Trautwein A W, Süssmuth R D, Jung G
Institut für Organische Chemie, Eberhard-Karls-Universität Tübingen, Germany.
Bioorg Med Chem Lett. 1998 Sep 8;8(17):2381-4. doi: 10.1016/s0960-894x(98)00430-2.
An efficient method for solid-phase synthesis of pyrroles is described. Polystyrene Rink amide resin is acetoacetylated and converted into polymer bound enaminones upon treatment with primary amines. These then undergo a Hantzsch reaction with alpha-bromoketones to yield pyrroles. After cleavage with 20% trifluoroacetic acid in dichloromethane pyrrole-3-carboxamides are obtained in excellent purity.