Coupling in the absence of tertiary amines

Abstract

In order to avoid base catalyzed side reactions during coupling, attempts were made to render superfluous the addition of tertiary amines to the reaction mixture. Weak acids were applied for the removal of acid labile protecting groups. Acetic acid and other carboxylic acids were considered unsuitable for this purpose because the resulting salts could be the cause of chain termination in the next coupling step. Pentachlorophenol and 2,4‐dinitrophenol cleaved the Bpoc, Nps and Trt groups but more practical rates were reached with solutions of 1‐hydroxybenzotriazole (HOBt) in trifluoroethanol, in acetic acid, or in a mixture of phenol and p‐cresol. In addition to acidolysis, HOBt salts of amino components could also be obtained through hydrogenolysis of the Z group or thiolysis of the Nps group in the presence of HOBt, or by the displacement of acetic acid from acetate salts with HOBt. Acylation of HOBt salts of amino components with symmetrical or mixed anhydrides or with active esters did not require the addition of tertiary amine. © 1982 Munksgaard, Copenhagen