A new simple approach to the synthesis of unsymmetrical ureas HetNC(O)NRR′ (HetNH = pyrrole, indole, carbazole; R, R′ = H, alkyl, aryl) has been explored, which involves the direct reaction of the N-phenoxycarbonyl derivatives of pyrrole, indole and carbazole, HetNCO2Ph, with amines. The aminolysis reaction can be catalyzed by the amidine base DBU (1,8-diazabicyclo[5.4.0]undec-7-ene) under usually very mild conditions and provides a straightforward convenient entry into the target products through a route which avoids the traditional protocols based on multistep procedures and toxic phosgene or phosgene-derivatives.
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Carafa et al. (2011) studied this question.
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