Issue 24, 2009

Efficient one-pot synthesis of 2,4-di(het)aryl and 2,4-diamino pyrido[3,2-d]pyrimidines involving regioselective SNAr and palladium-catalyzed reactions

Abstract

An efficient and original synthesis of various 2,4-disubstituted pyrido[3,2-d]pyrimidines is reported. One-pot di(het)arylation and diamination approaches were used to obtain highly functionalized products in very good yields. The two one-pot processes were compared to their step-by-step related synthesis. Both routes started from 2,4-dichloropyrido[3,2-d]pyrimidine 1 and included a chlorine discrimination during the first reaction.

Graphical abstract: Efficient one-pot synthesis of 2,4-di(het)aryl and 2,4-diamino pyrido[3,2-d]pyrimidines involving regioselective SNAr and palladium-catalyzed reactions

Supplementary files

Article information

Article type
Paper
Submitted
09 Jul 2009
Accepted
10 Sep 2009
First published
15 Oct 2009

Org. Biomol. Chem., 2009,7, 5113-5118

Efficient one-pot synthesis of 2,4-di(het)aryl and 2,4-diamino pyrido[3,2-d]pyrimidines involving regioselective SNAr and palladium-catalyzed reactions

A. Tikad, S. Routier, M. Akssira and G. Guillaumet, Org. Biomol. Chem., 2009, 7, 5113 DOI: 10.1039/B913657F

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