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Merck

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

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

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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Sigma-Aldrich
クロロ-(2-ジシクロヘキシルホスフィノ-2′,6′-ジイソプロポキシ-1,1′-ビフェニル)[2-(2-アミノエチル)フェニル]パラジウム(II)-メチル-t-ブチルエーテル付加物, 95%