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Mithramycin A CAS:1101120-86-8

Tert-butyl 3-acetylpyrazolo[1,5-a]pyridin-5-ylcarbamate is a compound with potential pharmaceutical significance due to its unique structural features. The tert-butyl group attached to the nitrogen atom provides steric hindrance, influencing the molecule’s reactivity and pharmacokinetic properties. The pyrazolo[1,5-a]pyridine core is a privileged scaffold in medicinal chemistry, known for its diverse biological activities. The acetyl moiety introduces polarity and potential hydrogen bonding capabilities, impacting the compound’s interactions with biological targets. This introduction aims to explore the synthesis, structural characteristics, and potential pharmacological applications of tert-butyl 3-acetylpyrazolo[1,5-a]pyridin-5-ylcarbamate.


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Application and Effect:

The synthesis of tert-butyl 3-acetylpyrazolo[1,5-a]pyridin-5-ylcarbamate typically involves multistep procedures, starting from commercially available starting materials. One common route involves the condensation of pyrazole and pyridine precursors, followed by acetylation and carbamylation steps to introduce the acetyl and tert-butylcarbamate functionalities, respectively. Spectroscopic techniques such as NMR, IR, and mass spectrometry are employed to confirm the structure and purity of the synthesized compound. The molecular structure of tert-butyl 3-acetylpyrazolo[1,5-a]pyridin-5-ylcarbamate exhibits planarity due to conjugation within the pyrazolo[1,5-a]pyridine ring system. The tert-butyl group introduces bulkiness, potentially affecting the compound's solubility and membrane permeability. Furthermore, the presence of the acetyl group imparts polarity and potential for hydrogen bonding interactions, which can influence the compound's binding affinity to biological targets. Pharmacological Significance and Potential Applications The structural features of tert-butyl 3-acetylpyrazolo[1,5-a]pyridin-5-ylcarbamate make it a promising candidate for pharmaceutical research and development. The pyrazolo[1,5-a]pyridine scaffold is known to exhibit a wide range of biological activities, including anticancer, antimicrobial, and anti-inflammatory properties. Additionally, the tert-butylcarbamate moiety can enhance the compound's metabolic stability and bioavailability, potentially improving its pharmacokinetic profile. The acetyl group in tert-butyl 3-acetylpyrazolo[1,5-a]pyridin-5-ylcarbamate may facilitate interactions with specific enzyme targets through hydrogen bonding or hydrophobic interactions. This could lead to the development of novel therapeutic agents targeting various diseases, including cancer, infectious diseases, and neurological disorders. In conclusion, tert-butyl 3-acetylpyrazolo[1,5-a]pyridin-5-ylcarbamate represents a structurally intriguing compound with potential pharmaceutical significance. Further research into its synthesis, structure-activity relationships, and pharmacological applications is warranted to fully explore its therapeutic potential in various disease contexts.

Product Sample:

L-Arginine1
L-Arginine2

Product Packing:

L-Arginin3

Additional Information:

Composition C14H17N3O3
Assay 99%
Appearance white powder
CAS No.  1101120-86-8
Packing Small and bulk
Shelf Life 2 years
Storage Store in cool and dry area
Certification ISO.

 


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