Chemical Formula | C24H32FN3O6 |
Molecular Weight | 477.527 g/mol |
Physical State At Room Temperature | Solid |
Solubility In Water | Low (organic compound with hydrophobic groups) |
Solubility In Organic Solvents | Soluble in common organic solvents like dichloromethane, chloroform |
Logp | Positive value indicating lipophilic nature due to fluorobenzyl and pivalate groups |
Chemical Formula | C24H31FN4O5 |
Molecular Weight | 474.527 g/mol |
Appearance | Solid (predicted) |
Boiling Point | 620.3±55.0 °C at 760 mmHg (predicted) |
Melting Point | 157 - 160 °C |
Logp | 2.85 (predicted) |
Pka | 12.58±0.70 (predicted) |
Solubility | Soluble in organic solvents like DMSO |
Density | 1.234±0.06 g/cm3 (predicted) |
Refractive Index | 1.557 (predicted) |
2- (2-aminopropan-2-yl) -4- [ (4-fluorobenzyl) carbamoyl] -1-methyl-6-oxo-1, what is the chemical structure of 6-dihydropyrimidin-5-yl pivalate
This is the name of an organic compound. To clarify its chemical structure, the following steps are required.
First analysis "2- (2-aminopropyl-2-yl) -4- [ (4-fluorobenzyl) aminoformyl] -1-methyl-6-oxo-1,6-dihydropyrimidine-5-ylneovalerate". "Pyrimidine" is a six-membered nitrogen-containing heterocyclic parent nucleus with two nitrogen atoms in an intermediate position. In the 1,6-dihydropyrimidine-6-ketone structure, there is a methyl group in the first position, which replaces the hydrogen atom; the 4-fluorobenzyl group is connected to the amino group, that is, the 4-fluorobenzyl group is connected to the pyrimidine ring through the carbamyl group, and the 4-fluorobenzyl group is substituted with a fluorine atom on the benzene ring and is connected to the methylene group, which is then connected to the amino group; the 2-aminopropyl-2-group is connected to the 2-position nitrogen atom of the isopropyl group, which replaces the hydrogen atom to form the amino group. The fifth position is connected to the neovalerate. Neovaleric acid removes a carboxyl hydrogen from pentanoic acid and is connected to the fifth position of the pyrimidine ring by ester bond.
Its overall chemical structure is based on 1,6-dihydropyrimidine-6-one as the core, and multiple substituents are connected to the pyrimidine ring at specific positions, and each substituent gives the compound unique chemical and physical properties. After this analysis, the chemical structure of this compound is clearly presented.
2- (2-aminopropan-2-yl) -4- [ (4-fluorobenzyl) carbamoyl] -1-methyl-6-oxo-1, what are the main uses of 6-dihydropyrimidin-5-yl pivalate
2-%282-aminopropan-2-yl%29-4-%5B%284-fluorobenzyl%29carbamoyl%5D-1-methyl-6-oxo-1%2C6-dihydropyrimidin-5-yl+pivalate, this is the name of an organic compound, which has a complex structure and is composed of many specific groups. In the field of practical applications, this compound is often found in the corner of medicinal chemistry.
In the field of pharmaceuticals, it may be a key active ingredient. When developing new drugs, it can target specific disease targets. For example, some diseases arise from abnormal metabolism or disorders of signaling pathways in specific cells in the body. By combining with related targets, this compound may be able to correct these abnormalities, so as to achieve the purpose of treating diseases.
In the process of scientific research and exploration, it may also be an important research object. Scientists can conduct various experiments on it, such as the exploration of chemical reaction mechanisms, the study of interactions with biological macromolecules, etc., to gain in-depth insights into the laws of organic chemistry and the mysteries of life science. For example, by studying its binding mode with proteins, the mechanism of molecular recognition in organisms can be clarified, laying the foundation for subsequent more targeted drug design and development.
In addition, in the field of organic synthesis, it may be a key intermediate for the synthesis of other more complex compounds. Chemists can use ingenious reaction design as a basis to further introduce other functional groups to construct compounds with novel structures and unique functions, thereby expanding the variety and application range of organic compounds.
2- (2-aminopropan-2-yl) -4- [ (4-fluorobenzyl) carbamoyl] -1-methyl-6-oxo-1, what is the production method of 6-dihydropyrimidin-5-yl pivalate
To prepare 2 - (2 - aminopropyl - 2 - yl) - 4 - [ (4 - fluorobenzyl) carbamoyl] - 1 - methyl - 6 - oxo - 1,6 - dihydropyrimidine - 5 - ylneoprene, the method is as follows:
Take an appropriate amount of 1 - methyl - 4 - [ (4 - fluorobenzyl) carbamoyl] - 6 - oxo - 1,6 - dihydropyrimidine - 2,5 - dicarboxylic acid anhydride and place it in a clean reactor , dissolve in an appropriate amount of organic solvent, such as dichloromethane or N, N-dimethylformamide, stir well to form a homogeneous solution.
Take another 2-amino-2-methylpropanol and slowly add it dropwise to the above reaction kettle to control the dropwise rate and do not make the reaction too violent. At the same time, add an appropriate amount of organic base, such as triethylamine or pyridine, to the reaction system to promote the reaction. The reaction temperature is maintained in a suitable range, usually between 20 ° C and 40 ° C. The reaction lasts for several hours, during which time sampling and detection are carried out. The reaction progress is monitored by thin layer chromatography or high performance liquid chromatography until the raw material 1-methyl-4- [ (4-fluorobenzyl) carbamoyl] -6-oxo-1,6-dihydropyrimidine-2,5-dicarboxylic acid anhydride is mostly converted.
When the reaction reaches the desired level, pour the reaction solution into an appropriate amount of water, extract it with an organic solvent, and collect the organic phase. The organic phase is dried with anhydrous sodium sulfate, filtered to remove the desiccant, and the organic solvent is removed by reduced pressure distillation to obtain a crude product.
The crude product was further separated and purified by column chromatography. Silica gel was used as the stationary phase, and a mixture of petroleum ether and ethyl acetate in an appropriate proportion was used as the eluent. The eluent containing the target product was collected and concentrated under reduced pressure to obtain a pure 2- (2-aminopropyl-2-yl) -4- [ (4-fluorobenzyl) carbamoyl] -1-methyl-6-oxo-1,6-dihydropyrimidine-5-ylneoprene. During operation, it is necessary to pay attention to safety. Organic solvents are more flammable and volatile, so they should be avoided from open flames and carried out with good ventilation.
2- (2-aminopropan-2-yl) -4- [ (4-fluorobenzyl) carbamoyl] -1-methyl-6-oxo-1, what is the safety of 6-dihydropyrimidin-5-yl pivalate
2-%282-aminopropan-2-yl%29-4-%5B%284-fluorobenzyl%29carbamoyl%5D-1-methyl-6-oxo-1%2C6-dihydropyrimidin-5-yl + pivalate, it is also a chemical substance. Its safety is involved, which cannot be hidden in one word, and needs to be tested at multiple ends.
First, its chemical production. The production of this compound, its physical and chemical properties, also affect its characterization in different environments. If the production contains active radicals, or is easy to react to other substances, it will be stored, damaged, or biodegraded, endangering safety.
Its toxicological characteristics are observed for the first time. The study of the substance and the phase can be used to know the impact of its biological effects. Such as oral, skin, inhalation, etc., its acute toxicity is determined to determine the risk of short-term and high-level exposure. Chronic toxicity studies should not be ignored. It can be seen that under low-level exposure in the early stage, various strains, such as liver, liver, and other diseases, are in the shadow.
Furthermore, consider its environmental safety. If this substance is in the environment, it is necessary to know its degradation characteristics. Whether it can be degraded by microorganisms, photolysis, etc. in the natural environment, or whether it is tired in the period, the biological system needs to be considered. The toxicity of aquatic organisms and biological organisms is also essential for environmental safety assessment.
In the process of production, the operation of raw materials, middle materials, and most substances, if it is appropriate to prevent, workers may be exposed. It is also necessary to ensure that it is used according to the standard, such as for the purpose of transportation and transportation, so as to avoid harm to the user and the surrounding environment.
The safety of 2-%282-aminopropan-2-yl%29-4-%5B%284-fluorobenzyl%29carbamoyl%5D-1-methyl-6-oxo-1%2C6-dihydropyrimidin-5-yl + pivalate requires comprehensive and comprehensive research, chemical, toxicological, environmental, and engineering analysis, etc., in order to ensure the safety of its use in various domains.
2- (2-aminopropan-2-yl) -4- [ (4-fluorobenzyl) carbamoyl] -1-methyl-6-oxo-1, what is the market outlook for 6-dihydropyrimidin-5-yl pivalate
There is a product called 2- (2-aminopropyl-2-yl) -4- [ (4-fluorobenzyl) carbamoyl] -1-methyl-6-oxo-1,6-dihydropyrimidine-5-ylneoprene. The market prospect of this product is really related to many factors, so let me tell them one by one.
From the perspective of the medical field, if it has unique pharmacological activity, can target specific disease targets with precise action, significant curative effect and mild side effects, the future is bright. If there are many difficult diseases at present, if this product can be used as an innovative treatment drug, the medical community will flock to it, and the market demand may be like water from a river, rolling in. However, the competition in the pharmaceutical market is fierce, and the research and development of new drugs needs to go through many barriers, from laboratory research to clinical trials, which takes a long time and requires huge investment. If the competing product has already entered the market and occupied the market share, it will be difficult for this product to stand out.
In the chemical industry, as a fine chemical product, if the production process is advanced, the cost is controllable, and the quality is stable, it may be able to find a place in the relevant chemical industry chain. It can be used to synthesize other high-value-added products and expand the scope of application. However, the changing chemical market, fluctuations in raw material prices, and tightening environmental protection policies are all obstacles to its development. If such variables cannot be dealt with, production or hindered, the road to the market will also be bumpy.
Furthermore, looking at the economic environment, the economy is prosperous, the market is full of vitality, and the demand for new compounds may increase, which may welcome development opportunities; the economy is sluggish, investment in various industries is tightened, R & D, production and marketing activities are constrained, and its market expansion is difficult.
To sum up, the market prospects, opportunities and challenges of 2- (2-aminopropyl-2-yl) -4- [ (4-fluorobenzyl) carbamoyl] -1-methyl-6-oxo-1,6-dihydropyrimidine-5-ylpivalate coexist. Only by grasping the development pulse of the pharmaceutical and chemical industries and responding to various variables can we seek development in the market and open up a world.