CAS 1196153-97-5
:Ethyl 7-aminopyrazolo[1,5-a]pyrimidine-3-carboxylate
Description:
Ethyl 7-aminopyrazolo[1,5-a]pyrimidine-3-carboxylate is a chemical compound characterized by its unique pyrazolo-pyrimidine structure, which incorporates both a pyrazole and a pyrimidine ring. This compound features an ethyl ester functional group, contributing to its solubility and reactivity. The presence of an amino group at the 7-position of the pyrazolo ring enhances its potential for biological activity, making it of interest in medicinal chemistry. The carboxylate moiety at the 3-position plays a crucial role in the compound's reactivity and interaction with biological targets. Ethyl 7-aminopyrazolo[1,5-a]pyrimidine-3-carboxylate may exhibit various pharmacological properties, including potential anti-inflammatory or anti-cancer activities, although specific biological effects would depend on further empirical studies. Its molecular structure allows for diverse synthetic modifications, which can lead to the development of derivatives with enhanced efficacy or selectivity. Overall, this compound represents a valuable scaffold in drug discovery and development, particularly in the context of targeting specific enzymes or receptors in biological systems.
Formula:C9H10N4O2
InChI:InChI=1S/C9H10N4O2/c1-2-15-9(14)6-5-12-13-7(10)3-4-11-8(6)13/h3-5H,2,10H2,1H3
InChI key:InChIKey=YSYFACLHRFMDES-UHFFFAOYSA-N
SMILES:C(OCC)(=O)C1=C2N(N=C1)C(N)=CC=N2
Synonyms:- Pyrazolo[1,5-a]pyrimidine-3-carboxylic acid, 7-amino-, ethyl ester
- Ethyl 7-aminopyrazolo[1,5-a]pyrimidine-3-carboxylate
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