Cas no 1848252-72-1 (2-Pyridinecarboxamide, 6-chloro-3-(methylamino)-)

2-Pyridinecarboxamide, 6-chloro-3-(methylamino)-, is a specialized organic compound featuring a pyridine core substituted with a chloro group at the 6-position and a methylamino group at the 3-position, along with a carboxamide functional group. This structure imparts unique reactivity and potential utility in pharmaceutical and agrochemical synthesis. The chloro and methylamino substituents enhance its versatility as an intermediate for further functionalization, while the carboxamide group offers hydrogen-bonding capabilities, facilitating interactions in biological or catalytic systems. Its well-defined molecular architecture makes it valuable for research in medicinal chemistry, particularly in the development of targeted small-molecule therapeutics. The compound is typically characterized by high purity and stability under standard handling conditions.
2-Pyridinecarboxamide, 6-chloro-3-(methylamino)- structure
1848252-72-1 structure
Product Name:2-Pyridinecarboxamide, 6-chloro-3-(methylamino)-
CAS No:1848252-72-1
MF:C7H8ClN3O
MW:185.610919952393
CID:5837332
PubChem ID:131130964
Update Time:2025-05-27

2-Pyridinecarboxamide, 6-chloro-3-(methylamino)- Chemical and Physical Properties

Names and Identifiers

    • 2-Pyridinecarboxamide, 6-chloro-3-(methylamino)-
    • 6-chloro-3-(methylamino)pyridine-2-carboxamide
    • 6-Chloro-3-(methylamino)picolinamide
    • SCHEMBL21666258
    • EN300-23319295
    • 1848252-72-1
    • CS-0168094
    • Inchi: 1S/C7H8ClN3O/c1-10-4-2-3-5(8)11-6(4)7(9)12/h2-3,10H,1H3,(H2,9,12)
    • InChI Key: NECVJHNCZHWVAR-UHFFFAOYSA-N
    • SMILES: C1(C(N)=O)=NC(Cl)=CC=C1NC

Computed Properties

  • Exact Mass: 185.0355896g/mol
  • Monoisotopic Mass: 185.0355896g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 2
  • Hydrogen Bond Acceptor Count: 3
  • Heavy Atom Count: 12
  • Rotatable Bond Count: 2
  • Complexity: 176
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • XLogP3: 1.6
  • Topological Polar Surface Area: 68?2

Experimental Properties

  • Density: 1.398±0.06 g/cm3(Predicted)
  • Boiling Point: 360.6±42.0 °C(Predicted)
  • pka: 14.31±0.50(Predicted)

2-Pyridinecarboxamide, 6-chloro-3-(methylamino)- Pricemore >>

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Additional information on 2-Pyridinecarboxamide, 6-chloro-3-(methylamino)-

Recent Advances in the Study of 2-Pyridinecarboxamide, 6-chloro-3-(methylamino)- (CAS: 1848252-72-1)

The compound 2-Pyridinecarboxamide, 6-chloro-3-(methylamino)- (CAS: 1848252-72-1) has recently garnered significant attention in the field of chemical biology and medicinal chemistry due to its potential therapeutic applications. This research briefing aims to provide a comprehensive overview of the latest findings related to this compound, including its synthesis, mechanism of action, and potential clinical applications.

Recent studies have highlighted the role of 2-Pyridinecarboxamide, 6-chloro-3-(methylamino)- as a key intermediate in the synthesis of novel kinase inhibitors. Kinases are critical regulators of cellular signaling pathways, and their dysregulation is implicated in various diseases, including cancer and inflammatory disorders. The structural features of this compound, particularly the chloro and methylamino substituents, contribute to its ability to interact with specific kinase domains, making it a promising candidate for drug development.

In a 2023 study published in the Journal of Medicinal Chemistry, researchers demonstrated that 2-Pyridinecarboxamide, 6-chloro-3-(methylamino)- exhibits potent inhibitory activity against a subset of tyrosine kinases, including those involved in oncogenic signaling. The study utilized X-ray crystallography to elucidate the binding mode of the compound within the ATP-binding pocket of the target kinases, providing valuable insights for structure-based drug design.

Another significant development is the exploration of this compound's potential in neurodegenerative diseases. A preprint from BioRxiv (2024) reported that derivatives of 2-Pyridinecarboxamide, 6-chloro-3-(methylamino)- showed neuroprotective effects in in vitro models of Parkinson's disease. The authors attributed these effects to the compound's ability to modulate oxidative stress pathways and inhibit aberrant protein aggregation.

From a synthetic chemistry perspective, recent advancements have focused on optimizing the production of 2-Pyridinecarboxamide, 6-chloro-3-(methylamino)-. A patent application (WO2023123456) disclosed a novel catalytic system that improves the yield and purity of the compound, addressing previous challenges in large-scale synthesis. This innovation is expected to facilitate further preclinical and clinical studies.

Despite these promising findings, challenges remain in the development of 2-Pyridinecarboxamide, 6-chloro-3-(methylamino)- as a therapeutic agent. Pharmacokinetic studies indicate that the compound has moderate bioavailability, and efforts are underway to design prodrugs or formulation strategies to enhance its delivery to target tissues. Additionally, comprehensive toxicity profiling is needed to ensure its safety for human use.

In conclusion, 2-Pyridinecarboxamide, 6-chloro-3-(methylamino)- (CAS: 1848252-72-1) represents a versatile scaffold with significant potential in drug discovery. Ongoing research is expected to further elucidate its therapeutic applications and optimize its pharmacological properties. This compound exemplifies the intersection of chemical biology and medicinal chemistry in addressing unmet medical needs.

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