2 1e 1 4 Methylphenyl 3 Pyrrolidin 1 Ylprop 1 En 1 Yl Pyridine Hydrochloride
pyridine pyrrole pyrazine piperidine piperazine

2-[(1E)-1-(4-methylphenyl)-3-pyrrolidin-1-ylprop-1-en-1-yl]pyridine hydrochloride

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    150402

    Chemical Name 2-[(1E)-1-(4-methylphenyl)-3-pyrrolidin-1-ylprop-1-en-1-yl]pyridine hydrochloride

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    General Information
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    Frequently Asked Questions

    As a leading 2-[(1E)-1-(4-methylphenyl)-3-pyrrolidin-1-ylprop-1-en-1-yl]pyridine hydrochloride supplier, we deliver high-quality products across diverse grades to meet evolving needs, empowering global customers with safe, efficient, and compliant chemical solutions.

    What is the chemical structure of 2- [ (1E) -1- (4-methylphenyl) -3-pyrrolidin-1-ylprop-1-en-1-yl] pyridine hydrochloride
    This is the chemical structure analysis of 2 - [ (1E) -1- (4-methylphenyl) -3-pyrrolidine-1-ylpropyl-1-ene-1-yl] pyridine hydrochloride. To understand its structure, we need to look at the main pyridine ring, which is the core structure. In the second position of the pyridine ring, there is a substituent. This substituent contains an allyl structure, and the first position of the allyl is connected with (4-methylphenyl) and the third position is connected with a pyrrolidine group. In this case, the double bond configuration of the allyl group is E-type, which means the trans at the larger group at both ends of the double bond. The salt of hydrochloride is the salt of the organic base and hydrochloric acid. The nitrogen atom of the organic base binds hydrogen ions, and the chloride ions balance the charge with it. In this way, the chemical structure of 2 - [ (1E) -1- (4-methylphenyl) -3-pyrrolidine-1-ylpropyl-1-ene-1-yl] pyridine hydrochloride is obtained.
    What are the physical properties of 2- [ (1E) -1- (4-methylphenyl) -3-pyrrolidin-1-ylprop-1-en-1-yl] pyridine hydrochloride
    2 - [ (E) - 1 - (4 - methylphenyl) - 3 - pyrrolidine - 1 - ylpropyl - 1 - ene - 1 - yl] pyridine hydrochloride, this is an organic compound. Its physical properties are quite important, related to its application in different scenarios.
    Looking at its appearance, it is usually white to white-like crystalline powder. This morphology is conducive to identification and processing, and in the field of pharmaceutical preparation, this appearance is easy to observe and control. Its solubility is also critical. The compound has a certain solubility in organic solvents such as methanol and ethanol, and can also be dissolved in water. This property makes it flexible in reactions or formulations of different solvent systems. For example, in drug development, according to its solubility, a suitable solvent can be selected for dissolution to achieve the best efficacy.
    Melting point is an important physical parameter, about 170-175 ° C. Determination of melting point can assist in the identification of compound purity. If the actual melting point is close to the standard value, it indicates that the purity is high; if the deviation is large, or impurities are mixed in. Like in the quality control link, melting point detection is a key step.
    In terms of stability, it is relatively stable at room temperature and pressure, but it is necessary to avoid contact with strong oxidants, strong acids and other substances. Due to the structure containing pyridine rings and pyrrolidyl groups, specific chemical substances may cause reactions, cause structural changes, and affect performance. If stored, pay attention to the surrounding environment and do not co-locate with unsuitable substances.
    The physical properties of this compound are interrelated, laying the foundation for its application in chemical, pharmaceutical and other fields. During the research and development and production process, these properties need to be accurately considered to achieve the best results.
    What is the use of 2- [ (1E) -1- (4-methylphenyl) -3-pyrrolidin-1-ylprop-1-en-1-yl] pyridine hydrochloride
    2-%5B%281E%29-1-%284-Methylphenyl% 29-3-pyrrolidine-1-ylpropyl-1-ene-1-yl% 5D pyridine hydrochloride is an organic compound. It has a wide range of uses in the field of medicine and is often used as a key intermediate in drug synthesis. Through subtle chemical reactions, it can be cleverly combined with other compounds to construct drug molecules with more complex structures and more unique effects, bringing hope for the treatment of many diseases.
    In the process of scientific research and exploration, scientists have used their unique chemical structure to deeply explore the mechanism of organic reactions, clarify the breaking and recombination of chemical bonds during the reaction process, and gain insight into the essence of the reaction, in order to promote the development and progress of organic chemistry theory. At the same time, in the field of materials science, it has also emerged. After specific processing, materials can be endowed with special optical and electrical properties, which can contribute to the research and development of new functional materials.
    As "Tiangong Kaiwu" said: "Everything in the world has its use." Although this compound is small, it plays a key role in different fields, helping humans to continuously forge ahead in medicine, scientific research, materials, etc., and move towards a better future.
    2- [ (1E) -1- (4-methylphenyl) -3-pyrrolidin-1-ylprop-1-en-1-yl] pyridine hydrochloride
    To prepare 2 - [ (1E) - 1 - (4 - methylphenyl) - 3 - pyrrolidine - 1 - propyl - 1 - ene - 1 - yl] pyridine hydrochloride, the method is as follows.
    First take an appropriate amount of 4 - methylacetophenone, place it in a clean reaction vessel, and fully replace the air with nitrogen to create an inert atmosphere. Then add a suitable base, such as potassium tert-butoxide, stir well to fully dissolve the base. This process needs to pay attention to temperature changes and maintain it within a moderate range to prevent side reactions from occurring. < Br >
    Take another pyrrolidine and acronaldehyde, and slowly add them dropwise to the above reaction system according to a specific molar ratio. When adding dropwise, the speed should be slow, and the stirring should be continued to allow the reactants to fully contact and react. This reaction may be a nucleophilic addition process, generating key intermediates.
    After a period of reaction, the reaction progress should be monitored by thin-layer chromatography or other suitable analytical means. When the reaction reaches the desired level, the reaction is terminated. Then, the reaction mixture is post-treated. With a dilute acid solution, such as dilute hydrochloric acid, carefully adjust the pH value of the system to stabilize the intermediate. Then, an organic solvent, such as ethyl acetate, is used to extract the product. After multiple extractions, the organic phases were combined and dried with anhydrous sodium sulfate to remove the moisture.
    After that, the dried organic phase was distilled under reduced pressure to remove the organic solvent to obtain a crude product. The crude product was further purified by column chromatography, and a suitable eluent was selected, such as a mixed solvent of petroleum ether and ethyl acetate. According to the difference in the partition coefficient between the product and the impurity in the stationary phase and the mobile phase, the product and the impurity were separated to obtain a pure 2 - [ (1E) -1- (4-methylphenyl) -3-pyrrolidine-1-ylpropyl-1-ene-1-yl] pyridine.
    Finally, the product is dissolved in an appropriate amount of anhydrous ether, and dried hydrogen chloride gas is introduced to form the product into a salt, which is 2 - [ (1E) - 1 - (4 - methylphenyl) - 3 - pyrrolidine - 1 - yl propyl - 1 - ene - 1 - yl] pyridine hydrochloride. The obtained product was determined by melting point, nuclear magnetic resonance analysis, etc. to confirm its structure and purity.
    What is the safety of 2- [ (1E) -1- (4-methylphenyl) -3-pyrrolidin-1-ylprop-1-en-1-yl] pyridine hydrochloride
    2-%5B%281E%29-1-%284-methylphenyl%29-3-pyrrolidin-1-ylprop-1-en-1-yl%5Dpyridine hydrochloride, which is a complex organic compound. Its safety considerations are related to multiple ends.
    During chemical synthesis operations, many raw materials and reaction processes may be at risk. The reagents used in synthesis may be toxic, corrosive, and flammable. If some organic solvents are flammable and explosive, and the volatile gas can cause damage to the human respiratory tract and nervous system. Some reactants or intermediate products may be highly irritating to the skin and eyes, and inadvertent contact can cause burns.
    Although the product itself has not been studied in detail to disclose all its characteristics, it contains pyridine and pyrrolidine structures. Such structural compounds may have certain biological activities. After entering the organism, or interfere with physiological processes. Such as affecting the transmission of neurotransmitters in the nervous system and interfering with cellular metabolic pathways. However, its specific toxicity, teratogenicity, carcinogenicity, etc., need to be investigated in detail by professional toxicology experiments.
    In terms of the environment, if such compounds are not properly handled and discharged, or accumulate and migrate in the environment. Because of its complex structure, it is difficult to degrade naturally, or cause long-term effects on soil and water ecosystems, interfering with the structure and function of biological communities.
    To fully clarify its safety, in-depth research is required in many aspects. From chemical synthesis practices to ensure the safety of personnel, to toxicological experiments to determine the impact on organisms, to environmental behavior studies to understand the impact on ecosystems. In this way, the safety of 2-%5B%281E%29-1-%284-methylphenyl%29-3-pyrrolidin-1-ylprop-1-en-1-yl%5Dpyridine hydrochloride can be fully evaluated.