Method of preparing multi-modal anion-exchange ligands
View Patent ↗The invention relates to a method of preparing multi-modal anion-exchange ligands, which comprises providing a cyclic three-functional scaffold comprising an amine, a carbonyl and a thiol; optionally derivatisation of the amine of the scaffold to provide an anion-exchanging group and/or to protect the amine; and aminolysis to open up the derivative by adding a reagent comprising an amine coupled to a residue R in order to add said amine to the carbonyl carbon of the opened scaffold. The scaffold is advantageously homocysteine thiolactone. In one embodiment, the method comprises an additional step of immobilising the opened scaffold to a base matrix to provide a separation medium, such as a chromatography medium.
1. A method of preparing at least one multi-modal anion-exchange ligand, which method comprises the steps of
(a) providing at least one scaffold defined by the general formula (I) below
wherein A, B and X irrespective of each other are carbon atoms or any heteroatoms, m is any integer between 0 and 4, and the functional group N is a nitrogen, which either replaces one X or is attached to any one of A, B and X;
(b) optionally derivatizing the nitrogen of the scaffold(s) to provide an anion-exchanging group and/or to protect the amine, while retaining the cyclic structure of the scaffold; and
(c) subjecting said scaffold to aminolysis to open up the cyclic structure of the resulting derivative by adding a reagent comprising an amine coupled to a residue R to add said amine to the carbonyl carbon of the opened scaffold.
2. The method of claim 1 , wherein in formula (I), A, B, and X are carbon atoms and m is 1.
3. The method of claim 1 , wherein the scaffold is homocysteine thiolactone.
4. The method of claim 1 , wherein step (b) is performed and the derivatisation of is an alkylation that provides a secondary, tertiary or quaternary amine.
5. The method of claim 1 , wherein the reagent added to provide the aminolysis of step (c) includes an amine coupled to a residue R, which R is selected from the group consisting of linear, branched, cyclic, saturated, unsaturated and aromatic hydrocarbon groups.
6. The method of claim 1 , wherein steps (a) and (b) have been performed earlier to provide a ready-derivatised scaffold.
7. The method of claim 1 , which further comprises a step (d) of immobilising the opened scaffold via the thiol group to a base matrix including a reactive group.
8. The method of claim 1 , which further comprises a step of brominating the reactive group of the base matrix, wherein said reactive group is a carbon-carbon double bond.
9. The method of claim 1 , which further comprises a step of activating the reactive group of the base matrix under conditions favouring radical reaction, wherein said reactive group is a carbon-carbon double bond.