Synthesis 2002(11): 1509-1512
DOI: 10.1055/s-2002-33338
PAPER
© Georg Thieme Verlag Stuttgart · New York

Preparation of 5-Heteroaryl Substituted 1-(4-Fluorophenyl)-1H-indoles via Palladium-Catalyzed Negishi and Stille Cross-Coupling Reactions

Thomas Ballea,b, Kim Andersen*a, Per Vedsøb,
a Department of Combinatorial Chemistry, H. Lundbeck A/S, Ottiliavej 9,2500 Valby, Denmark
Fax: +4536301385; e-Mail: kia@lundbeck.com;
b Department of Medicinal Chemistry, The Royal Danish School of Pharmacy, Universitetsparken 2,2100 Copenhagen, Denmark
Further Information

Publication History

Received 21 March 2002
Publication Date:
23 August 2002 (online)

Abstract

Palladium-catalyzed Negishi cross-coupling of 5-1-(4-fluorophenyl)indolylzinc chloride with N-methyl-halopyrazoles, bromopyridines and bromopyrimidines in gram scale gave the corresponding cross-coupled products in 38-85% yield.

1

Current address: Medicinal Chemistry Research, Novo Nordisk A/S, Novo Nordisk Park, 2760 Måløv, Denmark.

16

We performed Negishi cross-coupling reactions in 21 g (73 mmol) scale without encountering any problems. See preparation of 11.