2-(5-Isopropyl-5-methyl-4-oxo-2-imidazolin-2-yl)-3-quinolinecarboxylic acid

This is the chemical name of 2- (5-isopropyl-5-methyl-4-oxo-2-imidazoline-2-yl) -3-quinoline carboxylic acid. To clarify its chemical structure, it is necessary to analyze the structural information contained in this name in detail.
"Quinoline carboxylic acid" shows that its core structure is a quinoline ring with a carboxyl group at the 3rd position. The quinoline ring is a nitrogen-containing fused heterocyclic ring, which is formed by fusing a benzene ring with a pyridine ring.
"2- (5-isopropyl-5-methyl-4-oxo-2-imidazoline-2-yl) " table is connected to an imidazoline derivative at the 2nd position of the quinoline ring. This imidazoline ring has the following characteristics: the 5th position is connected to isopropyl and methyl, the 4th position is oxo (ie carbonyl), and the 2nd position is connected to the quinoline ring.
The isopropyl group is obtained by removing one terminal hydrogen from propane, which is in the shape of -CH (CH 🥰) -2; the methyl group is -CH 🥰. The carbonyl group is a carbon-oxygen double bond structure and is located at the 4th position of the imidazoline ring.
Overall, the chemical structure of 2- (5-isopropyl-5-methyl-4-oxo-2-imidazoline-2-yl) -3-quinoline carboxylic acid is based on the quinoline ring, with a carboxyl group at the 3rd position and a specific imidazoline derivative at the 2nd position. The imidazoline ring contains isopropyl and methyl at the 5th position and carbonyl at the 4th position. Its structure is complex, and its parts are connected to each other to form a unique chemical structure.

This is a 2 - (5 - isopropyl - 5 - methyl - 4 - oxo - 2 - imidazoline - 2 - yl) - 3 - quinoline carboxylic acid. Its physical properties are as follows:
This compound is usually in a solid state. As for its melting point, different preparation methods and purity or cause it to vary, and it generally melts within a specific temperature range. In terms of solubility, it dissolves very little in water, and the hydrophobic part of its molecular structure accounts for a large proportion. However, in some organic solvents, such as dimethyl sulfoxide (DMSO), N, N-dimethylformamide (DMF), it exhibits good solubility, because these organic solvents can form specific intermolecular interactions with the compound, such as hydrogen bonds or van der Waals forces, which can help it dissolve.
Looking at its appearance, it is mostly white to off-white powder, and this color is related to the morphology, the aggregation state of the molecule and the crystal structure. In terms of stability, under normal environmental conditions, if light, hot topics and contact with active substances such as strong oxidants and strong bases are avoided, the compound can remain stable for a certain period of time. However, in case of high temperature, the chemical bonds in the molecule may break or rearrange, causing their decomposition. And in the strong acid and alkali environment, because the molecular structure contains reactive groups, such as carboxyl groups and imidazoline rings, chemical reactions are prone to occur, resulting in structural changes.

2-%285-Isopropyl-5-methyl-4-oxo-2-imidazolin-2-yl%29-3-quinolinecarboxylic + acid is 2 - (5 - isopropyl - 5 - methyl - 4 - oxo - 2 - imidazoline - 2 - yl) - 3 - quinoline carboxylic acid, which has a wide range of uses.
In the field of medicine, it may have significant pharmacological activity. Or it can be used as a lead compound for drug developers to explore in depth. After structural modification and optimization, it is expected to create specific drugs for specific diseases. For example, or for some inflammation-related diseases, with its special chemical structure, it precisely binds to inflammation-related targets in the body, thereby regulating the inflammatory response signaling pathway and achieving anti-inflammatory effect. Or it shows potential in tumor treatment, inhibiting tumor cell proliferation and inducing apoptosis by interfering with specific metabolic pathways or signal transduction of tumor cells.
In the field of chemical synthesis, it is a key organic synthesis intermediate. Because its structure contains a variety of active functional groups, it can participate in many organic reactions. It can be cleverly spliced with other organic molecules through reactions such as nucleophilic substitution and electrophilic addition to construct compounds with more complex and diverse structures, opening up new directions for organic synthetic chemistry and helping scientists create organic materials with novel structures and properties.
In the field of agriculture, through rational design and modification, new pesticides may be developed. Or it can have an efficient control effect on specific crop pests and diseases, and by virtue of its unique chemical properties, it can interfere with the physiological process of pests and diseases, achieve green and efficient prevention and control, and ensure crop yield and quality.

To prepare 2- (5-isopropyl-5-methyl-4-oxo-2-imidazoline-2-yl) -3-quinoline carboxylic acid, there are various methods. The common method is to take the appropriate quinoline derivative first, and the imidazoline compound containing a specific substituent, under suitable reaction conditions, so that the condensation reaction of the two occurs. During the reaction, the solvent needs to be carefully selected, such as the polar organic solvent, which can help the reactants to miscible and promote the reaction. And the reaction temperature also needs to be precisely adjusted, generally in the range of mild to medium temperature, to prevent side reactions from clumping. < Br >
Alternatively, the imidazoline structure can be constructed first, and then connected to the quinoline skeleton through a series of reactions. The choice of starting materials is crucial, and its activity and availability need to be considered. When preparing imidazoline parts, the corresponding amines and ketones can be obtained by cyclization.
Furthermore, the use of catalysts in the reaction process cannot be ignored. The selection of appropriate acid-base catalysts can effectively increase the reaction rate and advance the reaction in the direction of generating the target product. However, the amount of catalyst also needs to be strictly controlled. Too much or too little may affect the efficiency of the reaction and the purity of the product. After the reaction is completed, it needs to be separated and purified to obtain pure 2- (5-isopropyl-5-methyl-4-oxo-2-imidazoline-2-yl) -3 -quinoline carboxylic acid. This is the approximate path for synthesizing the compound. In actual operation, the reaction conditions and steps need to be flexibly adjusted according to the specific situation.

2-%285-Isopropyl-5-methyl-4-oxo-2-imidazolin-2-yl%29-3-quinolinecarboxylic acid is 2- (5-isopropyl-5-methyl-4-oxo-2-imidazoline-2-yl) -3-quinoline carboxylic acid. This compound has considerable market prospects.
Looking at today's pharmaceutical and chemical industries, there is a great demand for the exploration and application of new compounds. This compound has a unique structure and may have potential value in the field of drug research and development. The quinoline carboxylic acid part of its structure is common in many molecules with biological activity, or it can endow the compound with specific pharmacological activities, such as antibacterial, anti-inflammatory, and anti-tumor effects. As far as antibacterial is concerned, the problem of drug-resistant bacteria is severe today, and the research and development of new antibacterial compounds is a top priority, and this compound may become a potential candidate.
In the field of pesticides, it also has potential. With the gradual entry of the concept of green environmental protection, the development of high-efficiency, low-toxicity and environmentally friendly pesticides is the trend. The special structure of this compound may make it have insecticidal, bactericidal or weeding activities, and may meet the current stringent requirements for pesticides.
Furthermore, in the field of chemical synthesis, this compound may be used as a key intermediate. With its unique structure, chemically modified and transformed, a series of high-value-added compounds can be prepared, expanding the variety of chemical products and enhancing industrial economic benefits.
However, its marketing activities also pose challenges. To use it for drugs or pesticides, it needs to undergo rigorous safety and efficacy evaluation, which is time-consuming, laborious and expensive. And the market competition is fierce, and similar or alternative products have occupied a certain share. To stand out, it is necessary to highlight unique advantages.