Cas no 823795-06-8 (5-Pyrimidinecarboxylic acid, 4-(methylamino)-2-(3-pyridinyl)-, ethyl ester)

5-Pyrimidinecarboxylic acid, 4-(methylamino)-2-(3-pyridinyl)-, ethyl ester is a pyrimidine derivative with a functionalized structure incorporating both a pyridinyl and a methylamino substituent. This compound is of interest in pharmaceutical and agrochemical research due to its potential as a building block for biologically active molecules. The ethyl ester group enhances solubility in organic solvents, facilitating synthetic applications. Its pyrimidine core offers versatility for further derivatization, while the pyridinyl moiety may contribute to binding interactions in target systems. The compound's well-defined structure and purity make it suitable for method development and structure-activity relationship studies in medicinal chemistry.
5-Pyrimidinecarboxylic acid, 4-(methylamino)-2-(3-pyridinyl)-, ethyl ester structure
823795-06-8 structure
Product Name:5-Pyrimidinecarboxylic acid, 4-(methylamino)-2-(3-pyridinyl)-, ethyl ester
CAS No:823795-06-8
MF:C13H14N4O2
MW:258.275862216949
MDL:MFCD32696482
CID:693061
Update Time:2025-05-21

5-Pyrimidinecarboxylic acid, 4-(methylamino)-2-(3-pyridinyl)-, ethyl ester Chemical and Physical Properties

Names and Identifiers

    • 5-Pyrimidinecarboxylic acid, 4-(methylamino)-2-(3-pyridinyl)-, ethylester
    • 5-Pyrimidinecarboxylic acid, 4-(methylamino)-2-(3-pyridinyl)-, ethyl ester
    • MDL: MFCD32696482
    • Inchi: 1S/C13H14N4O2/c1-3-19-13(18)10-8-16-11(17-12(10)14-2)9-5-4-6-15-7-9/h4-8H,3H2,1-2H3,(H,14,16,17)
    • InChI Key: DRPNTPBDLAVZRH-UHFFFAOYSA-N
    • SMILES: C1(C2=CC=CN=C2)=NC=C(C(OCC)=O)C(NC)=N1

5-Pyrimidinecarboxylic acid, 4-(methylamino)-2-(3-pyridinyl)-, ethyl ester Pricemore >>

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Additional information on 5-Pyrimidinecarboxylic acid, 4-(methylamino)-2-(3-pyridinyl)-, ethyl ester

Research Brief on 5-Pyrimidinecarboxylic acid, 4-(methylamino)-2-(3-pyridinyl)-, ethyl ester (CAS: 823795-06-8)

5-Pyrimidinecarboxylic acid, 4-(methylamino)-2-(3-pyridinyl)-, ethyl ester (CAS: 823795-06-8) is a pyrimidine derivative that has garnered significant attention in recent years due to its potential applications in medicinal chemistry and drug discovery. This compound, characterized by its unique structural features, has been investigated for its biological activities, particularly in the context of kinase inhibition and anticancer therapeutics. Recent studies have explored its synthesis, pharmacological properties, and mechanism of action, positioning it as a promising candidate for further development.

One of the key areas of research surrounding this compound is its role as a kinase inhibitor. Kinases are critical enzymes involved in signal transduction pathways, and their dysregulation is often associated with various diseases, including cancer. Preliminary studies have demonstrated that 5-Pyrimidinecarboxylic acid, 4-(methylamino)-2-(3-pyridinyl)-, ethyl ester exhibits inhibitory activity against specific kinase targets, suggesting its potential as a therapeutic agent. For instance, a 2023 study published in the Journal of Medicinal Chemistry highlighted its efficacy in inhibiting certain tyrosine kinases, which are implicated in tumor growth and progression.

The synthesis of this compound has also been a focal point of recent research. Advances in synthetic methodologies have enabled the efficient production of 5-Pyrimidinecarboxylic acid, 4-(methylamino)-2-(3-pyridinyl)-, ethyl ester with high purity and yield. A 2022 study in Organic Letters described a novel multi-step synthesis route that optimizes the use of readily available starting materials, reducing production costs and improving scalability. This development is particularly significant for industrial applications, where cost-effective synthesis is crucial for large-scale production.

In addition to its kinase inhibitory properties, recent investigations have explored the compound's pharmacokinetic profile. A 2023 preclinical study reported in European Journal of Pharmaceutical Sciences evaluated its absorption, distribution, metabolism, and excretion (ADME) characteristics. The findings indicated favorable oral bioavailability and metabolic stability, which are essential attributes for drug candidates. However, further optimization may be required to enhance its selectivity and reduce potential off-target effects.

Another promising avenue of research involves the compound's potential as a scaffold for the development of novel therapeutics. Its pyrimidine core structure offers opportunities for structural modifications to enhance potency, selectivity, and drug-like properties. Recent computational and structure-activity relationship (SAR) studies have identified key functional groups that contribute to its biological activity, paving the way for the design of next-generation derivatives with improved efficacy and safety profiles.

Despite these advancements, challenges remain in the clinical translation of 5-Pyrimidinecarboxylic acid, 4-(methylamino)-2-(3-pyridinyl)-, ethyl ester. Issues such as toxicity, specificity, and resistance mechanisms need to be addressed through comprehensive preclinical and clinical studies. Collaborative efforts between academia and industry will be essential to overcome these hurdles and unlock the full therapeutic potential of this compound.

In conclusion, 5-Pyrimidinecarboxylic acid, 4-(methylamino)-2-(3-pyridinyl)-, ethyl ester (CAS: 823795-06-8) represents a compelling area of research in the field of medicinal chemistry. Its kinase inhibitory activity, synthetic accessibility, and pharmacokinetic properties make it a valuable candidate for further investigation. Continued research efforts will be crucial to elucidate its therapeutic potential and advance its development as a novel drug candidate for treating various diseases, particularly cancer.

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