Synthesis 2016; 48(02): 256-262
DOI: 10.1055/s-0035-1560392
paper
© Georg Thieme Verlag Stuttgart · New York

A Novel Convenient Synthesis of Pyridinyl and Quinolinyl Triflates and Tosylates via One-Pot Diazotization of Aminopyridines and Aminoquinolines in Solution

Autoren

  • Assiya Zh. Kassanova

    Department of Biotechnology and Organic Chemistry, National Research Tomsk Polytechnic University, 634050 Tomsk, Russian Federation   eMail: eak@tpu.ru   eMail: filimonov@tpu.ru
  • Elena A. Krasnokutskaya*

    Department of Biotechnology and Organic Chemistry, National Research Tomsk Polytechnic University, 634050 Tomsk, Russian Federation   eMail: eak@tpu.ru   eMail: filimonov@tpu.ru
  • Perizat S. Beisembai

    Department of Biotechnology and Organic Chemistry, National Research Tomsk Polytechnic University, 634050 Tomsk, Russian Federation   eMail: eak@tpu.ru   eMail: filimonov@tpu.ru
  • Victor D. Filimonov*

    Department of Biotechnology and Organic Chemistry, National Research Tomsk Polytechnic University, 634050 Tomsk, Russian Federation   eMail: eak@tpu.ru   eMail: filimonov@tpu.ru
Weitere Informationen

Publikationsverlauf

Received: 01. Oktober 2015

Accepted after revision: 04. November 2015

Publikationsdatum:
02. Dezember 2015 (online)


Graphical Abstract

Abstract

The first effective and simple method for the direct one-pot transformation of 2-, 3-, and 4-aminopyridines, 2,6-diaminopyridines, and 2-aminoquinoline into the corresponding pyridinyl and quinolinyl trifluoromethanesulfonates and tosylates in solvents was developed. The procedure involves diazotization of the heterocyclic amines with sodium nitrite in mixed hexane–DMSO or hexane–DMF solutions in the presence of trifluoromethanesulfonic acid or p-toluenesulfonic acid.

Supporting Information