Volume 29, Issue 1
Heterocyclic Compounds
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ChemInform Abstract: Alkylation of an Imidazolidine Enaminoester: A New Sequence for the Cα-Alkylation of 4,5-Dihydroimidazoles.

R. C. F. JONES

R. C. F. JONES

Dep. Chem., Open Univ., Milton Keynes MK7 6AA, UK

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P. PATEL

P. PATEL

Dep. Chem., Open Univ., Milton Keynes MK7 6AA, UK

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S. C. HIRST

S. C. HIRST

Dep. Chem., Open Univ., Milton Keynes MK7 6AA, UK

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I. TURNER

I. TURNER

Dep. Chem., Open Univ., Milton Keynes MK7 6AA, UK

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First published: 24 June 2010

Abstract

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ChemInform Abstract

Basic treatment of the enaminoester (I) with halogenoalkanes and epoxides successfully leads to C-alkylated products. Subsequent removal of the ester group offers a new route to 2-alkylated 4,5-dihydroimidazoles. With 1,3-dihalogenoalkanes C,N-dialkylation takes place yielding imidazopyridines like (X) efficiently.

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