The product Ethyl 3- (2- ((4-carbamimidoylphenyl) amino) methyl) -1-methyl-N- (pyridin-2-yl) -1H-benzo [d] imidazole-5-carboxamido) propanoate what is the chemical structure

Alas, this is a question about the chemical structure of "Ethyl 3- (2- (((4-carbamimidoylphenyl) amino) methyl) -1-methyl-N- (pyridin-2-yl) -1H-benzo [d] imidazole-5-carboxamido) propanoate". The name of this compound is long and complicated, and its structure is deduced according to its name, and each part needs to be analyzed in detail. "Ethyl" is ethyl, that is, -C 2O H, which is often one of the ester groups. In "3- (2- (((4-carbamimidoylphenyl) amino) methyl) -1-methyl-N- (pyridin-2-yl) -1H-benzo [d] imidazole-5-carboxamido) propanoate", "propanoate" is a propanoate structure, indicating the presence of -COO-linked ethyl groups. " 1H-benzo [d] imidazole "is the core structure of benzimidazole, with a benzene ring fused to the imidazole ring." 1-methyl "means that the benzimidazole ring has a methyl substitution at 1 position;" 5-carboxamido "shows that the benzimidazole ring has a formamide group at 5 position -CONH." 2 - ((4 - carbamimidoylphenyl) amino) methyl) "means that the 2 position of the benzimidazole ring is connected to an amino-NH - via methylene-CH -2 -, which in turn is connected to 4-amidophenyl." N- (pyridin-2-yl) "indicates that the nitrogen atom of the formamide group is attached to the pyridine-2-yl group. Overall, the structure of this compound is composed of ethyl propionate ester group and benzimidazole ring as the core, with specific substituents in many places on the ring and connecting other groups. It is like a well-constructed chemical molecular building, and each part is connected according to specific rules to construct a unique chemical structure.

What are the main uses of Ethyl 3- (2- ((4-carbamimidoylphenyl) amino) methyl) -1-methyl-N- (pyridin-2-yl) -1H-benzo [d] imidazole-5-carboxamido) propanoate

Ethyl+3-%282-%28%28%284-carbamimidoylphenyl%29amino%29methyl%29-1-methyl-N-%28pyridin-2-yl%29-1H-benzo%5Bd%5Dimidazole-5-carboxamido%29propanoate is a complex organic compound with a long name and complex structure. Such compounds have a wide range of uses in the field of drug development and organic synthesis.

In drug development, this compound may have unique biological activities. The different groups contained in its structure can interact with specific targets in organisms. For example, the 4-carbamimidoylphenyl part may exhibit high affinity for certain enzymes or receptors, thereby regulating related biological processes or laying the foundation for the development of new therapeutic drugs. In the development of anti-tumor drugs, such compounds can be used to bind to specific targets of tumor cells to interfere with tumor cell growth, proliferation or metastasis, providing new ways to combat cancer.

In the field of organic synthesis, it can serve as a key intermediate. Its complex structure provides organic chemists with many reaction check points, and through ingenious design of reaction routes, a series of compounds with diverse structures can be derived. For example, by modifying its specific groups, such as further optimization of the esterification reaction of the propanoate part, or functionalization of the benzo [d] imidazole ring, more characteristic and functional organic molecules can be synthesized, providing rich structural units for materials science, total synthesis of natural products and other fields, and promoting the continuous development of organic synthetic chemistry.

What is the synthesis method of Ethyl 3- (2- ((4-carbamimidoylphenyl) amino) methyl) -1-methyl-N- (pyridin-2-yl) -1H-benzo [d] imidazole-5-carboxamido) propanoate

Ethyl 3- (2- ((4-carbamimidoylphenyl) amino) methyl) -1-methyl-N- (pyridin-2-yl) -1H-benzo [d] imidazole-5-carboxamido) propanoate is a complex organic compound. To synthesize this compound, the following ancient methods can be followed:

The key intermediates need to be prepared first to build the core structure of the molecule. For the benzimidazole part, it can be obtained by condensation and cyclization of suitable o-phenylenediamine derivatives with corresponding carboxylic acids or their derivatives under suitable reaction conditions. For example, select a suitable substituted o-phenylenediamine, and a specific carboxyl-containing compound, under the catalysis of acid or base, heat the reaction to promote the condensation of the amino group with the carboxyl group, and then close the ring to form a benzimidazole ring.

For 4-carbamimidoylphenyl fragments, it can be obtained by functional group conversion of aniline compounds. For example, using p-nitroaniline as a starting material, the nitro group is first converted into an amino group by reduction reaction, and then reacted with cyanamide or related amidination reagents to introduce the amidine functional group.

Then, the intermediate containing benzimidazole is connected to the 4-carbamimidoylphenyl fragment. Strategies of nucleophilic substitution or coupling reactions can be used to combine the two. If there is a suitable halogen or active intermediate, a nucleophilic substitution reaction can occur under the action of a base to achieve the formation of carbon-nitrogen bonds.

After the core structure is constructed, the remaining substituents such as pyridine-2-group and ester group are introduced into it. For pyridine-2-group, pyridine-2-group can be introduced to a suitable reaction check point by means of coupling reactions catalyzed by transition metals, such as Buchwald-Hartwig reaction. The ester group can be obtained by esterification of the corresponding carboxylic acid and ethanol under acid catalysis.

The whole synthesis process requires fine control of the reaction conditions of each step, such as temperature, reaction time, ratio of reactants and amount of catalyst, etc., and strict separation and purification of the product at each step is required to ensure the purity and yield of the final product, so as to achieve Ethyl 3- (2- ((4-carbamimidoylphenyl) amino) methyl) -1-methyl-N- (pyridin-2-yl) -1H-benzo [d] imidazole-5-carboxamido) propanoate synthesis.

Ethyl 3- (2- ((4-carbamimidoylphenyl) amino) methyl) -1-methyl-N- (pyridin-2-yl) -1H-benzo [d] imidazole-5-carboxamido) propanoate

This "Ethyl+3-%282-%28%28%284-carbamimidoylphenyl%29amino%29methyl%29-1-methyl-N-%28pyridin-2-yl%29-1H-benzo%5Bd%5Dimidazole-5-carboxamido%29propanoate" is a complex organic compound. Considering the market prospect, it needs to be explored many times.

It may emerge in the field of pharmaceutical research and development. In today's pharmaceutical industry, there is a high enthusiasm for the exploration of new compounds, hoping that it can become a key component in the development of new drugs. This compound has a unique structure or specific biological activity, and can target disease-related targets. If it can be accurately developed, it may have major breakthroughs in the treatment of diseases, such as cancer and neurological diseases. The market potential cannot be underestimated.

However, if it wants to thrive in the market, it also faces many difficulties and obstacles. The first one is the problem of the synthesis process. To produce on a large scale, it is necessary to optimize the synthesis path, improve the yield and reduce the cost. This compound is complex in structure and difficult to synthesize. If there is no effective breakthrough in the synthesis process and the production cost remains high, its marketing activities will be limited.

Furthermore, safety and efficacy verification are also crucial. Although it may have potential in theory, it needs to undergo rigorous clinical trials to prove that it is safe and effective in humans. This process is long and expensive. If it cannot pass rigorous tests, it will not be able to enter the market even if the structure is exquisite.

In addition, market competition should not be underestimated. There are many experts in the field of pharmaceutical research and development, and similar or potential replacement compounds are emerging one after another. If it cannot stand out in terms of research and development progress, cost control, and efficacy advantages, it may be eliminated by the market.

From a comprehensive perspective, although "Ethyl+3-%282-%28%28%284-carbamimidoylphenyl%29amino%29methyl%29-1-methyl-N-%28pyridin-2-yl%29-1H-benzo%5Bd%5Dimidazole-5-carboxamido%29propanoate" has addressable market opportunities, the road ahead is full of thorns, and it is necessary for scientific research and market personnel to work together to break through many difficulties in order to have the opportunity to shine in the market.

Ethyl 3- (2- ((4-carbamimidoylphenyl) amino) methyl) -1-methyl-N- (pyridin-2-yl) -1H-benzo [d] imidazole-5-carboxamido) propanoate

Ethyl 3- (2- ((4-carbamimidoylphenyl) amino) methyl) -1-methyl-N- (pyridin-2-yl) -1H-benzo [d] imidazole -5-carboxamido) propanoate is a complex organic compound. When it comes to the safety precautions related to this compound, it is as if you need to choose carefully if you are going astray.

Its chemical structure is complex, or it has special chemical activity and reactivity. When operating, it is first necessary to ensure that it is carried out in a well-ventilated place. Due to the accumulation of volatiles in a closed space, or the irritation of the respiratory tract, and even the risk of poisoning. Like being in an airtight room, the turbid air is difficult to disperse, and the harmful gas gradually accumulates, endangering the body.

Furthermore, this compound may be irritating to the skin and eyes. Therefore, when coming into contact, you must wear appropriate protective equipment, such as gloves, goggles, etc. If you accidentally touch the skin, you should immediately rinse with a lot of water, just like stains, and quickly wash with water to avoid penetrating into the skin. If it enters the eyes, you should quickly rinse with running water and seek medical attention in time without delay.

Because it is a chemical compound or has potential biological toxicity. After operation, be sure to thoroughly clean your hands and utensils to prevent residual substances from contaminating other objects or the entrance. Just like after work, wash the dust and feel at ease. And when storing, it needs to be placed in a cool, dry place away from fire sources and oxidants. Due to improper storage or the deterioration, combustion or even explosion of compounds, it is like placing the flame next to flammable materials, and the danger is imminent.

Before use, it is also necessary to read the relevant chemical safety technical instructions carefully to fully understand its nature, hazards and emergency treatment methods, so that in the face of various situations, it can be handled easily and operate safely.