What is the chemical structure of 1- (2,6-difluorobenzyl) -5- ((dimethylamino) methyl) -3- (6-methoxypyridazine-3-yl) -6- (4-nitrophenyl) thiopheno [2,3-d] pyrimidine-2,4 (1H, 3H) -dione?

The chemical structure of this compound can be described in detail.

The first word is 1- (2,6-diethylamino), which is at position 1 of the main structure, with 2,6-diethylamino groups. For diethylamino, the two hydrogen atoms of the amino group are substituted by ethyl, and its structure is -N (C ² H) -2.

times and 5- ((dimethoxy) methyl). At position 5, there are dimethoxy-substituted methyl groups, namely -CH (OCH 🥰) -2. This structure imparts specific chemical properties and steric resistance to the compound.

In addition, 3- (6-methoxypyridine-3-yl), the position 3 is connected to 6-methoxypyridine-3-yl. The pyridine ring is a nitrogen-containing six-membered heterocycle, and the 6-methoxypyridine-3-yl is connected to the main body at position 3 of the pyridine ring, and there is a methoxy-OCH at position 6.

There is also 6- (4-fluorobenzyl) imidazolo [2,3-d] pyrimidine-2,4 (1H, 3H) -dione, which is connected to 4-fluorobenzyl at position 6, and 4-fluorobenzyl is benzyl. The benzene ring of benzyl at position 4 has a fluorine atom substitution, that is, -CH ² - C H - F. The imidazolo [2,3-d] pyrimidine-2,4 (1H, 3H) -dione part, the imidazolo pyrimidine ring is a thick heterocyclic structure, with carbonyl groups at the 2,4 positions and hydrogen atoms at the 1,3 positions, respectively. This structure is the core part of the compound and has a great impact on its biological activity and other properties.

In summary, the chemical structure of the compound is formed by connecting the above parts, and each group interacts, giving it unique chemical and physical properties.

What are the physical properties of 1- (2,6-difluorobenzyl) -5- ((dimethylamino) methyl) -3- (6-methoxypyridazine-3-yl) -6- (4-nitrophenyl) thiopheno [2,3-d] pyrimidine-2,4 (1H, 3H) -dione

1-%282%2C6-%E4%BA%8C%E6%B0%9F%E8%8B%84%E5%9F%BA%29-5-%28%28%E4%BA%8C%E7%94%B2%E6%B0%A7%E5%9F%BA%29%E7%94%B2%E5%9F%BA%29-3-%286-%E7%94%B2%E6%B0%A7%E5%9F%BA%E5%93%92%E5%97%AA-3-%E5%9F%BA%29-6-%284-%E7%A1%9D%E5%9F%BA%E8%8B%AF%E5%9F%BA%29%E5%99%BB%E5%90%A9%E5%B9%B6%5B2%2C3-d%5D%E5%98%A7%E5%95%B6-2%2C4%281H%2C3H%29-%E4%BA%8C%E9%85%AE%E7%9A%84%E7%89%A9%E7%90%86%E6%80%A7%E8%B4%A8%E4%B8%8E%E5%85%B6%E5%85%83%E7%B4%A0%E7%BB%84%E6%88%90%E5%8F%8A%E7%BB%93%E6%9E%84%E7%9B%B8%E5%85%B3. The following are the characteristics:

This compound has a specific molecular structure and is composed of a combination of various functional groups. Among them, 2,6-diethylamino, dimethylamino and other groups endow it with certain electronic properties. In terms of physical properties, due to the influence of intermolecular forces, or with specific melting points. Nitrogen-containing functional groups can make it soluble in a suitable solvent, but the specific solubility depends on the polarity of the solvent and other factors.

From the perspective of polarity, the polarity of different functional groups is different, and the polarity of the whole molecule is also affected by its spatial arrangement. If the molecular structure is symmetric, the polarity is weak; conversely, if the structure is asymmetric, the polarity is strong. This polarity has a significant impact on its behavior in different media. For example, in chromatographic separation, different polarities can cause different retention times.

In terms of density, it is related to the relative molecular weight and the degree of molecular accumulation. Generally speaking, those with large relative molecular weight and tight molecular accumulation have higher densities.

In addition, some hydrogen atoms in this compound (such as hydrogen at 2,4 (1H, 3H) -dione), due to different chemical environments, will have specific chemical shifts in the hydrogen NMR spectrum, which can provide important information for structure identification. Its physical properties may vary with external conditions (e.g. temperature, pressure), such as temperature increase, molecular thermal motion intensifies, melting and boiling points may be affected, and solubility may also change.

What is the synthesis method of 1- (2,6-difluorobenzyl) -5- ((dimethylamino) methyl) -3- (6-methoxypyridazine-3-yl) -6- (4-nitrophenyl) thiopheno [2,3-d] pyrimidine-2,4 (1H, 3H) -dione?

To prepare 1- (2,6-diethylamino) -5- ((dimethylamino) methyl) -3- (6-methoxypyridine-3-yl) -6- (4-fluorobenzyl) quinazolino [2,3-d] pyrimidine-2,4 (1H, 3H) -dione, the following ancient method can be used.

Take an appropriate reaction vessel, wash and dry to remove water vapor impurities. Pour the raw material containing 2,6-diethylamino carefully into it according to accurate stoichiometry. This raw material needs to be purified in advance to maintain purity before the reaction can be smooth.

The 5- ((dimethylamino) methyl) related reactants are injected for the second time. When operating, pay attention to their properties. If there is a appearance of deliquescence or deterioration, it should not be used. After the injection, stir slowly to make the material initially mixed evenly.

Then, add 3- (6-methoxypyridine-3-yl) reagent. The addition process needs to control the rate to prevent overreaction. At this stage, the temperature and pressure can be adjusted appropriately according to the characteristics of the reaction system. Generally speaking, maintaining a moderate temperature can make the reaction proceed in the desired direction and increase the yield. For example, the temperature can be controlled in a specific range, such as between [X] ° C and [X] ° C, and the pressure is stable at [X] kPa.

Then introduce some raw materials of 6- (4-fluorobenzyl) quinazolino [2,3-d] pyrimidine-2,4 (1H, 3H) -dione. This step needs to be handled with caution. Because of its high reactivity, a little carelessness can easily cause side reactions to occur. After adding, continue to stir to observe the phenomenon of color change and state change of the reaction system to judge the reaction process. < Br >
During the reaction process, the degree of reaction needs to be monitored in real time by means such as thin layer chromatography (TLC). When the reaction is almost complete, that is, the expected reaction endpoint is reached, and the reaction product can be post-processed. First extract with an appropriate solvent to separate the organic phase, and then purify the product by distillation, recrystallization, etc., to remove impurities, and finally obtain a pure target product. The whole process requires strict compliance with operating procedures and precise control of various reaction parameters to obtain high-quality products.

What are the application fields of 1- (2,6-difluorobenzyl) -5- ((dimethylamino) methyl) -3- (6-methoxypyridazine-3-yl) -6- (4-nitrophenyl) thiopheno [2,3-d] pyrimidine-2,4 (1H, 3H) -dione?

In the field of chemistry in our country, 1 - (2,6 - diethylamino) - 5 - ((dimethylamino) methyl) - 3 - (6 - methoxypyridine - 3 - yl) - 6 - (4 - piperidinylbenzyl) imidazolo [2,3 - d] pyrimidine - 2,4 (1H, 3H) -dione has a wide range of application fields.

In the field of pharmaceutical research and development, this compound may have unique pharmacological activity. Due to the many special groups contained in its structure, such as diethylamino, methoxypyridyl, etc., it may interact with specific biological targets. Because of the spatial structure and electronic properties of these groups, they can conform to the activity check point of biological macromolecules, and then regulate the physiological and biochemical processes in vivo. Therefore, it may play a key role in the exploration of new drugs, such as anti-cardiovascular drugs, anti-tumor drugs, etc. It can be used as a lead compound. Pharmacists can use this as a basis to improve the efficacy of drugs, reduce toxic and side effects, and bring good news to patients through structural modification and optimization.

In the field of materials science, this compound may be used to prepare functional materials. Due to the complexity and particularity of its structure, or endowing materials with unique physical and chemical properties. For example, its intermolecular forces, optical properties, etc. may be changed by special groups. Or it can be used to prepare adsorbent materials with specific adsorption properties for the separation and purification of specific substances; or in the field of optical materials, due to the influence of its special structure on light absorption and emission, or it can prepare new optical sensors to achieve high sensitivity detection of specific substances.

In the field of organic synthetic chemistry, this compound is an important target molecule for organic synthesis. Its complex structure challenges the synthetic skills of chemists and motivates the development of new synthesis methods and strategies. With this goal, chemists can explore novel reaction pathways and develop efficient catalytic systems to advance organic synthesis chemistry. These new methods and strategies can not only be used in the synthesis of this compound, but also can be widely used in the construction of other complex organic molecules, expanding the boundaries of organic synthesis.

What is the market prospect of 1- (2,6-difluorobenzyl) -5- ((dimethylamino) methyl) -3- (6-methoxypyridazine-3-yl) -6- (4-nitrophenyl) thiopheno [2,3-d] pyrimidine-2,4 (1H, 3H) -dione?

Looking at this question, all the terms mentioned are related to chemistry, which seems to be seeking the prospect of chemical substances in the market. In the words of "Tiangong Kaiwu", it is as follows:

There is a substance today, which is called 1-%282%2C6-%E4%BA%8C%E6%B0%9F%E8%8B%84%E5%9F%BA%29-5-%28%28%E4%BA%8C%E7%94%B2%E6%B0%A7%E5%9F%BA%29%E7%94%B2%E5%9F%BA%29-3-%286-%E7%94%B2%E6%B0%A7%E5%9F%BA%E5%93%92%E5%97%AA-3-%E5%9F%BA%29-6-%284-%E7%A1%9D%E5%9F%BA%E8%8B%AF%E5%9F%BA%29%E5%99%BB%E5%90%A9%E5%B9%B6%5B2%2C3-d%5D%E5%98%A7%E5%95%B6-2%2C4%281H%2C3H%29-%E4%BA%8C%E9%85%AE. This substance has unique characteristics, its composition is exquisite, contains a variety of groups, and interacts to create its unique nature.

In today's market, the demand for chemical substances often depends on the rise and fall of each industry. If the characteristics of this substance are suitable for booming industries, such as medicine and materials, its prospects are considerable. The way of medicine is to seek accurate and effective ingredients. If this substance can be used as the key ingredient of medicine, or as the cornerstone of research and development of new drugs, with its unique structure, or can show novel curative effects, it will be valued by the pharmaceutical industry, and the market prospect should be broad.

As for the material industry, we continue to pursue new materials to meet the needs of construction, electronics and other industries. If this substance has outstanding performance in material characteristics, such as strength, stability, conductivity, etc., it will be favored by the material field, and the market will also be promising.

However, the market situation changes, and it is also necessary to observe the state of peer competition. If similar substances have flooded the market, or there are more superior substitutes, it may not be easy for this substance to gain a place in the market. It is necessary to study it carefully, explore its unique advantages, or improve the process and reduce its cost in order to gain an advantage in the market and have a bright future.