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1-Piperidinebutanoic Acid, 4- [ (4-Chlorophenyl) -2-Pyridinylmethoxy] -, (S) -, what is the chemical structure of Monobenzenesulfonate
The name of this compound is (S) -4- [ (4-chlorophenyl) -2-pyridylmethoxy] -1-piperidinobutyric acid monophenesulfonate.
Looking at its name, its structure can be analyzed. " (S) " shows that it has chirality and shows a specific stereoconfiguration. "4- [ (4-chlorophenyl) -2-pyridylmethoxy]", it can be seen that a complex substituent is connected at the 4th position of the main chain. This substituent contains 4-chlorophenyl and 2-pyridyl, and the two are connected by methoxy. "1-piperidinobutyric acid" indicates that the main chain is composed of a piperidine ring connected to butyric acid, and the piperidine ring is connected to the 1 position of butyric acid "Monobenzenesulfonate" is the salt formed by this acid and benzenesulfonic acid.
In summary, the structure of this compound contains chiral centers, the main chain is connected with piperidine and butyric acid, and 4 positions are connected with specific substituents, and form benzenesulfonate form, which gives it unique chemical properties and potential uses.
1-Piperidinebutanoic Acid, 4- [ (4-Chlorophenyl) -2-Pyridinylmethoxy] -, (S) -, What are the main uses of Monobenzenesulfonate
1-Piperidinobutyric acid, 4- [ (4-chlorophenyl) -2-pyridyl methoxy] -, (S) -, monophenylsulfonate, this drug is widely used. It is often used as a key active ingredient in the field of medicine, participating in the development of many drugs, and is of great significance for the treatment of specific diseases. For example, in neurological diseases, it can precisely interact with human targets through unique chemical structures, or regulate neurotransmitter transmission, or repair damaged nerve cells, providing assistance for alleviating diseases and improving the quality of life of patients.
In the path of scientific research and exploration, it is like a key, opening the door for researchers to further study related physiological and pathological mechanisms. Scientists can use it to explore cell signaling pathways, clarify the root causes of disease development, and lay the foundation for the development of more effective treatments.
In the chemical industry, this compound also has a place. Because of its specific chemical properties, or can be used to synthesize materials with special properties, these materials are very useful in coatings, plastics and other fields, giving products excellent characteristics such as better stability and corrosion resistance, thereby enhancing product quality and market competitiveness.
1-Piperidinebutanoic Acid, 4- [ (4-Chlorophenyl) -2-Pyridinylmethoxy] -, (S) -, Monobenzenesulfonate
To prepare 1-piperidinobutyric acid, 4- [ (4-chlorophenyl) -2 -pyridyl methoxy] -, (S) -, monobenzene sulfonate, the method is as follows:
First, various raw materials need to be prepared, such as piperidine derivatives containing specific substituents, halogens with corresponding chlorophenyl and pyridyl structures, and benzene sulfonic acid.
First, in a suitable reaction vessel, an anhydrous organic solvent such as toluene, dichloromethane, etc. is used to create a reaction environment, and piperidine derivatives are added, followed by an appropriate amount of bases, such as potassium carbonate, sodium carbonate, etc., to activate the reaction check point. The halogen is slowly added dropwise. This process requires temperature control to ensure a smooth reaction and not to overdo it. After nucleophilic substitution, the specific check point of the piperidine derivative is connected to the group where the halogen atom in the halogen is located, and the key intermediate is obtained.
Subsequently, the intermediate is separated by chiral means, such as chiral column chromatography, to obtain a product with the (S) configuration. This product is then reacted with benzenesulfonic acid in a suitable solvent, such as ethanol, to adjust the pH and form monophenesulfonate. After the reaction, after concentration, crystallization, filtration, drying and other post-processing processes, pure 1-piperidinobutyric acid, 4- [ (4-chlorophenyl) -2-pyridyl methoxy] -, (S) -, monobenzene sulfonate can be obtained. During the whole process, the precise control of the reaction conditions and the proper preparation of the proportion of raw materials are the keys to the successful preparation of the target product.
1-Piperidinebutanoic Acid, 4- [ (4-Chlorophenyl) -2-Pyridinylmethoxy] -, (S) -, What are the pharmacological properties of Monobenzenesulfonate
(This drug) 1-piperidinbutyric acid, 4- [ (4-chlorophenyl) -2-pyridyl methoxy] -, (S) -, monobenzenesulfonate, its pharmacological properties are as follows:
This drug has a unique effect and can precisely act on specific targets in the body. It can affect the relevant cell signaling pathways, thereby regulating the physiological functions of the body. In terms of drug efficacy, it can bind to receptors in a more efficient way, showing good affinity and specificity.
From a metabolic point of view, after entering the human body, it will be decomposed and transformed according to the body's metabolic laws. Some of the ingredients can be metabolized by the liver and excreted in the form of certain metabolites, and the metabolic process is relatively stable, which will not cause excessive burden on other important organ functions.
At the same time, the distribution of this drug in the body is selective, and it can be enriched in specific tissues and organs to better exert the therapeutic effect. In terms of safety, many studies have verified that under conventional doses, there are relatively few adverse reactions, which is well tolerated and can provide a more reliable guarantee for the treatment of patients, and help the improvement and recovery of the disease.
1-Piperidinebutanoic Acid, 4- [ (4-Chlorophenyl) -2-Pyridinylmethoxy] -, (S) -, What are the precautions when using Monobenzenesulfonate
1-Piperidinobutyric acid, 4- [ (4-chlorophenyl) -2-pyridylmethoxy] -, (S) -, monophenylsulfonate, many matters need to be paid attention to when using this medicine. Its nature is different, and it must be used with caution.
First, follow the doctor's advice and do not change the dose without authorization. The doctor determines the dose according to the patient's illness, physical condition and other conditions, and increases or decreases the dose without authorization, or causes the drug effect to fail, or even causes adverse reactions. If the dosage is too small, the disease will be difficult to cure; if the dosage is too much, it may damage the viscera.
The second time is to pay attention to adverse reactions. During the medication, pay attention to physical changes, such as nausea, vomiting, dizz If there is an adverse reaction, tell the doctor immediately, dispose of it according to the doctor's suggestion, or adjust the medicine, or stop taking it.
Furthermore, avoid interaction with other medicines when taking medicine. Inform the doctor of all medicines used, including prescription medicines, over-the-counter medicines, herbal medicines, etc. Because of other medicines or mutual interference with them, the efficacy of the medicine will change or increase the risk.
In addition, specific groups of people should be cautious when taking medicine. Pregnant women, breastfeeding women, children, the elderly, etc., have different constitutions or physiological functions than ordinary people, and the use of drugs may have different risks. Pregnant women and breastfeeding women use drugs, or harm the fetus and infants; children are not fully developed, and the function of the elderly's organs will decline. All need to be decided by the doctor after weighing the advantages and
In short, when using this medicine, it is necessary to strictly follow the doctor's advice, closely observe the body's reaction, and consult the doctor immediately in case of suspicion to ensure the safety and effectiveness of the medication.