Azide alkyne Huisgen cycloaddition

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The Azide-Alkyne Huisgen Cycloaddition is a 1,3-dipolar cycloaddition between an azide and a terminal or internal alkyne to give a 1,2,3-triazole. Huisgen ^[1] was the first to understand the scope of this organic reaction. This cycloaddition is considered the cream of the crop of click chemistry.

In the reaction above ^[2] azide 2 reacts neatly with alkyne 1 to afford the triazole 3 as a mixture of 1,4-adduct and 1,5-adduct at 98 °C in 18 hours.

[edit] Variants of the Huisgen reaction

A notable variant of the Huisgen 1,3-dipolar cycloaddition is the copper(I) catalyzed variant, in which organic azides and terminal alkynes are untied to afford 1,4-regioisomers of 1,2,3-triazoles as sole products. The copper(I)-catalyzed variant was first reported by Morten Meldal and co-workers at the Carlsberg Laboratory in Denmark. While the copper(I) catalyzed variant gives rise to a triazole from a terminal alkyne and an azide, formally it is not a 1,3-dipolar cycloaddition and thus should not be termed a Huisgen cycloaddition. This reaction is better termed the Copper(I)-catalyzed Azide-Alkyne Cycloaddition (CuAAC). But it is certainly a click reaction. While the reaction can be performed using commerical sources of copper(I) such as cuprous bromide or iodide, the reaction works much better using a mixture of copper(II) (e.g. copper(II) sulfate) and a reducing agent (e.g. sodium ascorbate) to produce Cu(I) in situ. As Cu(I) is unstable in aqueous solvents, stabilizing ligands are effective for improving the reaction outcome, especially if Tim's Ligand (TBTA) is used. Those organic chemists serious about success in running these reactions will prepare their own TBTA ligand. The reaction can be run in a variety of solvents, and mixtures of water and a variety of (partially) miscible organic solvents including alcohols, DMSO, DMF, tBuOH and acetone work well. Owing to the powerful coordinating ability of nitriles towards Cu(I) it is best to avoid acetonitrile as the solvent.

NH-1,2,3-triazoles are also prepared from alkynes in a sequence called the Banert cascade.

The utility of the Cu(I) catalyzed click reaction has also been demonstrated in the polymerization reaction of a bis-azide and a bis-alkyne with copper(I) and Tim's Ligand (TBTA) to a conjugated fluorene based polymer ^[3]. The degree of polymerization easily exceeds 50 and with a stopper molecule such as phenyl azide well defined phenyl end-groups are obtained.

The CuAAC click reaction also effectively couples polystyrene and bovine serum albumin (BSA) ^[4]. The result is an amphiphilic biohybrid. BSA contains a thiol group at Cys-34 which is functionalized with an alkyne group. Polystyrene has an azido end-group and the coupling takes place in a THF / phosphate buffer solution with Copper(II) sulfate and ascorbic acid. In water the biohybrid micelles with a diameter of 30 to 70 nanometer form aggregates.

[edit] References