N 2 Chloro 6 Methylphenyl 2 6 Chloro 2 Methyl 4 Pyrimidinyl Amino 5 Thiazolecarboxamide
Quinoline Thiophene Imidazole Thiazole
n-(2-chloro-6-methylphenyl)-2-((6-chloro-2-methyl-4-pyrimidinyl)amino)-5-thiazolecarboxamide
Chemical Formula C16H13Cl2N5OS
Molecular Weight 392.27
Iupac Name N-(2-chloro-6-methylphenyl)-2-[(6-chloro-2-methylpyrimidin-4-yl)amino]thiazole-5-carboxamide
Appearance Solid (usually powder)
Physical State Solid at room temperature
Solubility Limited solubility in water, may be soluble in some organic solvents
Melting Point Typically has a defined melting point (specific value requires experimental determination)
Pka pKa values would depend on acidic/basic functional groups (specific values need experimental measurement)
Logp Indicates lipophilicity (specific value requires experimental determination)
FAQ

What is the chemical structure of the n- (2-chloro-6-methylphenyl) -2- ((6-chloro-2-methyl-4-pyrimidinyl) amino) -5-thiazolecarboxamide?

This is a rather complex organic compound named N- (2-chloro-6-methylphenyl) -2 - ((6-chloro-2-methyl-4-pyrimidinyl) amino) -5 -thiazolecarbonamide. To clarify its chemical structure, it is necessary to analyze it according to the organic chemistry nomenclature.

"N- (2-chloro-6-methylphenyl) ", this part indicates that the compound has a substituent, that is, a 2-chloro-6-methylphenyl group attached to the nitrogen atom (N). Phenyl is the benzene ring to remove the remaining group of a hydrogen atom, and 2-chloro-6-methyl indicates the substituted position of the chlorine atom and the methyl based on the benzene ring, which are in the carbon positions of No. 2 and No. 6, respectively.

"2- ((6-chloro-2-methyl-4-pyrimidinyl) amino) ", this section means that at the No. 2 position of the main chain of the compound, a 6-chloro-2-methyl-4-pyrimidinyl group is connected to the amino group. Pyrimidine is a six-membered heterocyclic compound containing two nitrogen atoms, and the 6-chloro-2-methyl-4-pyrimidinyl group indicates the substitution position of the chlorine atom and the methyl based on the pyrimidine ring.

"5-thiazole formamide" indicates that the main chain is a thiazole structure, and a formamide group is connected at position 5 of the thiazole ring. Thiazole is a five-membered heterocyclic ring containing sulfur and nitrogen atoms, and formamide is composed of carbonyl groups connected to amino groups.

In summary, the structure of this compound is composed of phenyl, pyrimidinyl, thiazole ring and corresponding substituents connected to each other. The structure is quite complex, and each part is combined according to specific rules to construct a unique chemical structure.

What are the main uses of n- (2-chloro-6-methylphenyl) -2- ((6-chloro-2-methyl-4-pyrimidinyl) amino) -5-thiazolecarboxamide?

N- (2-chloro-6-methylphenyl) - 2 - ((6-chloro-2-methyl-4-pyrimidinyl) amino) - 5-thiazolecarbonamide, an organic compound, has key uses in the current field of pharmaceutical and pesticide research and development.

In the field of pharmaceutical research and development, such compounds are mostly regarded as potential pharmaceutical active ingredients. Due to their unique structure, they may exhibit high affinity and selectivity for specific biological targets, thereby regulating related physiological processes in vivo. For example, it has been found that some thiazolecarbonamide derivatives with similar structures can effectively inhibit the proliferation of some tumor cells. This compound may interfere with the cell cycle process and induce tumor cell apoptosis by precisely acting on specific signaling pathway proteins in tumor cells, opening up new paths for the development of anti-cancer drugs. At the same time, in the field of inflammation-related disease treatment, such compounds may also regulate the release of inflammatory mediators, reduce inflammatory responses, and demonstrate potential therapeutic value.

In the field of pesticide research and development, this compound may have significant biological activity. Thiazolecarbonamide compounds often have inhibitory and killing effects on a variety of pests and pathogenic bacteria. Or because of their unique chemical structure, they can combine with specific receptors or enzymes in pests or pathogens, destroying their normal physiological functions. For example, it can interfere with the signal transduction of the insect nervous system, make the insect behavior disordered, unable to feed and reproduce normally; or inhibit the cell wall synthesis or energy metabolism process of pathogenic bacteria, inhibit the growth and spread of pathogenic bacteria, and provide a novel and efficient means for agricultural pest control.

In summary, N- (2-chloro-6-methylphenyl) -2- ((6-chloro-2-methyl-4-pyrimidinyl) amino) -5-thiazolecarbonamide has shown broad application prospects in the two fields of medicine and pesticides, and is expected to make important contributions to human health and agricultural production due to its unique chemical structure and potential biological activity.

What are the production processes of n- (2-chloro-6-methylphenyl) -2- ((6-chloro-2-methyl-4-pyrimidinyl) amino) -5-thiazolecarboxamide?

N- (2-chloro-6-methylphenyl) -2 - ((6-chloro-2-methyl-4-pyrimidinyl) amino) -5 -thiazolecarbonamide is a complex organic compound. The preparation process is quite delicate and requires specific steps and conditions.

The selection of starting materials is the key. 2-chloro-6-methylaniline, 6-chloro-2-methyl-4-pyrimidine amine and 5-thiazole formyl chloride are commonly used. It is necessary to ensure that the raw materials are pure and have few impurities in order to pave the way for subsequent reactions.

In the reaction process, shilling 2-chloro-6-methylaniline and 6-chloro-2-methyl-4-pyrimidine amine in a suitable solvent are catalyzed by a base, and nucleophilic substitution occurs at a suitable temperature. This step requires close monitoring of temperature and reaction time to prevent side reactions from growing. After forming an intermediate, it is reacted with 5-thiazolyl chloride in another solvent system, or assisted by an acid binding agent to smoothly convert it into the target product. < Br >
The reaction solvent is selected, depending on the reaction characteristics of each step, such as N, N-dimethylformamide, dichloromethane, etc. are all commonly used choices. The temperature control of the reaction is also the top priority. The early nucleophilic substitution may need to be warmed to tens of degrees Celsius, and the later acylation reaction may be near room temperature.

After the reaction is completed, the separation and purification of the product should also be cautious. A suitable solvent can be selected by recrystallization to precipitate the product, or it can be separated by column chromatography according to the polarity difference between the product and the impurities to obtain a high-purity product. < Br >
Preparation of this compound requires extremely high requirements for raw material control, reaction conditions, separation and purification techniques, so that the target product can be obtained for subsequent scientific research or industrial use.

What is the market outlook for n- (2-chloro-6-methylphenyl) -2- ((6-chloro-2-methyl-4-pyrimidinyl) amino) -5-thiazolecarboxamide?

Guanfu n- (2-chloro-6-methylphenyl) -2 - ((6-chloro-2-methyl-4-pyrimidinyl) amino) -5 -thiazolecarbonamide is still to be carefully observed in the market prospect.

Since the field of pharmaceutical research and development, such compounds often have unique pharmacological activities. Or because of the ingenious combination of chlorine, methyl and other groups in their structure, they have potential efficacy in targeting specific biomolecules. In the exploration of the treatment of various diseases such as antimalarial and antimicrobial, its delicate structure may make it closely fit with the key proteins of pathogens, just like the joint of mortise and tenon, thus hindering its physiological process and providing an opportunity for the creation of new drugs. If the road of research and development goes well, it may emerge in the market and gain the attention of the pharmaceutical industry.

However, there are many thorns on the road to the market. The cost of research and development is high, just like mountains and mountains. From laboratory synthesis, to clinical research, to multi-phase clinical trials, a huge amount of capital is required. And the competition is fierce, like a hundred competing. Many scientific research institutions and pharmaceutical companies are committed to the research and development of new drugs, and there are not a few studies of similar or similar structural compounds. If you want to stand out, you need to have unique advantages, or excellent efficacy, or better safety.

Furthermore, regulations and policies are like a curse of tight hoop. The drug approval process is complicated and rigorous, and the evaluation of its safety and effectiveness is meticulous. Only by strictly following it can you obtain marketing approval. If so, although there is hope in the future, the way forward needs to climb mountains and overcome thorns, and only then can you hope to gain a place in the market and contribute to human health and well-being.

N- (2-chloro-6-methylphenyl) -2- ((6-chloro-2-methyl-4-pyrimidinyl) amino) -5-thiazolecarboxamide What are the relevant Quality Standards?

This is a chemical substance named N- (2-chloro-6-methylphenyl) -2 - ((6-chloro-2-methyl-4-pyrimidinyl) amino) -5 -thiazolecarbonamide. The Quality Standards for this substance are covered by the following numbers.

The first is purity, which is the key quality standard. High purity of this substance can be used in scientific research, pharmaceuticals and other fields without hindrance. The presence of impurities may affect the course of its chemical reactions, or cause adverse effects in pharmaceutical applications. Therefore, its purity is usually required to reach a very high level, such as more than 98%, or even more than 99%, in order to meet the needs of many high-end applications.

The second is the relevant substance. It is necessary to carefully observe the relevant impurities derived during the production process, such as starting material residues, intermediate residues and degradation products. The content of such related substances must be strictly controlled. It may affect the stability, effectiveness and safety of the substance. The content of each related substance is often determined in detail by specific analytical methods, such as high-performance liquid chromatography (HPLC), and a strict upper limit is set.

The other is the appearance properties. The substance should have specific physical properties, such as color, crystal form, particle size, etc. Normally, it should be white or off-white crystalline powder. If the color is different or crystalline, the particle size is not compliant, or it suggests that the quality is flawed. This may affect the uniformity of mixing and dissolution in the process of pharmaceutical preparation.

There is also loss in drying. The amount of moisture or volatile impurities contained in the substance has a great impact on its quality stability. Therefore, it is necessary to determine the loss in drying to ensure that the content of moisture and volatile impurities is within a reasonable range. Generally, it is controlled below a certain percentage, such as 0.5% or 1.0%, to prevent the hydrolysis and mildew of the substance caused by excessive moisture.

The burning residue cannot be ignored. This indicator reflects the residual inorganic impurities of the substance after high temperature burning, and its content is too high, or it affects the purity and properties of the substance. It is often limited to a low level of incandescent residues, such as 0.1% or less, to ensure the purity of the substance.

In addition, content determination is also an important quality standard. By accurate analytical means, such as titration, spectroscopy, etc., the content of active ingredients of the substance is determined to ensure that it meets the established specifications, generally within a certain range of the marked amount, such as 95.0% - 105.0%.

These Quality Standards are indispensable in ensuring the quality and performance of N- (2-chloro-6-methylphenyl) -2 - ((6-chloro-2-methyl-4-pyrimidinyl) amino) -5 -thiazolecarbonamide, which is a criterion that must be strictly followed in the production and application process.