As a leading (S)-Diethyl 2-(4-(2-(2-Amino-4-Oxo-4,7-Dihydro-3H-Pyrrolo[2,3-D]Pyrimidin-5-Yl)Ethyl)Benzamido)Pentanedioate 4-Methylbenzenesulfonate 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 (S) -Diethyl 2- (4- (2- (2- (2-Amino-4-Oxo-4, 7-Dihydro-3H-Pyrrolo [2,3-D] Pyrimidin-5-Yl) Ethyl) Benzamido) Pentanedioate 4-Methylbenzenesulfonate?
(This is the name of a chemical substance written in modern chemical nomenclature. It is said in ancient Chinese to help you clarify its meaning.) This " (S) -diethyl2- (4- (2- (2-amino-4-oxo-4,7-dihydro-3H-pyrrolido [2,3-d] pyrimidine-5-yl) ethyl) benzamido) glutarate 4-methylbenzene sulfonate" is an organic compound. Looking at its name, it can be seen that this compound has a complex structure. Among them, " (S) " indicates its three-dimensional configuration and has a specific spatial arrangement. "Diethyl" indicates that there are two ethyl groups connected in the molecule. The ester part of glutarate is the ester structure formed by the esterification reaction of glutaric acid and ethanol. "2- (4- (2- (2-amino-4-oxo-4,7-dihydro-3H-pyrrolido [2,3-d] pyrimidine-5-yl) ethyl) benzamido) ", this long chain structure includes complex cyclic systems such as benzene rings and pyrrolido-pyrimidine rings, and the rings are connected with specific functional groups such as amino groups and oxo groups. Amino groups are basic, and oxo groups affect the electron cloud distribution and chemical activity of molecules. As for "4-methylbenzenesulfonate", it is the salt structure formed by this compound and 4-methylbenzenesulfonate. Such compounds are often used in organic synthesis, medicinal chemistry, and other fields, or as potential pharmaceutical active ingredients, or as key intermediates in organic synthesis reactions. They can participate in many complex chemical reactions and use their unique structures and activities to build more complex organic molecules to serve the research and application of medicine, materials, and many other fields.
What is the chemical structure of (S) -Diethyl 2- (4- (2- (2-Amino-4-Oxo-4, 7-Dihydro-3H-Pyrrolo [2,3-D] Pyrimidin-5-Yl) Ethyl) Benzamido) Pentanedioate 4-Methylbenzenesulfonate?
This is a question about the chemical structure of (S) -diethyl2- (4- (2- (2-amino-4-oxo-4,7-dihydro-3H-pyrrolo [2,3-d] pyrimidine-5-yl) ethyl) benzamido) glutarate 4-methylbenzenesulfonate. To understand this chemical structure, it is necessary to name it.
The main body of (S) -diethyl2- (4- (2- (2-amino-4-oxo-4,7-dihydro-3H-pyrrolido [2,3-d] pyrimidine-5-yl) ethyl) benzamido) glutarate, glutarate as the root, diethyl group is connected to the carboxyl group of glutaric acid, and it has an ester structure. The 2-position is connected with a long chain substituent, which contains a benzamide group, the nitrogen of the amide group is connected to the 2-position carbon of the glutarate ester, and the 4-position of the benzene ring is connected with an ethyl group containing 2- (2-amino-4-oxo-4,7-dihydro-3H-pyrrolido [2,3-d] pyrimidine-5-yl). The pyrrolido [2,3-d] pyrimidine ring has a specific parallel ring structure, and the 2-amino, 4-oxo and other substituents are in the corresponding positions.
Furthermore, 4-methylbenzenesulfonate is its salt-forming part, 4-methylbenzenesulfonate ion forms a salt with the basic part of the main structure, or provides proton acceptance check points for amino groups and the like to form a salt structure.
In this way, after detailed analysis of each part, the chemical structure of (S) -diethyl2- (4- (2- (2-amino-4-oxo-4,7-dihydro-3H-pyrrolido [2,3-d] pyrimidine-5-yl) ethyl) benzamido) glutarate 4-benzenesulfonate can be obtained.
What are the applications of (S) -Diethyl 2- (4- (2- (2- (2-Amino-4-Oxo-4, 7-Dihydro-3H-Pyrrolo [2,3-D] Pyrimidin-5-Yl) Ethyl) Benzamido) Pentanedioate 4-Methylbenzenesulfonate?
(S) -diethyl2- (4- (2- (2-amino-4-oxo-4,7-dihydro-pyrrolido [2,3-d] pyrimidine-5-yl) ethyl) benzamido) glutarate 4-methylbenzene sulfonate, this compound may have extraordinary uses in the field of medicine.
To observe the structure of this compound, it contains a specific pyrrolidine structure, which is often found in anti-cancer drugs. It may be possible to intervene in key biological processes in cancer cells, such as inhibiting the activity of specific protein kinases, which play a key role in cancer cell proliferation, survival and metastasis, and then achieve anti-cancer effects. The glutarate and benzamide moiety may have important effects on the pharmacokinetic properties of the compound, such as solubility and membrane permeability, which are related to whether the drug can effectively reach the target of action.
Furthermore, 4-methylbenzene sulfonate, as a salt form, may improve the stability and solubility of the compound, making it easier to make suitable dosage forms, such as tablets, injections, etc., during the development of preparations, to facilitate clinical application.
However, the specific efficacy of this compound still needs to be verified by rigorous pharmacological experiments and clinical trials. Although it is speculated to have potential medicinal value from the structure, the practical application still needs to be fully and deeply studied before its true utility and safety in the treatment of diseases can be determined.
What is the synthesis method of (S) -Diethyl 2- (4- (2- (2- (2-Amino-4-Oxo-4, 7-Dihydro-3H-Pyrrolo [2,3-D] Pyrimidin-5-Yl) Ethyl) Benzamido) Pentanedioate 4-Methylbenzenesulfonate?
To prepare (S) -diethyl 2- (4- (2- (2-amino-4-oxo-4,7-dihydro-3H-pyrrolido [2,3-d] pyrimidine-5-yl) ethyl) benzamido) glutarate 4-methylbenzene sulfonate, the method is as follows:
First take an appropriate amount of 2- (4- (2- (2-amino-4-oxo-4,7-dihydro-3H-pyrrole And [2,3 - d] pyrimidine-5 - yl) ethyl) benzoic acid as a starting material, place it in a reactor, add an appropriate amount of ethylene diester reagents, and add a suitable catalyst, this catalyst can promote the condensation reaction between the two. During the reaction, attention should be paid to temperature control to maintain the temperature within a certain range to ensure the smooth progress of the reaction and prevent the formation of side reactions. After the reaction is completed, the product is purified by ordinary separation methods such as extraction, distillation, recrystallization, etc., to obtain (S) -diethyl 2- (4 - (2 - (2 - amino - 4 - oxo - 4,7 - dihydro - 3H - pyrrolo [2,3 - d] pyrimidine - 5 - yl) ethyl) benzamido) glutarate.
Then, the resulting esteride is mixed with 4-methylbenzenesulfonic acid in a certain molar ratio, an appropriate amount of organic solvent is added, and under suitable temperature and stirring conditions, the two undergo a salt-forming reaction. During this reaction process, the reaction process needs to be closely monitored, which can be measured by means of thin-layer chromatography. After the reaction is complete, the (S) -diethyl 2 - (4 - (2 - amino - 4 - oxo - 4,7 - dihydro - 3H - pyrrolido [2,3 - d] pyrimidine - 5 - yl) ethyl) benzamido) glutarate 4 - methylbenzene sulfonate can be obtained by filtration, washing, drying and other steps. The whole synthesis process must strictly abide by the operating procedures and pay attention to the control of each reaction condition to obtain the target product with high purity.
What are the physicochemical properties of (S) -Diethyl 2- (4- (2- (2-Amino-4-Oxo-4, 7-Dihydro-3H-Pyrrolo [2,3-D] Pyrimidin-5-Yl) Ethyl) Benzamido) Pentanedioate 4-Methylbenzenesulfonate?
(S) -diethyl 2 - (4 - (2 - amino - 4 - oxo - 4,7 - dihydro - 3H - pyrrolido [2,3 - d] pyrimidine - 5 - yl) ethyl) benzamido) glutarate 4 - methylbenzene sulfonate, this is an organic compound. Its physical and chemical properties are quite important, related to its application in many fields.
First of all, the appearance is usually white to off-white crystalline powder, which is delicate and uniform. This appearance feature is easy to identify and make preliminary judgments. Looking at it like the first fall of snow, it is delicate and pure, making people know its texture at a glance.
In terms of solubility, it has a certain solubility in organic solvents such as methanol and ethanol, just like fish get water, which can be well dispersed. However, the solubility in water is relatively low, like a boulder entering water, it is difficult to completely dissolve. This difference in solubility is of great significance to the development of its formulations. The solubility in different solvents is different, which can affect the choice of drug formulations and dosage forms.
Melting point is also a key property. After determination, the melting point of the compound is in a specific range. This characteristic is like the "personality temperature" of the substance, which plays an extraordinary role in identification and purity detection. Accurate melting point data is like a key, which can open the door to the identification of compound purity and authenticity. In terms of stability,
is relatively stable in dry and cool environments. In case of high temperature, high humidity or strong light exposure, its structure and properties may change, just like a delicate flower in the event of strong winds and rain, it is easy to lose its original appearance. This stability feature needs to be considered during storage and transportation, and it is necessary to create a suitable environment for it to ensure its quality.
The above physical and chemical properties are of key value in the fields of drug research and development, chemical production, etc., and are the basis for in-depth understanding and rational application of this compound.