Chemistry of Heterocyclic Compounds

, Volume 8, Issue 11, pp 1406–1407 | Cite as

Synthesis and transformations of 2-(2-furyl)-and 2-[β;-(2-furyl)vinyl]naphth[1,2-d]imidazoles

  • L. Ya. Oleinikova
  • F. T. Pozharskii
Article

Abstract

The corresponding 2-(2-furyl)naphth[1,2-d]imidazoles were obtained by heating Schiff bases, prepared from 1,2-naphthalenediamine and furfural and 5-bromo- and 5-nitrofurfurals, in nitrobenzene. 2-[β-(2-Furyl)vinyl]naphth[1,2-d]imidazoles were synthesized by condensation of 2-methylnaphth[1,2-d]imidazole with furfural and 5-bromo- and 5-nitrofurfural. The methylation, nitration, and acetylation of the compounds obtained were studied, and the replacement of the bromine atom in the furan ring by a nitro group was also investigated.

Keywords

Methylation Organic Chemistry Vinyl Imidazole Schiff Base 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

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Copyright information

© Plenum Publishing Corporation 1974

Authors and Affiliations

  • L. Ya. Oleinikova
    • 1
  • F. T. Pozharskii
    • 1
  1. 1.Rostov State UniversityRostov-on-Don

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