Susceptibility of Methyl 3-Amino-1 H-pyrazole-5-carboxylate to Acylation

A Kusakiewicz-Dawid, Ł Górecki…

Index: Kusakiewicz-Dawid, Anna; Gorecki, Lukasz; Masiukiewicz, Elzbieta; Rzeszotarska, Barbara Synthetic Communications, 2009 , vol. 39, # 22 p. 4122 - 4132

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Abstract

Abstract In the search for a new method of synthesis of hybrid peptides with aminopyrazole carboxylic acid, we tried to force selective acylation at the aromatic amino group instead of at the ring nitrogen atom with fairly gentle acylating agents. The acylating agents used were acid anhydrides: acetic anhydride, tert-butyl pyrocarbonate, and 2-(2-methoxyethoxy) ethoxyacetic acid/dicyclohexylcarbodiimide. We succceded in acylation at this amino ...

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