Process for the manufacture of persilylated peptides
Process for the manufacture of a peptide or peptide analog, which comprises (a) producing a persilylated peptide or persilylated peptide analogue by silylating a corresponding peptide by reaction with a silylating agent other than trimethylsilylcyanide, and (b) reacting a compound of formula (I) X-A-COOH wherein X is an amino protecting group, A is an amino acid, peptide or peptide analogue residue, and —COOH designates an optionally activated carboxylic group, with a persilylated peptide or a persilylated peptide analogue containing from 4 to 15 amino acids.
1. A process for the manufacture of a peptide or peptide analogue, which comprises (a) producing a persilylated peptide or persilylated peptide analogue containing from 4 to 15 amino acids by silylating a corresponding peptide by reaction with a silylating agent other than trimethylsilylcyanide; and (b) reacting a compound of formula (I) X-A-COOH, wherein X is an amino protecting group, A is an amino acid, peptide or peptide analogue residue, and —COOH designates an optionally activated carboxylic group, with the persilylated peptide or persilylated peptide analogue of step (a).
2. The process according to claim 1 , wherein the persilylated peptide contains 4, 5, 6, 7, or 8 amino acids.
3. The process according to claim 1 , wherein the reaction of step (a) is carried out in an organic solvent.
4. The process according to claim 1 , wherein the silylating agent is N-methyl-N-trimethylsilylacetamide (MSA).
5. The process according to claim 3 wherein the organic solvent is N,N-dimethylacetamide (DMAC).
6. The process according to claim 1 , wherein 0.7 to 1.5 equivalents of silylating agent are used relative to the molar amount of functional groups to be silylated.
7. The process according to claim 1 , wherein A comprises 2, 3, 4, 5, 6, 7, 8 or 9 amino acids.
8. The process according to claim 1 , wherein X is an electron-withdrawing amino protecting group.
9. The process according to claim 8 , wherein X is a t-butoxycarbonyl group.
10. The process according to claim 1 , wherein the reaction of step (b) is carried out in the presence of a carboxyl group activating agent selected from the group consisting of pivaloyl chloride and isobutyl chloroformate.
11. The process according to claim 1 further comprising removing the group X from the compound produced by the reaction.
12. The process according to claim 4 , wherein the reaction of step (a) is carried out in an organic solvent which is N,N-dimethylacetamide (DMAC).