What is the chemical structure 4-amino-5-chloro-2-ethoxy-N- {[4- (4-fluorobenzyl) morpholin-2-yl] methyl} benzamide 2-hydroxypropane-1,2,3-tricarboxylate (1:1)?

This compound, 4 - amino - 5 - chloro - 2 - ethoxy - N - {[4 - (4 - fluorobenzyl) morpholin - 2 - yl] methyl} benzamide 2 - hydroxypropane - 1,2,3 - tricarboxylate (1:1), consists of two parts.

One is 4 - amino - 5 - chloro - 2 - ethoxy - N - {[4 - (4 - fluorobenzyl) morpholin - 2 - yl] methyl} benzamide, the core structure of this part is benzamide. On the benzene ring, there is an amino group at the 4th position, a chlorine atom at the 5th position, and an ethoxy group at the 2nd position. The nitrogen atom of the amide group is connected to a complex side chain, and the side chain contains a morpholine ring. The morpholine ring is connected to 4-fluorobenzyl at the 4th position, and methylene at the 2nd position, which is then connected to benzamide.

The second is 2-hydroxypropane-1,2,3-tricarboxylate, that is, citrate ion (remove one hydrogen), which is combined with the above-mentioned benzamide part in a ratio of 1:1. The overall structure of this compound is ingenious, and the groups are connected to each other, or their chemical properties and biological activities are affected, presenting a unique chemical

What are the main uses of 4-amino-5-chloro-2-ethoxy-N- {[4- (4-fluorobenzyl) morpholin-2-yl] methyl} benzamide 2-hydroxypropane-1,2,3-tricarboxylate (1:1)?

4-Amino-5-chloro-2-ethoxy-N - {[4 - (4-fluorobenzyl) morpholine-2-yl] methyl} benzamide 2-hydroxypropane-1,2,3-tricarboxylate (1:1), this is a specific chemical substance. It has a wide range of uses and is commonly found in the field of pharmaceutical research and development.

In the process of pharmaceutical creation, this compound may have unique pharmacological activity. Or it can be used as a lead compound for researchers to further explore its interaction with specific targets in organisms. Through accurate analysis, it is expected to reveal its potential to treat specific diseases, such as the key signaling pathways involved in certain diseases, which can be modulated by the compound to achieve therapeutic purposes.

Furthermore, in the field of medicinal chemistry, the structural properties of this substance may provide inspiration for the design of more efficient and safe drugs. Researchers can skillfully modify and optimize its pharmacokinetic properties according to its structure, such as improving its absorption, distribution, metabolism and excretion characteristics in the body, or enhancing its selectivity and affinity for targets to reduce adverse reactions and improve therapeutic effects. < Br >
may also play an important role in preclinical research to evaluate the safety and efficacy of drugs, and to lay a solid foundation for subsequent clinical trials, with the aim of contributing to human health and well-being.

What are the physicochemical properties 4-amino-5-chloro-2-ethoxy-N- {[4- (4-fluorobenzyl) morpholin-2-yl] methyl} benzamide 2-hydroxypropane-1,2,3-tricarboxylate (1:1)?

This compound is 4-amino-5-chloro-2-ethoxy-N - {[4- (4-fluorobenzyl) morpholine-2-yl] methyl} benzamide 2-hydroxypropane-1,2,3-tricarboxylate (1:1). Its physical and chemical properties are as follows:

In appearance, or white to off-white crystalline powder, due to the interaction of various groups in its molecular structure, the whole exhibits a relatively regular crystalline form.

In terms of solubility, the compound should have a certain solubility in organic solvents, such as dimethyl sulfoxide (DMSO) and N, N-dimethylformamide (DMF). This is due to the interaction between the polar groups in the molecule and the organic solvent molecules, which can form forces such as hydrogen bonds or van der Waals forces; but the solubility in water may be relatively limited, although there are some polar parts, the hydrophobic part of the molecule as a whole is also more significant.

At the melting point, due to the existence of hydrogen bonds, van der Waals forces, and ionic bonds (carboxylate part) between molecules, the intermolecular bonding is relatively tight, and the estimated melting point is high. A specific temperature is required to destroy these forces to melt the compound. In terms of stability,

is relatively stable in dry and cool environments. However, in high temperature and high humidity environments, it may be unstable due to changes in some sensitive groups in the molecule, such as ester hydrolysis, aminoprotonation and other reactions. And if it comes into contact with strong oxidizing agents or reducing agents, the benzene ring, amine group, carboxyl group and other groups have certain redox activity, and corresponding redox reactions will occur, thus affecting its stability.

What are the key steps in the synthesis of 4-amino-5-chloro-2-ethoxy-N- {[4- (4-fluorobenzyl) morpholin-2-yl] methyl} benzamide 2-hydroxypropane-1,2,3-tricarboxylate (1:1)?

The key step in the synthesis of 4-amino-5-chloro-2-ethoxy-N-{ [4- (4-fluorobenzyl) morpholine-2-yl] methyl} benzamide 2-hydroxypropane-1,2,3-tricarboxylate (1:1) is like exploring the secret method in the ancient scrolls, which is related to whether this compound can be delicately produced.

The initial step may require careful construction of the skeleton of benzamide. Based on suitable halobenzoic acid, ethoxy is introduced through clever reaction with ethoxylating reagents, which is like adding a stable beam to the prototype structure. In this process, the reaction temperature, time, and the ratio of reagents all need to be precisely controlled, such as drawing delicate pictures between micro-particles.

Then, the introduction of amino groups is also the key. Or by means of the amination reaction, the halogen atom is replaced by an amino group. This step is like carving a delicate texture on the established structure. The mildness and accuracy of the conditions are essential, otherwise impurities are prone to occur, such as beautiful jade dust.

Furthermore, the part containing fluorobenzyl morpholine methyl is constructed. 4- (4-fluorobenzyl) morpholine is prepared first, and then it is reacted with a specific reagent to introduce methyl groups, which are then connected to the formed benzamide part. This is a delicate joint of synthesis. It is necessary to consider the reactivity and selectivity in detail. It is like a tenon-and-mortise joint, and there is no mistake at all.

Finally, a salt type of 2-hydroxypropane-1,2,3-tricarboxylate is formed. Through a suitable acid-base reaction, benzamide is combined with 2-hydroxypropane-1,2,3-tricarboxylic acid in a ratio of 1:1. This step requires attention to the pH of the reaction environment and the properties of the solvent, just like controlling the subtle rhythm, in order to play a pure synthetic movement.

4-amino-5-chloro-2-ethoxy-N- {[4- (4-fluorobenzyl) morpholin-2-yl] methyl} benzamide 2-hydroxypropane-1,2,3-tricarboxylate (1:1) market outlook?

4-Amino-5-chloro-2-ethoxy-N - {[4- (4-fluorobenzyl) morpholine-2-yl] methyl} benzamide 2-hydroxypropane-1,2,3-tricarboxylate (1:1), according to its name, this is a fine chemical compound. In the current market, its prospects are quite promising.

From the perspective of the pharmaceutical field, this compound has a unique structure or potential biological activity. Nowadays, there is a great demand for new compounds in pharmaceutical research and development. Many pharmaceutical companies and scientific research institutions are keen to explore substances with unique structures and functions in order to discover new drug targets and therapeutic methods. This compound may exhibit unique effects in the treatment of specific diseases, such as anti-tumor, anti-virus, etc. Because the pharmaceutical industry may have considerable attention to it, or has started related research and exploration. If the research and development goes well, it may become an important part of new drugs in the future, and then gain a place in the market.

In the chemical industry, it may be used as a special intermediate to synthesize more complex and high-value-added products. With the growing pursuit of product refinement and functionalization in the chemical industry, the demand for such special intermediates may be growing. If it can achieve large-scale production and ensure stable quality, it may occupy a key link in the chemical industry chain, bringing considerable economic benefits to chemical enterprises.

However, the road ahead for its market is not smooth sailing. The complexity of the synthesis process may lead to high production costs, which is a major challenge for commercialization and promotion. And the market competition is fierce, and it is necessary to compete with similar or similar products. To gain a foothold in the market, we must make more efforts in technological innovation, cost control, quality improvement, etc., in order to adapt to market changes and open up broad prospects.