Interrupted Intramolecular Hydroaminomethylation of <i>N</i>-Protected-2-vinyl Anilines: Novel Access to 3-Substitued Indoles or Indoline-2-ols
Frank Hochberger-Roa,
Perla H. García-Ríos,
José G. López-Cortés,
M. Carmen Ortega-Alfaro,
Jean-Claude Daran,
Maryse Gouygou,
Martine Urrutigoïty
Affiliations
Frank Hochberger-Roa
Laboratoire de Chimie de Coordination (LCC), Centre National de la Recherche Scientifique, Université de Toulouse, 31030 Toulouse, France
Perla H. García-Ríos
Laboratoire de Chimie de Coordination (LCC), Centre National de la Recherche Scientifique, Université de Toulouse, 31030 Toulouse, France
José G. López-Cortés
Instituto de Química, Universidad Nacional Autónoma de México, Circuito Exterior, Ciudad Universitaria, Coyoacán C.P., Ciudad de Mexico 04510, Mexico
M. Carmen Ortega-Alfaro
Instituto de Ciencias Nucleares, Universidad Nacional Autónoma de México, Circuito Exterior, Ciudad Universitaria, Coyoacán C.P., Ciudad de Mexico 04510, Mexico
Jean-Claude Daran
Laboratoire de Chimie de Coordination (LCC), Centre National de la Recherche Scientifique, Université de Toulouse, 31030 Toulouse, France
Maryse Gouygou
Laboratoire de Chimie de Coordination (LCC), Centre National de la Recherche Scientifique, Université de Toulouse, 31030 Toulouse, France
Martine Urrutigoïty
Laboratoire de Chimie de Coordination (LCC), Centre National de la Recherche Scientifique, Université de Toulouse, 31030 Toulouse, France
A new synthetic alternative to the synthesis of 3-methyl indoles and 3-methyl indoline-2-ols with an excellent atomic economy is presented in this study. It is demonstrated that the intramolecular interrupted hydroaminomethylation (HAM) reaction is a powerful tool for the formation of these compounds, which exhibit wide-ranging biological activity. Several N-Protected-2-vinyl anilines were synthesized and involved in the reaction producing the corresponding 3-methylindole or 3-methyl indoline-2-ol depending on the nature of the N-protecting groups.