Published in

Thieme Gruppe, Synthesis: Journal of Synthetic Organic Chemistry, 04(1995), p. 449-452, 1995

DOI: 10.1055/s-1995-3925

Links

Tools

Export citation

Search in Google Scholar

Preparation of Highly Functionalized Imidazoles from α- Azidoacetonitrile: X-Ray Crystal Structure of 4-Methoxy-2-methylamino- 5-methylthiocarbamoylimidazole

This paper is made freely available by the publisher.
This paper is made freely available by the publisher.

Full text: Download

Red circle
Preprint: archiving forbidden
Orange circle
Postprint: archiving restricted
Red circle
Published version: archiving forbidden
Data provided by SHERPA/RoMEO

Abstract

The Pinner salt 2 derived from alpha-azidoacetonitrile by sequential treatment with triethylamine, triphenylphosphine and acyl chlorides or isothiocyanates was converted into the corresponding imidazole 5 or 6, respectively. The crystal structure of 6a has been determined by X-ray diffraction methods. Dimers of centrosymmetrically related molecules, linked by N-H...N bonds, join together to infinite chains through N-H...S=C halogen interactions.