2-(1-ADAMANTYL)-7-METHYLIMIDAZO[1,2-<i>a</i>]PYRIDINE AND ITS REACTIONS WITH N-BROMOSUCCINIMIDE

Authors

  • Р. И. Юрченко National Technical University of Ukraine, "Kiev Polytechnical Institute," Kiev
  • А. Д. Пономаренко National Technical University of Ukraine, "Kiev Polytechnical Institute," Kiev
  • Н. С. Савина National Technical University of Ukraine, "Kiev Polytechnical Institute," Kiev
  • А. А. Толмачев National Technical University of Ukraine, "Kiev Polytechnical Institute," Kiev

DOI:

https://doi.org/10.1007/8420

Keywords:

2-(1-adamantyl)-7-methylimidazo[1, 2-a]pyridine, N-bromosuccinimide, bromination

Abstract

In  reaction  with equimolar amount or twice the  amount of N-bromosuccinimide 2-(1-adamantyl)-7-methylimidazo[1,2-a]pyridine, obtained from 2-amino-4-methylpyridine and bromomethyl 1-adamantyl ketone, is converted into 2-(1-adamantyl)-3-bromo-7-methylimidazo[1,2-a]pyridine. With three times the amount of N-bromosuccinimide it gives 2-(1-adamantyl)-3-bromo-7-formylimidazo[1,2-a]pyridine.

How to Cite
Yurchenko, R. I.; Ponomarenko, A. D.; Savina, N. S.; Tolmachev, A. A.  Chem. Heterocycl. Compd. 2004, 40, 1543. [Khim. Geterotsikl. Soedin. 2004, 1791.]

For this article in the English edition, see DOI 10.1007/s10593-005-0096-5


Published

2023-12-08

Issue

Section

Original Papers