Synthesis 2015; 47(23): 3767-3775
DOI: 10.1055/s-0035-1560456
paper
© Georg Thieme Verlag Stuttgart · New York

Synthesis of Heteroaryl ortho-Phenoxyethylamines via Suzuki Cross-Coupling: Easy Access to New Potential Scaffolds in Medicinal Chemistry

Leda Ivanova Manasieva
Dipartimento di Scienze della Vita, Università di Modena e Reggio Emilia, Via Campi 103, 41125 Modena, Italy   Email: silvia.franchini@unimore.it
,
Battisti Umberto Maria
Dipartimento di Scienze della Vita, Università di Modena e Reggio Emilia, Via Campi 103, 41125 Modena, Italy   Email: silvia.franchini@unimore.it
,
Adolfo Prandi
Dipartimento di Scienze della Vita, Università di Modena e Reggio Emilia, Via Campi 103, 41125 Modena, Italy   Email: silvia.franchini@unimore.it
,
Livio Brasili
Dipartimento di Scienze della Vita, Università di Modena e Reggio Emilia, Via Campi 103, 41125 Modena, Italy   Email: silvia.franchini@unimore.it
,
Silvia Franchini*
Dipartimento di Scienze della Vita, Università di Modena e Reggio Emilia, Via Campi 103, 41125 Modena, Italy   Email: silvia.franchini@unimore.it
› Author Affiliations
Further Information

Publication History

Received: 06 May 2015

Accepted after revision: 16 July 2015

Publication Date:
01 September 2015 (online)


Abstract

Heteroaryl ortho-phenoxyethylamines have been extensively employed in medicinal chemistry as privileged scaffolds for the design of highly potent and selective ligands. Herein an efficient, fast, and general method for the synthesis of heteroaryl phenoxyethylamines via Suzuki­ cross-coupling is reported. This approach offers the opportunity to obtain a large variety of biaryls incorporating five-membered (thiophene, furan, thiazole, pyrazole, imidazole) or six-membered (pyridine, pyrimidine) heteroaromatic rings for appropriate libraries of ligands. All the compounds presented here have never been synthesized before and a full structural characterization is given.

 
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