N-{2-[bis(1-methylethyl)amino]ethyl}-2-{[(2-hydroxy-4,5-dimethoxyphenyl)carbonyl]amino}-1,3-thiazole-4-carboxamide

This is an organic compound, and its name is N- {2- [bis (1-methylethyl) amino] ethyl} -2- {[ (2-hydroxy-4,5-dimethoxyphenyl) carbonyl] amino} -1, 3-thiazole-4-carboxamide. To clarify its chemical structure, we should name it according to its name.
Concept its name, "N- {2- [bis (1-methylethyl) amino] ethyl}", which is a substituent attached to the nitrogen atom. For "bis (1-methylethyl) amino", diisopropylamino is also, this amino group is attached to the ethyl group. " 2- {[ (2-hydroxy-4,5-dimethoxyphenyl) carbonyl] amino} ", this part refers to the structure of a 2-hydroxy-4,5-dimethoxybenzoyl group connected to an amino group at the second position of the main chain of the compound." 1,3-thiazole-4-carboxamide ", indicating that the main chain of the compound is a thiazole ring, and there is a carboxamide group at the 4th position.
In summary, this compound has a thiazole ring as the core and a carboxamide group at the 4th position; a structure containing a 2-hydroxy-4,5-dimethoxybenzoyl amino group at the 2nd position; an ethyl group containing diisopropylamino is attached to the nitrogen atom. Its chemical structure is complex, and the groups are interconnected to form the unique structure of this organic compound.

This compound is named N- {2- [bis (1-methylethyl) amino] ethyl} -2- { (2-hydroxy-4,5-dimethoxyphenyl) carbonyl] amino} -1, 3-thiazole-4-carboxamide, and its main uses are as follows:
This compound may have important functions in the field of medical research. Looking at its structure, it contains a specific group combination, or has the potential to interact with targets in vivo. For example, the thiazole ring and amide group in its structure are often the key check points for binding to biological macromolecules such as proteins and enzymes in many past studies. Therefore, it is speculated that this compound may be used as a lead compound, optimized and modified to develop drugs for treating specific diseases.
Furthermore, this compound can be used as an important model in the study of the structure-activity relationship of medicinal chemistry. By changing and modifying different substituents in its structure, the effect of structural changes on biological activity is explored, thus laying the foundation for the design and synthesis of more efficient and low-toxicity new drugs.
In biological activity screening experiments, it can serve as a research tool to explore new biological activity mechanisms and action pathways. With the study of the activity of this compound in cell models or animal models, it may be able to reveal unrecognized biological processes, contributing to the basic research of life science.

The synthesis process of this substance is as follows: To obtain N- {2- [bis (1-methylethyl) amino] ethyl} -2- { (2-hydroxy-4,5-dimethoxyphenyl) carbonyl] amino} -1,3-thiazole - 4 - carboxamide, a multi-step reaction is required.
The first step is to use 2-hydroxy-4,5-dimethoxybenzoic acid as the starting material and heat it with an appropriate chlorination reagent, such as thionyl chloride. In this step, the antique method uses a kettle as a device and fire as the source to heat the two in the kettle. The benzoic acid carboxyl group is converted into an acid chloride to obtain 2-hydroxy-4,5-dimethoxybenzoyl chloride. This step requires temperature control and control to prevent side reactions.
Next, take 2-amino-4-thiazole formamide and the resulting acid chloride, react in a suitable organic solvent such as dichloromethane in the presence of an acid binding agent, such as triethylamine, and the two are mixed in the vessel according to the ancient method. The acid binding agent helps to remove the acid and react to generate 2- { (2-hydroxy-4,5-dimethoxyphenyl) carbonyl] amino} -1,3-thiazole-4-carboxylamide.
Step by step, N, N-diisopropyl ethylenediamine is reacted with the above product. In this step, an appropriate solvent, such as N, N-dimethylformamide, is used as a medium to heat and promote the reaction. According to the ancient method, by borrowing the temperature of fire, the two are fully intermingled to obtain the target product N- {2- [bis (1-methylethyl) amino] ethyl} -2- {[ (2-hydroxy-4,5-dimethoxyphenyl) carbonyl] amino} -1,3-thiazole-4-carboxylamide. Each step of the reaction requires separation and purification methods, such as extraction, column chromatography, etc., to obtain high-purity products.

There is a substance called N- {2- [bis (1-methylethyl) amino] ethyl} -2- {[ (2-hydroxy-4,5-dimethoxyphenyl) carbonyl] amino} -1, 3-thiazole-4-carboxamide. In the market prospect of this substance, I will come to you one by one.
In the field of Guanfu medicine, this substance may have unique pharmacological activities. Its structure is exquisite, and the chemical groups involved may interact with specific targets in the body. For example, the thiazole structure is often seen in antibacterial and anti-inflammatory drugs, or suggests that this substance has potential effects in the treatment of related diseases. If it is properly developed, made into drugs, and put on the market, it may be able to get a share of the market for antibacterial and anti-inflammatory drugs.
Furthermore, in the field of scientific research, the unique structure of this substance can provide new ideas and directions for the study of organic synthetic chemistry. Scientists can use this substance as a blueprint to explore the synthesis path of new compounds and develop more biologically active substances. Therefore, in the scientific research reagent market, there may also be a certain demand.
However, its market prospects are not entirely smooth. The process of synthesizing this substance may be complicated and expensive. If efficient and economical synthesis methods cannot be found, its large-scale production and marketing activities will be hindered. And drug development must undergo rigorous clinical trials to prove its safety and efficacy. This process is long and expensive, and if there is a little mistake, all efforts will be wasted.
In summary, N- {2- [bis (1-methylethyl) amino] ethyl} -2- {[ (2-hydroxy-4,5-dimethoxyphenyl) carbonyl] amino} -1, 3-thiazole-4-carboxamide in the pharmaceutical and scientific research market, although there are potential opportunities, but also face many challenges. Only by overcoming the problems of synthesis and research and development can we emerge in the market and seek opportunities for development.

This medicine is called N- {2- [bis (1-methylethyl) amino] ethyl} -2- { (2-hydroxy-4,5-dimethoxyphenyl) carbonyl] amino} -1, 3-thiazole-4-carboxamide, but I don't know its exact corresponding Han name. Although I don't know the details, all medicines have their advantages and disadvantages, and this medicine should also have related side effects and risks.
The side effects of husband medicine, or disturb the body. Light or cause gastrointestinal discomfort, such as nausea, vomiting, abdominal pain, diarrhea, all of which are due to drug entry into the body, disturbing the transportation of the stomach. Or cause dizziness, headache, affect people's consciousness, make confusion, inconvenience. Or there may be allergies, skin rashes and itching, even involving breathing, causing shortness of breath, endangering life.
As for the risk, or with other drugs. If taken improperly, the drug interaction, or toxic side effects, or reduce the effect of the drug, so that the effectiveness of the cure will not be possible. And long-term use may cause the body to resist the drug, and the effectiveness of the drug will gradually decrease. Or for specific groups of people, such as pregnant women, the elderly and the weak, and children, because their bodies are different from ordinary people, the risk of drug use is particularly high, or damage the fetal essence, or damage the righteousness. Therefore, when taking medication, we should carefully review the situation, weigh the pros and cons, follow the doctor's advice, and do not act rashly to avoid harm.