First Practical Synthesis of Formamidine Ureas and Derivatives
journal contributionposted on 29.03.2003 by Amy S. Ripka, David D. Díaz, K. Barry Sharpless, M. G. Finn
Any type of content formally published in an academic journal, usually following a peer-review process.
Isonitriles and ureas undergo a condensation reaction in the presence of acid chlorides to give formamidine ureas, for which no general synthetic routes currently exist. A mechanism is proposed in which the key intermediate is an electrophilic adduct of isonitrile and acid chloride. The process is tolerant of moderate variability in the nature of the components, and access to formamidine ureas of varying substitution patterns is further enhanced by a facile exchange reaction with amines.