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Tandem copper (Cu) catalysed N-arylation-vinylogous nitroaldol condensation of 3,5-disubstituted 4-nitropyrazoles.

Organic & biomolecular chemistry (2015-07-03)
Owk Obulesu, Jagadeesh Babu Nanubolu, Surisetti Suresh
RÉSUMÉ

A tandem process involving copper catalysed N-arylation and vinylogous nitroaldol condensation is described. The reaction of 3,5-dialkyl substituted 4-nitropyrazoles and ortho-halo substituted (hetero)aryl aldehydes or ketones furnished 3-nitropyrazolo[1,5-a]quinoline and heteroaryl-fused 3-nitropyrazolo[1,5-a]pyridine derivatives in moderate to high yields.

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Sigma-Aldrich
Iode, ≥99.99% trace metals basis
Sigma-Aldrich
Iode, 99.999% trace metals basis
Sigma-Aldrich
Iode, anhydrous, beads, −10 mesh, 99.999% trace metals basis