Büllesbach E E, Naithani V K
Hoppe Seylers Z Physiol Chem. 1980 May;361(5):723-34.
Nepsilon 29, Nepsilon 59-Bis(methylsulfonylethoxycarbonyl)proinsulin was prepared from native beef proinsulin for its possible use in the semisynthesis of preproinsulin. The modification was made possible by first protecting the alpha-amino group of proinsulin either with the tert-butoxycarbonyl group, after reaction with bis(tert-butoxycarbonyl)oxide, or with the citraconyl group, after reaction with citraconic anhydride. Whereas Nalpha 1-tert-butoxycarbonylproinsulin was achieved by direct alkoxycarbonylation, Nalpha 1-citraconylproinsulin was obtained from partial deprotection of the quantitatively acylated proinsulin. The Nalpha 1-protected proinsulin derivatives were further quantitatively reacted with N-(methylsulphonylethoxycarbonyloxy)succinimide. The tert-butoxycarbonyl group was next removed by treatment with trifluoroacetic acid, or the citraconyl group removed by mild acid (pH 2.2) treatment. The resulting Nepsilon 29, Nepsilon 59-bis(methylsulphonylethoxycarbonyl)proinsulin was used in model reactions with the mixed anhydride of tert-butoxycarbonylmethionine with the aim of standardizing the coupling conditions to be used in the eventual synthesis of preproinsulin.
