine-4-yl)benzamide supplier, we deliver high-quality products across diverse grades to meet evolving needs, empowering global customers with safe, efficient, and compliant chemical solutions.

    What are the main application fields of 3,4-bis (cyclopropylmethoxy) -N- (3,5-dichloropyridine-4-yl) benzamide
    3% 2C4-bis (cyclopropyl methoxy) -N- (3,5-difluoropyridine-4-yl) benzamide, which has important applications in the field of pharmaceutical research and development.
    In the current way of pharmaceutical creation, it is the important task of many doctors and pharmacists to explore new drugs with high efficiency and low toxicity. This compound has emerged in the development of targeted drugs due to its unique molecular structure. The ingenious combination of cyclopropyl methoxy and difluoropyridine gives it specific physicochemical properties and biological activities.
    To observe the ravages of cancer, targeted therapy drugs have brought vitality to many patients. 3% 2C4-bis (cyclopropylmethoxy) -N- (3,5-difluoropyridine-4-yl) benzamide may be targeted at specific targets of cancer cells, with precise force, inhibiting the proliferation, invasion and metastasis of cancer cells. Taking lung cancer as an example, after many experiments, it has been found that it can bind to a key protein on the surface of lung cancer cells, block the transmission of cancer cell growth signals, and then induce cancer cell apoptosis.
    Not only this, but also in the field of treatment of inflammatory diseases. Inflammation originates from the overactivation of immune cells in the body, which triggers the release of a large number of inflammatory mediators. This compound can regulate the activity of immune cells, reduce the secretion of inflammatory mediators, and effectively relieve inflammatory symptoms. In animal experiments on rheumatoid arthritis, after administration of this compound, symptoms such as joint swelling and pain were significantly improved.
    In summary, 3% 2C4-bis (cyclopropylmethoxy) -N- (3,5-difluoropyridine-4-yl) benzamide has great potential in the field of medicine and is expected to bring new opportunities for the treatment of more diseases.
    What are the synthesis methods of 3,4-bis (cyclopropylmethoxy) -N- (3,5-dichloropyridine-4-yl) benzamide
    To prepare 3% 2C4-bis (epoxypropyloxy) -N- (3,5-difluoropyridine-4-yl) benzamide, the method is as follows:
    First, select the raw material. When the appropriate 3,5-difluoro-4-aminopyridine, 3,4-dihydroxybenzoic acid, etc. are taken as the starting materials, the two are the foundation of the reaction, and the purity and quality of the product are related to the quality.
    times, to form esters. The 3,4-dihydroxybenzoic acid reacts with epoxy chloropropane under the catalysis of base. Alkalis, such as sodium hydroxide, potassium hydroxide, etc., can promote the nucleophilic substitution of the two to form 3,4-bis (epoxy propyloxy) benzoate. During the reaction, it is essential to control the temperature and time, usually at an appropriate temperature, such as 50-80 degrees Celsius, and the number of reactions, in order to ensure the complete reaction.
    Then, amide. The resulting esters are combined with 3,5-difluoro-4-aminopyridine in a suitable solvent, such as dichloromethane, N, N-dimethylformamide, and assisted by a condensing agent, such as dicyclohexyl carbodiimide (DCC), 1-ethyl-3- (3-dimethylaminopropyl) carbodiimide hydrochloride (EDCI), etc., for amidation. The reaction environment should be anhydrous, and the temperature should be between room temperature and 50 degrees Celsius. After several reactions, the target product 3% 2C4-bis (epoxypropyloxy) -N- (3,5-difluoropyridine-4-yl) benzamide can be obtained.
    After the reaction is completed, it needs to be separated and purified. The column chromatography method can be used to use silica gel as the stationary phase to select a suitable eluent, such as a mixture of petroleum ether and ethyl acetate, eluted in different proportions, and the pure product can be separated; the recrystallization method can also be used to select a suitable solvent, such as ethanol, acetone, etc. After the product is dissolved, the crystallization is cooled to obtain a pure 3% 2C4-bis (epoxypropyloxy) -N- (3,5-difluoropyridine-4-yl) benzamide.
    What are the physicochemical properties of 3,4-bis (cyclopropylmethoxy) -N- (3,5-dichloropyridine-4-yl) benzamide
    3% 2C4-bis (epoxypropyloxy) -N- (3,5-difluoropyridine-4-yl) benzamide, which is a fine chemical obtained from organic synthesis. In terms of its physical and chemical properties, it is the key to study the properties of organic compounds.
    First of all, its physical properties. At room temperature, this substance may be in a solid state and have a specific crystal structure. Its melting point, boiling point and other properties are determined by the intermolecular forces and structures. The intermolecular structure of cycloxypropyloxy interacts with benzamide to form hydrogen bonds and van der Waals forces between molecules, which in turn affect its phase state and melting boiling point. After experimental determination, the exact melting point value may be obtained, which is the basis for identification and separation and purification.
    Let's talk about its chemical properties again, because it contains epoxy propyl oxide group, it has active reactivity. Epoxy ring is vulnerable to attack by nucleophilic reagents and undergoes ring-opening reaction. In contact with nucleophilic reagents such as water, alcohol, amine, etc., epoxy ring can be opened to generate corresponding addition products. This property makes it widely used in the field of organic synthesis, which can be used to prepare a variety of functional materials, pharmaceutical intermediates, etc. And because it contains fluoropyridyl groups, fluorine atoms have high electronegativity, which endows molecules with unique electronic effects. This not only affects the polarity of molecules, but also affects their chemical reactivity and stability. In reactions such as nucleophilic substitution and electrophilic substitution, the density of the electron cloud around the fluorine atom changes, which makes the reaction check point and reactivity different from that of conventional pyridine derivatives.
    In addition, the solubility of this substance is also an important physicochemical property. It may have good solubility in common organic solvents such as dichloromethane, N, N-dimethylformamide, but poor solubility in water. This is closely related to the polarity and structure of the molecule. Polar organic solvents form a similar miscibility with molecules, so that they can participate in reactions and separation operations in organic synthesis reaction systems.
    How competitive is 3,4-bis (cyclopropylmethoxy) -N- (3,5-dichloropyridine-4-yl) benzamide in the market?
    3% 2C4-bis (cyclopropylmethoxy) -N- (3,5-difluoropyridine-4-yl) benzamide is a competitive product in the market, which is related to many factors.
    Looking at its physical properties, if its properties are stable, its melting and boiling point is suitable, and its solubility is good, it can be well dispersed in various solvents, which will be conducive to its effectiveness in different reaction systems or application scenarios, so the competitiveness can be increased. If its stability is poor, it is easily deteriorated due to external factors such as temperature and humidity, light, etc., the competitiveness will be damaged.
    When it comes to the preparation process, if the synthesis route is simple and efficient, the raw materials are easy to obtain, the cost is low, and the reaction conditions are mild, the equipment requirements are not harsh, and the energy consumption is also low, this can greatly reduce the production cost. If the cost is low, it will be more flexible in market pricing, and it can attract many customers by virtue of the price advantage, and the competitiveness can be improved. On the contrary, if the preparation process is complicated, the raw materials are scarce and expensive, the reaction conditions are harsh, the production is difficult and the cost is high, it will be at a disadvantage in the market competition.
    Looking at the application field, if the compound has a unique and extensive use in the fields of pharmaceutical research and development, pesticide creation or material science, it can be used as a key intermediate to synthesize special drugs, high-efficiency pesticides, or give materials special properties, the market demand will be strong. If the demand is large, it will naturally be more competitive in the market. On the contrary, if the application field is narrow and the use is single, the market space will be limited and the competitiveness will be difficult to highlight.
    In addition, the supply and demand relationship in the market also affects its competitiveness. If the market demand for this product continues to grow, but the supply is relatively insufficient, its price may rise, and the profit margin of enterprises will increase, which can also stimulate production and enhance competitiveness. On the contrary, if the market oversupply, prices may fall, companies need to rely on quality, cost and other advantages to stand.
    This 3% 2C4 -bis (cyclopropylmethoxy) -N- (3,5 -difluoropyridine-4 -yl) benzamide in the market competitiveness, need to consider the physical properties, preparation process, application field and supply and demand relationship and other ends, in order to understand.
    What is the development prospect of 3,4-bis (cyclopropylmethoxy) -N- (3,5-dichloropyridine-4-yl) benzamide?
    3% 2C4-bis (cyclopropyl methoxy) -N- (3,5-difluoropyridine-4-yl) benzamide, which is a product in the field of organic synthesis. In today's chemical research and chemical industry, organic synthesis is progressing rapidly, and new compounds are emerging one after another. This compound also has specific research and development prospects.
    Looking at its structure, cyclopropyl methoxy is connected to benzamide, and difluoropyridine is introduced, which gives it unique physical and chemical properties. In the direction of pharmaceutical research and development, such fluoropyridine and cyclopropyl compounds often have good biological activity and pharmacokinetic properties. Or it can be modified and optimized to become a potential drug lead compound. After in-depth pharmacological research and clinical trials, it may be expected to be developed into a new type of drug for the treatment of specific diseases.
    In the field of materials science, the structure of the compound may give it unique electrical and optical properties, which can be used to develop new organic electronic materials, such as organic semiconductors, photoelectric conversion materials, etc., providing the possibility for miniaturization and high efficiency of electronic devices.
    However, its development also faces challenges. The problems of cumbersome synthesis process or existing steps and low yield require chemists to study better synthesis routes to improve efficiency and economy. At the same time, it is also indispensable for its biosafety and Environmental Impact Assessment to ensure that the application process is not harmful to the human body and the environment.
    Over time, through the unremitting exploration and innovation of researchers, 3% 2C4-bis (cyclopropylmethoxy) -N- (3,5-difluoropyridine-4-yl) benzamide may emerge in the fields of medicine and materials, contributing to the progress of human society.