Most of the compounds have physiologically active properties, and their biological properties are often attributed to the heteroatoms contained in their molecules, and most of these heteroatoms also appear in cyclic structures. A Journal, Bulletin of the Korean Chemical Society called Microwave-assisted Transition Metal-catalyzed Coupling Approach to Indazole Diversity, Author is Oh, Yoo Jin; Yum, Eul Kgun, which mentions a compound: 651780-02-8, SMILESS is CC(C)(C)OC(=O)N1N=CC2=CC(Br)=CC=C12, Molecular C12H13BrN2O2, Reference of tert-Butyl 5-bromo-1H-indazole-1-carboxylate.
Diverse mono or biaryl substituents were introduced to indazole moieties under microwave-assisted palladium-catalyzed coupling reactions with isomeric bromoindazoles and aryl boronic acids. 1,3-Disubstituted indazoles were also obtained by C=C or C-N coupling of monosubstituted indazoles with functionalized terminal alkenes and arylhalides. Facile introduction of diverse substituents to indazoles showed useful synthetic approach for creating indazole compound library to discover biol. active small mols.
Compound(651780-02-8)Reference of tert-Butyl 5-bromo-1H-indazole-1-carboxylate received a lot of attention, and I have introduced some compounds in other articles, similar to this compound(tert-Butyl 5-bromo-1H-indazole-1-carboxylate), if you are interested, you can check out my other related articles.
Reference:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts