Solid-phase synthesis of larger peptides by a new strategy of detachment from the resin

Attachment of the side‐chain carboxyl of the protected aspartic or glutamic acid ester to the resin support has been established for the solid‐phase synthesis of the asparagine or glutamine peptide. After further elongation of the α‐amino deprotected resin‐bound peptide ester with protected peptide fragments and the final detachment from the resin support by ammonolysis, the larger peptides containing, or preferably C‐terminated with, asparagine or glutamine could be obtained. Thus, the C‐peptide of human proinsulin was prepared by coupling to the resin‐bound dipeptide derivative, Leu‐Glu(OCH2Ph®)·OtBu, with six fragments consecutively. It was obtained in an overall yield of 36% after detaching from the resin with alcoholic ammonia, followed by mild acidolysis, DEAE cellulose chromatography, and gel filtration. This procedure has now been applied to the synthesis of the C‐terminal fragment of the insulin A chain ending in asparagine, and also to the synthesis of the threonine or serine peptide, where the anchorage to the resin was designed by the reaction of the sidechain hydroxyl with succinic anhydride in the presence of 4‐dimethylaminopyridine to form the hemiester of succinic acid, which in turn was condensed to the aminomethyl resin by the DCC‐HOBt procedure. Model experiments on the synthesis of the Z‐Thr(CO‐CH2CH2CONHCH2Ph®)·OtBu and Bpoc‐Lys(Boc)‐Thr(COCH2CH2CONHCH2Ph®)·OtBu, as well as their detachment from the resin by amminolysis or hydrazinolysis, have shown the potential for a milder process in the solid‐phase synthesis of larger peptides.