389058-54-2

Basic information

• Product Name: 3-[3-(5-carbamoyl-1,3-dimethyl-1H-pyrazolo[3,4-b]pyridin-4-ylamino)-phenoxy]-pyrrolidine-1-carboxylic acid tert-butyl ester
• Synonyms: 3-[3-(5-carbamoyl-1,3-dimethyl-1H-pyrazolo[3,4-b]pyridin-4-ylamino)-phenoxy]-pyrrolidine-1-carboxylic acid tert-butyl ester
• CAS NO: 389058-54-2
• Molecular Weight: 466.54
• Mol File: 389058-54-2.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 3-[3-(5-carbamoyl-1,3-dimethyl-1H-pyrazolo[3,4-b]pyridin-4-ylamino)-phenoxy]-pyrrolidine-1-carboxylic acid tert-butyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: 3-[3-(5-carbamoyl-1,3-dimethyl-1H-pyrazolo[3,4-b]pyridin-4-ylamino)-phenoxy]-pyrrolidine-1-carboxylic acid tert-butyl ester(389058-54-2)
• EPA Substance Registry System: 3-[3-(5-carbamoyl-1,3-dimethyl-1H-pyrazolo[3,4-b]pyridin-4-ylamino)-phenoxy]-pyrrolidine-1-carboxylic acid tert-butyl ester(389058-54-2)

Safety Data

• Hazardous Substances Data: 389058-54-2(Hazardous Substances Data)

Upstream product

• 741290-77-7 tert-butyl (3S)-3-(3-nitrophenoxy)pyrrolidine-1-carboxylate 
• 175201-94-2 4-chloro-1,3-dimethyl-1H-pyrazolo[3,4-b]pyridine-5-carboxylic acid 
• 175201-95-3 4-Chloro-1,3-dimethyl-1H-pyrazolo[3,4-b]pyridine-5-carbonyl chloride 
• 20481-33-8 diethyl 2-{[(1,3-dimethyl-1H-pyrazol-5-yl)amino]methylene}malonate 
• 20481-15-6 ethyl 4-chloro-1,3-dimethylpyrazolo[3,4-b]pyridine-5-carboxylate 
• 109431-87-0 (R)-tert-butyl 3-hydroxypyrrolidine-1-carboxylate 
• 554-84-7 meta-nitrophenol 
• 3524-32-1 5-Amino-1,3-dimethylpyrazole 
• 175201-98-6 4-chloro-1,3-dimethyl-1H-pyrazolo[3,4-b]pyridine-5-carboxamide 
• 741290-82-4 tert-butyl (3S)-3-(3-aminophenoxy)pyrrolidine-1-carboxylate 

Downstream Products

• 389058-61-1 1,3-dimethyl-4-[3-(pyrrolidin-3-yloxy)-phenylamino]-1H-pyrazolo[3,4-b]pyridine-5-carboxylic acid amide 

Relevant articles and documents

New orally active PDE4 inhibitors with therapeutic potential

The design, synthesis, and biological evaluation of a series of pyrazolopyridines was carried out. Structural optimization of the aniline moiety of 4-anilinopyrazolopyridine derivative 3a, which is one of the newly discovered chemical leads for PDE4 inhib