The synthesis of a di-nor-secorhazinilam analogue is described. This phenylpyrrole compound has been prepared by a Susuki cross-coupling reaction between 1,2,5 trisubstituted pyrrole halides and 2-N-(tert-butoxycarbonyl)aminophenyl boronic acid. In contrast to rhazinilam, this new phenylpyrrole inhibits the assembly of tubulin into microtubules.