Synthesis of 3-tetrazolylmethyl-azepino[4,5-b]indol-4-ones in two reaction steps: (Ugi-azide/N-acylation/SN2)/free radical cyclization and docking studies to a 5-Ht(6) model.

نویسندگان

  • Raul E Gordillo-Cruz
  • Angel Rentería-Gómez
  • Alejandro Islas-Jácome
  • Carlos J Cortes-García
  • Erik Díaz-Cervantes
  • Juvencio Robles
  • Rocío Gámez-Montaño
چکیده

A series of nine novel 3-tetrazolylmethyl-azepino[4,5-b]indol-4-ones were prepared in moderate to good overall yields in only two reaction steps. The first step consisted of a one-pot sequential process of an Ugi-azide multicomponent reaction, N-acylation and SN2 to give the xanthates. The second step was an intramolecular cyclization under free radical conditions. Also, their binding modes have been modelled using docking techniques.

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عنوان ژورنال:
  • Organic & biomolecular chemistry

دوره 11 38  شماره 

صفحات  -

تاریخ انتشار 2013