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Palladium-catalyzed amination of unprotected halo-7-azaindoles.

Organic letters (2010-09-24)
Jaclyn L Henderson, Sarah M McDermott, Stephen L Buchwald
ZUSAMMENFASSUNG

Simple and efficient procedures for the Pd-catalyzed cross-coupling of primary and secondary amines with halo-7-azaindoles(pyrrolo[2,3-b]pyridine) are presented. Previously, no general method was available to ensure the highly selective reaction of the heteroaryl halide in the presence of the unprotected azaindole N-H. Using palladium precatalysts recently reported by our group, such reactions are easily accomplished under mild conditions that can be applied to cross-coupling reactions with a wide array of aliphatic and aromatic amines.

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Produktbeschreibung

Sigma-Aldrich
(2-Dicyclohexylphosphino-2′,6′-diisopropyl-1,1′-biphenyl)[2-(2-aminoethyl)-phenyl)]-palladium(II), 95%