Issue 8, 2012

Synthesis of substituted pyrazolo[4,3-b]pyridines via copper-mediated intramolecular C–N cross-coupling of primary allylamines

Abstract

Copper-catalyzed intramolecular amination followed by in situ oxidation of primary allylamines generated from the Morita–Baylis–Hillman adducts of 4-iodopyrazolecarbaldehydes for preparing substituted pyrazolo[4,3-b]pyridines is described. The synthetic methodology is versatile and is not affected by the stereochemistry of the allylamine. In contrast, similar coupling reactions employing secondary allylamines as the starting material were unsuccessful.

Graphical abstract: Synthesis of substituted pyrazolo[4,3-b]pyridines via copper-mediated intramolecular C–N cross-coupling of primary allylamines

Supplementary files

Article information

Article type
Paper
Submitted
23 Nov 2011
Accepted
20 Jan 2012
First published
27 Feb 2012

RSC Adv., 2012,2, 3367-3373

Synthesis of substituted pyrazolo[4,3-b]pyridines via copper-mediated intramolecular C–N cross-coupling of primary allylamines

M. Nayak and S. Batra, RSC Adv., 2012, 2, 3367 DOI: 10.1039/C2RA01170K

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