514195-42-7Relevant articles and documents
Reductive amination of quinoline N-oxide with aminopyridines and their N-tozyl derivatives
Solekhova,Kurbatov
, p. 1192 - 1194 (2002)
In reaction of quinoline N-oxide with 2-aminopyridine in the presence of tosyl chloride the substrate undergoes reductive amination into 2-pyridyl(2-quinolyl)amine, and with 3- and 4-aminopyridines reductive tosylamination occurs to furnish N-tosyl derivatives of the corresponding 3- and 4-pyridyl(2-quinolyl)amines. N-tosyl derivatives of aminopyridines also react along reductive tosylamination pathway.