
The CuCl2-mediated protocol was extended to the synthesis of 3,3-disubstituted aza-oxindoles. Compounds containing the aza-oxindole structural motif exhibit biological activities such as oral anti-inflammatory activity, and potent TrkA kinase and JAK 3 kinase inhibition. This article discusses the synthesis of 1,3-dimethyl-3-(p-tolyl)-1H-pyrrolo[3, 2-c]pyridine-2,(3H)-one by Cu(II)-mediated direct oxidative coupling. Keywords: N-Methyl-N-(pyridin-4-yl)-2-(p-tolyl)propanamide, 1,3-Dimethyl-3-(p-tolyl)-1H-pyrrolo[3,2-c]pyridin-2(3H)-one, CH coupling reaction, CuCl2 mediated aza-oxindole synthesis
540, ddc: ddc:540
540, ddc: ddc:540
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