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Published on: May 15, 2012
A Novel Hydrazine Linker Resin and Its Application for the Solid-Phase Synthesis of alpha-Branched Primary Amines
1RWTH Aachen, Institut für Organische Chemie, Professor-Pirlet-Strasse 1, 52074 Aachen, Germany.
Abstract:
A novel hydrazine linker resin for solid-phase organic synthesis has been developed. Starting from Merrifield resin, the new N-butyl-N-methylpolystyrene-hydrazine linker is prepared in three steps. Polymer-supported hydrazones, readily prepared from aldehydes and the hydrazine resin, react with alkyl- and arylorganolithium reagents under 1,2-addition to the C-N double bond to afford the corresponding hydrazines. Release from solid support was achieved by reductive N-N bond cleavage using the borane-tetrahydrofuran complex. The resulting alpha-branched primary amines were protected as their amides or carbamates, respectively, and, after purification, were obtained in good overall yields and in high purity (12 examples).
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