53226-29-2

Usage

Molecular structure

A chemical compound consisting of a pentofuranosyl group (a five-carbon sugar molecule) attached to a 1H-pyrazolo[3,4-b]pyrazine ring system.

Type of compound

A heterocyclic compound.

Pharmaceutical applications

Has potential pharmaceutical applications due to its unique structure and properties.

Sugar group

The presence of the sugar group in its structure suggests that it may have potential as a nucleoside analog or as a molecular probe for studying interactions with biological systems.

Specific chemical and biological properties

Its specific chemical and biological properties make it an interesting target for further research and potential development as a pharmaceutical agent.

Upstream product

• 53226-27-0 tri-O-acetyl-1-pyrazolo[3,4-b]pyrazin-1-yl-β-D-1-deoxy-ribofuranose 
• 55726-11-9 ethyl 5-amino-1-(2,3-O-isopropylidene-β-D-ribofuranosyl)-1H-pyrazole-4-carboxylate 
• 716379-20-3 5-amino-4-benzyloxycarbonylamino-1-(2,3,5-tri-O-acetyl-β-D-ribofuranosyl)pyrazole 
• 716379-17-8 5-amino-1-(2,3-O-isopropylidene-β-D-ribofuranosyl)pyrazole-4-carbonylazide 
• 716379-18-9 Acetic acid (2R,3R,4R,5R)-4-acetoxy-5-acetoxymethyl-2-(5-amino-4-azidocarbonyl-pyrazol-1-yl)-tetrahydro-furan-3-yl ester 
• 716379-16-7 5-Amino-1-((3aR,4R,6R,6aR)-6-hydroxymethyl-2,2-dimethyl-tetrahydro-furo[3,4-d][1,3]dioxol-4-yl)-1H-pyrazole-4-carboxylic acid hydrazide 

Relevant academic research and scientific papers

Facile synthesis of 1-substituted 4,5-diaminopyrazoles and its application toward the synthesis of pyrazolo[3,4-b]pyrazines

1-Substituted 5-aminopyrazole-4-carbonylazides were prepared from the appropriate 5-aminopyrazole-4-carboxylates. The acyl azides undergo a Curtius rearrangement followed by quenching with alcohols to form the corresponding carbamates. The 1-substituted 5