1h Benzimidazole 5 Carboxamide 7 4s 5 7 Difluoro 3 4 Dihydro 2h 1 Benzopyran 4 Yl Oxy N N 2 Trimethyl
Quinoline Thiophene Imidazole Thiazole
1H-Benzimidazole-5-carboxamide, 7-[[(4S)-5,7-difluoro-3,4-dihydro-2H-1-benzopyran-4-yl]oxy]-N,N,2-trimethyl-
Chemical Formula C23H22F2N4O3
Molecular Weight 442.45 g/mol
FAQ

What is the chemical structure of 1H-benzimidazole-5-formamide, 7- [[ (4S) -5,7-difluoro-3,4-dihydro-2H-1-benzopyran-4-yl] oxy] -N, N, 2-trimethyl-?

This is a problem of structural description of organic compounds. In the analytical way of modern chemistry, the translation is as follows: the compound contains 1 hydrogen positive ion (1H < unk >), the main body is naphthalene and pyridine structure, and there is a methoxy group at the number 5 position (because "methyl ether" corresponds to methoxy group). There is a specific configuration fragment at the number 7 position, that is, (4S) -5,7-diene-3,4-dihydroxy-2H-1-naphthalene-pyridine-4-yl, this fragment has a hydroxyl group, and there is also an N, N, 2-trimethyl group structure in the molecule.

Answer in the simple style of "Tiangong Kaiwu": Looking at the question of this chemical structure, this compound first has a positive ion of hydrogen, such as Xingyao in its structure. Its main body is in the shape of a juxtaposed naphthalene and pyridine, which seems to have a unique structure. At its fifth position, there is a methoxy group connected, just like a branch born in the trunk. At position 7, there is a specific fragment with a (4S) configuration, containing diene and dihydroxyl groups, and a naphthalene and pyridine group with hydroxyl groups. In addition, see the structure of N, N, 2-trimethyl group, which is like the addition of a pavilion. All of these, interconnected, co-constitute the unique morphology of this compound, and each part is interdependent, forming a self-contained pattern in the microscopic world of chemistry, revealing its unique chemical properties and mysteries.

What are the physical properties of 1H-benzimidazole-5-formamide, 7- [[ (4S) -5,7-difluoro-3,4-dihydro-2H-1-benzopyran-4-yl] oxy] -N, N, 2-trimethyl-?

The compound is called (4S) -5,7-diene-3,4-dihydroxy-2H-1-naphthopyran-4-yloxy] -N, N, 2-trimethyl.

However, there is no exact data on its physical properties. Generally speaking, the physical properties of such organic compounds are closely related to the molecular structure. From a structural perspective, they contain naphthopyran structures, which often have a certain conjugate system, or give the compound specific optical properties, such as fluorescence under specific wavelengths of light. < Br >
In addition, it contains multiple hydroxy groups and methyl groups. Hydroxy groups can cause hydrogen bonds to form between molecules, which affects the boiling point and melting point of compounds. The force of hydrogen bonds can enhance the interaction between molecules, causing the boiling point to rise. Methyl groups are alkyl and have certain hydrophobicity, or affect the solubility of the compound in different solvents. Generally speaking, compounds containing more methyl groups have good solubility in organic solvents such as ethanol and ether, but limited solubility in water.

And because the compound has a complex structure or has a chiral center, (4S) indicates its specific three-dimensional configuration, chirality or its unique performance in optical rotation, which can cause polarized light to rotate. However, in order to know its physical properties, it is necessary to accurately determine its physical properties through experiments, such as using a melting point meter to measure the melting point, a boiling point meter to measure the boiling point, and a polarimeter to measure the optical rotation.

What are the chemical properties of 1H-benzimidazole-5-formamide, 7- [[ (4S) -5,7-difluoro-3,4-dihydro-2H-1-benzopyran-4-yl] oxy] -N, N, 2-trimethyl-?

This is an organic compound whose structure is quite complex. The compound has the following chemical properties:

First, its molecular structure contains a specific ring system, such as benzopyran structure, which endows it with certain stability and unique spatial configuration. Such ring systems can be used as reaction check points in chemical reactions, participating in electrophilic substitution, nucleophilic substitution and other reactions. For example, the benzene ring part can be alkylated with halogenated hydrocarbons under the catalysis of Lewis acid, and alkyl groups are introduced into the benzene ring.

Second, the hydroxyl and carbonyl groups contained in the molecule significantly affect its chemical activity. Hydroxyl groups can participate in esterification reactions and form ester compounds with carboxylic acids under acid catalysis; carbonyl groups are prone to nucleophilic addition reactions, such as reacting with Grignard reagents to generate alcohols.

Third, due to the presence of multiple unsaturated bonds in the molecule, it has a certain conjugate system. The conjugate system can enhance the degree of electron delocalization of the molecule, which in turn affects its physical and chemical properties. The compound may exhibit certain optical activities and have unique properties in photochemical reactions, such as absorbing light of specific wavelengths, initiating electron transitions within the molecule, and then photoisomerization.

Fourth, the nitrogen atom and alkyl group in the molecule also affect its chemical properties. Nitrogen atoms can provide lone pairs of electrons to participate in coordination reactions and form complexes; while the electronic effect of alkyl groups affects the activity of adjacent functional groups, and long-chain alkyl groups also affect the solubility and fat solubility of compounds.

In summary, this compound has a variety of functional groups and special structures due to its complex structure, which makes it have a variety of chemical properties and may have potential application value in organic synthesis, medicinal chemistry and other fields.

1H-benzimidazole-5-formamide, 7- [[ (4S) -5,7-difluoro-3,4-dihydro-2H-1-benzopyran-4-yl] oxy] -N, N, 2-trimethyl-In what fields is it used?

I look at this chemical formula, which is quite complicated. This "1H + -Bupleurum pyridine-5-methyl ether, 7- [ (4S) -5,7-diene-3,4-diol-2H-1-Bupleurum pyran-4-yl] oxy-N, N, 2-trimethyl" material may be of great use in the field of medicine.

In the field of pharmaceutical research and development, such compounds may have unique pharmacological activities. For example, Bupleurum is a traditional Chinese medicine, with the effect of reconciling the surface and the inside, soothing the liver and raising yang. This compound combines Bupleurum-related structures with pyridine, etc., and may be able to derive new drugs for the treatment of various diseases, such as poor gas regulation and visceral disharmony.

In the field of organic synthesis, the synthesis process must be challenging. It is necessary to precisely design the reaction path and control the reaction conditions to accurately construct this complex structure. Chemists may use this to expand the boundaries of synthetic chemistry, develop novel synthetic methods and strategies, and lay the foundation for the preparation of more complex compounds.

In the field of biological activity research, it is possible to explore its interaction with targets in organisms. By leveraging modern biotechnology to clarify its mechanism of action, new biological activities may be discovered, providing an opportunity for innovative drug development and opening up new ideas for the treatment of difficult diseases.

What is the preparation method of 1H-benzimidazole-5-formamide, 7- [[ (4S) -5,7-difluoro-3,4-dihydro-2H-1-benzopyran-4-yl] oxy] -N, N, 2-trimethyl-?

To prepare this substance, the method is as follows: First take an appropriate amount of (4S) -5,7-diene-3,4-dihydroxy-2H-1-naphthopyran-4-yloxy and place it in a suitable container. This is the key starting material and needs to be taken with caution to ensure its quality is pure.

Then, add an appropriate amount of N, N, 2-trimethylamino to it. When adding this reagent, control the speed and amount, drop it slowly, and pay close attention to changes in the reaction system to prevent overreaction.

As for methyl ether naphthaldehyde, it is also an important reactant. Add to the reaction system in the appropriate proportion and interact with the previously added raw materials and reagents. This step requires strict control of the reaction temperature and time to ensure that the reaction can proceed in the desired direction.

During the entire preparation process, the control of the reaction environment is crucial. The temperature should be maintained within a certain precise range, or controlled by specific heating and cooling devices. And the reaction system needs to be kept clean to avoid impurities from mixing and interfering with the reaction process.

At the same time, the process of the reaction needs to be closely monitored. By means such as chromatographic analysis, the degree of reaction can be known in real time, so that appropriate measures can be taken at the appropriate time to ensure that the purity and yield of the final product can reach the expected standard. Only in this way can we successfully obtain what we need.