Synthesis 2009(12): 1987-1990  
DOI: 10.1055/s-0029-1216784
PAPER
© Georg Thieme Verlag Stuttgart ˙ New York

Synthesis of Novel Trisubstituted Imidazolines

Frederick J. Lakner, Matthew A. Parker, Boris Rogovoy, Alexander Khvat*, Alexander Ivachtchenko
Department of Chemistry, ChemDiv Inc, 6605 Nancy Ridge Dr., San Diego, CA 92121, USA
Fax: +1(858)7944931; e-Mail: AK@chemdiv.com;
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Publikationsverlauf

Received 12 December 2008
Publikationsdatum:
27. April 2009 (online)

Abstract

Imidazolines substituted at the 1- and either the 4-, or 5-position with phenyl and at the 2-position with alkyl or phenyl have been prepared in racemic form. They appear to be fairly stable compounds and potentially useful as scaffolds in medicinal chemistry.

2

Evidence for acyl migration comes mainly from ¹H NMR spectra of isolated 6. In particular, two broad singlets of D2O-exchangeable protons were observed rather than the one singlet integrating to 2 H expected for amide 8.