Synthesis and application of N(\u00ce\u00b1) -Fmoc-N(\u00cf\u20ac) -4-methoxybenzyloxymethylhistidine in solid phase peptide synthesis.
Hibino H, Miki Y, Nishiuchi Y.
J Pept Sci. 2012 Oct 30. doi: 10.1002\/psc.2464. [Epub ahead of print]<\/p>\n
The 4-methoxybenzyloxymethyl (MBom) group was introduced at the N(\u00cf\u20ac) -position of the histidine (His) residue by using a regioselective procedure, and its utility was examined under standard conditions used for the conventional and the microwave (MW)-assisted solid phase peptide synthesis (SPPS) with 9-fluorenylmethyoxycarbonyl (Fmoc) chemistry. The N(\u00cf\u20ac) -MBom group fulfilling the requirements for the Fmoc strategy was found to prevent side-chain-induced racemization during incorporation of the His residue even in the case of MW-assisted SPPS performed at a high temperature. In particular, the MBom group proved to be a suitable protecting group for the convergent synthesis because it remains attached to the imidazole ring during detachment of the protected His-containing peptide segments from acid-sensitive linkers by treatment with a weak acid such as 1% trifluoroacetic acid in dichloromethane. We also demonstrated the facile synthesis of Fmoc-His(\u00cf\u20ac-MBom)-OH with the aid of purification procedure by crystallization to effectively remove the undesired \u00cf\u201e-isomer without resorting to silica gel column chromatography. This means that the present synthetic procedure can be used for large-scale production without any obstacles. Copyright \u00a9 2012 European Peptide Society and John Wiley & Sons, Ltd.<\/p>\n