332875-32-8

Upstream product

• 77-78-1 dimethyl sulfate 
• 55052-24-9 1H-Pyrrolo[2,3-b]pyridine-7-oxide 
• 27257-15-4 1-methyl-1H-pyrrolo[2,3-b]pyridine 

Downstream Products

• 1128075-61-5 6-(4-methoxyphenyl)-1-methyl-1H-pyrrolo[2,3-b]pyridine 7-oxide 
• 1128075-60-4 1-methyl-6-p-tolyl-1H-pyrrolo[2,3-b]pyridine 7-oxide 
• 1128075-68-2 1-methyl-2-p-tolyl-1H-pyrrolo[2,3-b]pyridine 7-oxide 
• 1128075-69-3 1-methyl-2,6-di-p-tolyl-1H-pyrrolo[2,3-b]pyridine 7-oxide 
• 1128075-67-1 1-methyl-6-o-tolyl-1H-pyrrolo[2,3-b]pyridine 7-oxide 
• 1128075-63-7 6-(4-(methoxycarbonyl)phenyl)-1-methyl-1H-pyrrolo[2,3-b]pyridine 7-oxide 
• 1128075-64-8 1-methyl-6-(4-(trifluoromethyl)phenyl)-1H-pyrrolo[2,3-b]pyridine 7-oxide 
• 1128075-62-6 1-methyl-6-(1-tosyl-1H-indol-5-yl)-1H-pyrrolo[2,3-b]pyridine 7-oxide 
• 1128075-66-0 6-(4-fluorophenyl)-1-methyl-1H-pyrrolo[2,3-b]pyridine 7-oxide 

Relevant academic research and scientific papers

Visible Light-Mediated Decarboxylative Alkylation of Pharmaceutically Relevant Heterocycles

A net redox-neutral method for the decarboxylative alkylation of heteroarenes using photoredox catalysis is reported. Additionally, this method features the use of simple, commercially available carboxylic acid derivatives as alkylating agents, enabling the facile alkylation of a variety of biologically relevant heterocyclic scaffolds under mild conditions.

Site-selective azaindole arylation at the azine and azole rings via N-oxide activation

Subjection of N-methyl 6-and 7-azaindole N-oxides to a Pd(OAc) 2/DavePhos catalyst system enables regioselective direct arylation of the azine ring. Following deoxygenation, 7-azaindole substrates undergo an additional regioselective azole direct arylation event in good yield.