N-(2-(4-(amino sulfonyl) phenyl)ethyl)-3-ethyl-4-methyl-2-oxo-2,5-dihydro-1H-pyrrole-1-carboxamide

This is the name of an organic compound. According to this name, its chemical structure is similar to the ancient alchemy method, which requires layer-by-layer analysis. This name is "N- (2- (4- (aminosulfonyl) phenyl) ethyl) -3-ethyl-4-methyl-2-oxo-2,5-dihydro-1H-pyrrole-1-formamide", and its core structure is 1H-pyrrole-1-formamide. At the position of 2,5-dihydro, the 2-oxo generation has already formed a bond, which is the key skeleton.
Looking at its N-substituent, it is "2- (4- (aminosulfonyl) phenyl) ethyl", just like adding a long chain to the skeleton. In this long chain, ethyl is connected to the 2-position of phenyl, and the 4-position of phenyl is connected to the aminosulfonyl group, which has a delicate structure, just like the ancient tenon-and-mortise fit. Looking at the pyrrole ring again, the 3-position is connected to ethyl, and the 4-position is connected to methyl, and the distribution of each substituent is orderly, just like the stars are listed in the sky.
The chemical structure of this compound, after being disassembled and analyzed in this way, is like an exquisite ancient painting, unfolding before your eyes. Its various parts are connected to form a unique spatial structure, which shows its unique charm in the world of organic chemistry, just like the mysterious elixir formula recorded in ancient secret books. The combination of various ingredients results in a wonderful structure.

This is an organic compound, and its physical properties are quite important. Its appearance is often white to light yellow solid powder, which shows a specific aggregation state due to the arrangement and interaction of atoms in the molecular structure. The melting point is within a certain range, which is closely related to the intermolecular forces. There are van der Waals forces, hydrogen bonds, etc., between molecules, and specific energy is required to overcome these forces to cause molecules to break free from the lattice and melt. The boiling point also has a corresponding value. When enough energy is provided, molecules can overcome the intermolecular forces and transform from liquid to gaseous.
In terms of solubility, organic solvents such as dichloromethane, N, N-dimethylformamide have a certain solubility, because their molecular structure is partially organic solvent-friendly. However, the solubility in water is relatively low. Due to the large proportion of the hydrophobic part of the molecule as a whole, it is difficult to form an effective interaction between water molecules and the molecules of the compound. Density is also one of its physical properties, which is determined by the molecular mass and the degree of molecular accumulation. The density of the compound is moderate, reflecting the mass distribution of molecules in a unit volume. In addition, its stability cannot be ignored. It is relatively stable under normal conditions. In case of extreme conditions such as high temperature, strong acid, and strong base, the molecular structure may change, resulting in changes in physical properties. These are all important physical properties of the compound and are extremely critical in research and application.

This is an organic compound called N- (2- (4- (aminosulfonyl) phenyl) ethyl) -3-ethyl-4-methyl-2-oxo-2,5-dihydro-1H-pyrrole-1-formamide. In modern times, such compounds are mostly used in the field of pharmaceutical chemistry, and their primary function is to serve as a key intermediate for drug development.
Guanfu's way of pharmaceutical research and development, such compounds can be combined with other chemical substances through specific chemical reactions to construct drug molecules with specific biological activities. Due to its unique chemical structure, it can interact with specific targets in organisms, or regulate physiological processes, or intervene in the mechanism of disease occurrence and development, so it plays an indispensable role in the creation of new drugs.
For example, in some drug research for specific diseases, such as tumors, inflammation, etc., this compound or because of its structure and target compatibility, can be used as a starting material, through a series of fine chemical modifications and reactions, into potential therapeutic drugs with high-efficiency and low-toxicity properties. It is often relied on by researchers in the laboratory synthesis and pre-clinical research stages, and is an important cornerstone for exploring new therapeutic drugs.

There are various ways to synthesize N- (2- (4- (aminosulfonyl) phenyl) ethyl) -3-ethyl-4-methyl-2-oxo-2,5-dihydro-1H-pyrrole-1-formamide.
First, it can be prepared from a suitable starting material through a multi-step reaction. First, take the benzene derivative with the corresponding substituent and react it with a vinyl compound containing a specific functional group to form a carbon-carbon bond to obtain an intermediate containing a phenethyl structure. This step may require the selection of suitable catalysts and reaction conditions, such as the use of metal-catalyzed coupling reactions, to ensure the selectivity and yield of the reaction. < Br >
Then, the obtained intermediate is reacted with another pyrrole ring-containing precursor. This pyrrole ring precursor may need to be modified by specific functionalization in advance to enable smooth reaction with phenethyl intermediates to construct the core pyrrole-formamide structure of the target molecule. In this step of the reaction, attention may be paid to the stereochemistry and regioselectivity of the reaction to obtain the product with the correct configuration. During the
reaction process, the intermediates in each step need to be purified and characterized. They can be purified by column chromatography, recrystallization, etc., and characterized by nuclear magnetic resonance and mass spectrometry to confirm that the structure is correct. Finally, the purity and structure of the obtained product need to be strictly analyzed to ensure that the target N- (2- (4- (aminosulfonyl) phenyl) ethyl) -3-ethyl-4-methyl-2-oxo-2,5-dihydro-1H-pyrrole-1-formamide. The whole synthesis process requires fine regulation of the reaction conditions and attention to the connection and optimization of each step of the reaction to obtain this compound efficiently.

N - (2 - (4 - (aminosulfonyl) phenyl) ethyl) - 3 - ethyl - 4 - methyl - 2 - oxo - 2,5 - dihydro - 1H - pyrrole - 1 - formamide, this compound is worth exploring in today's market prospects.
Looking at the current fields of medicine and chemical industry, the demand for new organic compounds is increasing. This compound has a unique molecular structure, or it has emerged at the end of drug development. Its structure contains specific groups such as pyrrole ring and sulfonylamino group, which often endow the compound with diverse biological activities. In the field of drug creation, or by virtue of its structural properties, it can be combined with specific biological targets to exhibit pharmacological effects such as antibacterial, anti-inflammatory, and anti-tumor.
Furthermore, in the field of materials science, compounds with such structures may be used as building blocks of functional materials. After rational design and modification, materials may be endowed with special electrical, optical, or mechanical properties, such as for the preparation of new optoelectronic materials, or to improve the stability and functionality of materials to meet the needs of electronic and optical device manufacturing industries.
However, its market prospects also face various challenges. The process or complexity of synthesizing this compound, cost control is the key. In order to achieve large-scale production and wide application, it is necessary to optimize the synthesis route, increase the yield and reduce the cost. And before it is put into the market, it needs to undergo strict safety and effectiveness evaluation, especially in the field of medicine, it needs to follow strict regulations and standards.
In summary, although N - (2 - (4 - (aminosulfonyl) phenyl) ethyl) - 3 - ethyl - 4 - methyl - 2 - oxo - 2,5 - dihydro - 1H - pyrrole - 1 - formamide has a promising market, it is necessary to overcome the problems of synthesis and evaluation in order to gain a place in the market and exert its due value.