Abstract

The optimization of a Ugi reaction involving the mixing of furfurylamine, benzaldehyde, boc-glycine and t-butylisocyanide is described. Triplicate runs of 48 parallel experiments are reported, varying concentration, solvent and the excess of some of the reagents. The isolation of the product was achieved by a simple filtration and wash procedure. The highest yield obtained was 66% from 0.4 M methanol with 1.2 eq. of imine. This is significantly above the 49% yield obtained from the initial reaction under equimolar concentration at 0.4 M in methanol. Methanol solutions with reagent concentrations of 0.4M or 0.2M gave superior yields while all solvent systems at 0.07M performed poorly. At 0.2M, methanol and ethanol/methanol (60/40) mixtures were statistically equally good while THF/methanol (60/40) was poor and acetonitrile/methanol (60/40) was intermediate. Good reproducibility of the precipitate yields was obtained in these replicate experiments, allowing for subtle interaction effects to be positively identified.

Highlights

  • The Ugi reaction has proved to be a convenient way to quickly create diverse libraries of compounds [1,2,3]

  • It has been observed that Ugi products sometimes precipitate in pure form from the reaction mixture [1,5]

  • A single factor analysis of variance (ANOVA) indicates a significant difference in average yield for the four solvents studied at a reagent concentration of 0.2M

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Summary

Introduction

The Ugi reaction has proved to be a convenient way to quickly create diverse libraries of compounds [1,2,3]. It would be most beneficial to optimize the Ugi product yield as obtained directly from filtering the reaction mixture without further treatment.

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