Synthesis of acylic derivatives of prolylleucylglycinamide
https://doi.org/10.29235/1561-8331-2019-55-4-429-435
Abstract
Tert-butyloxycarbonylprolylleucylglycinamide is obtained both by the interaction of tert-butyloxycarbonylprol ylleucylglycine ethyl ester with a methanolic ammonia solution and by the reaction of glycine amide with a mixed anhydride which was synthesized from tert-butyloxycarbonylprolylleucine and isobutylchloroformate. The removal of the tert-butyloxycarbonyl group by the action of formic acid or a dioxane solution of hydrogen chloride and treatment of the resulting salts with the corresponding base yielded a prolylleucylglycinamide, by the interaction of which with acetic, benzoic or 5-phenylisoxazole-3-carboxylic acids chlorides acyl derivatives of prolylleucylglycinamide are obtained.
About the Authors
V. A. HaidukevichBelarus
Veranika A. Haidukevich – Junior Researcher.
13, Surganov Str., 220072, Minsk
S. K. Petkevich
Belarus
Sergey K. Petkevich – Ph. D. (Chemistry), Leading Researcher.
13, Surganov Str., 220072, Minsk
E. G. Karankevich
Belarus
Helen G. Karankevich – Ph. D. (Chemistry), Head of the Laboratory.
13, Surganov Str., 220072, Minsk
P. V. Kurman
Belarus
Peter V. Kurman – Ph. D. (Chemistry), Leading Researcher.
5/2, Academician V. F. Kuprevich Str., 220141, Minsk
Z. I. Kuvaeva
Belarus
Zoya I. Kuvaeva – D. Sc. (Chemistry), Professor, Head of the Department.
13, Surganov Str., 220072, Minsk
V. I. Potkin
Belarus
Vladimir I. Potkin – Сorresponding Member of the National Academy of Sciences of Belarus, D. Sc. (Chemistry), Professor, Head of the Department.
13, Surganov Str., 220072, Minsk
V. A. Knizhnikov
Belarus
Valeriy A. Knizhnikov – D. Sc. (Chemistry), Head of the Laboratory.
13, Surganov Str., 220072, Minsk
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