5466-67-1

Usage

Uses

Used in Medicinal Chemistry:
2-(cyanomethyl)-5,7-dimethylpyrazolo[1,5-a]pyrimidine-3-carbonitrile is used as a potential pharmaceutical candidate for the development of new drugs, leveraging its unique chemical structure to target specific biological pathways or receptors.
Used in Material Science:
In the field of material science, 2-(cyanomethyl)-5,7-dimethylpyrazolo[1,5-a]pyrimidine-3-carbonitrile may be utilized as a component in the synthesis of novel materials with specific properties, such as high thermal stability or unique electronic characteristics, due to its heterocyclic nature and functional groups.
Used in Chemical Research:
As a heterocyclic compound with a distinctive structure, 2-(cyanomethyl)-5,7-dimethylpyrazolo[1,5-a]pyrimidine-3-carbonitrile serves as a subject of study in chemical research, where its properties, reactivity, and potential applications are explored to expand the understanding of heterocyclic chemistry and its implications in various industries.

Upstream product

• 123-54-6 acetylacetone 
• 54711-21-6 5-amino-3-(cyanomethyl)-1H-pyrazole-4-carbonitrile 
• 64-17-5 ethanol 
• 917-58-8 potassium ethoxide 

Relevant academic research and scientific papers

Pyrazolo[1,5-a]Pyrimidine Derivative as Precursor for Some Novel Pyrazolo[1,5-a]Pyrimidines and Tetraheterocyclic Compounds

The 2-(cyanomethyl)-5,7-dimethylpyrazolo[1,5-a]pyrimidine-3-carbonitrile 3 reacted with phenyl isothiocyanate to afford the respective thioanilide derivative 4 that is a novel compound that has been unreported hitherto. The latter was used as a precursor to synthesize several novel polyheterocyclic compounds 9, 12, 15, and 19. Treatment of the enamine derivative of compound 3 with each of hydrazine hydrate and hydroxylamine hydrochloride yielded the tetraheterocyclic compounds 22 and 23, respectively. The structures of all the newly synthesized compounds were confirmed on basis of their elemental, spectral data, and plausible mechanism has been postulated to account for their formation. X-ray crystallography was carried out as a further evidence for the structure of the isolated product 19.

Synthesis, Characterization and in vitro Antibacterial Evaluation of New Oxindoles and Spiro-Oxindoles Derivatives

A RYLIDENES oxindole 3 and 5 were synthesized via the reactions of isatin 1 with malononitrile dimmer 2 and 5-amino-3-(cyanomethyl)-1H-pyrazole-4-carbonitrile 4. Compound 3 react by Michael addition with malononitrile, ethyl 2-cyanoacetate and acetyl acet