4.4 Article

Facile Synthesis of New Imidazoles from Direct Reaction of 2,3-Diamino-1,4-naphthoquinone with Aldehydes

Journal

JOURNAL OF HETEROCYCLIC CHEMISTRY
Volume 48, Issue 4, Pages 787-791

Publisher

WILEY
DOI: 10.1002/jhet.582

Keywords

-

Ask authors/readers for more resources

New imidazoles were easily prepared from 2,3-diamino-1,4-naphthoquinone and stoichiometric quantities of the appropriate aldehydes in dimethyl sulfoxide as a solvent. The reaction proceeded for few hours. The procedure can be generalized to different classes of aldehydes. 2-Methyl-1H-naphtho[2,3-d]imidazole-4,9-dione was also obtained in good yield during refluxing of 2,3-diaminonaphthoquinone in acetic acid. The structure of the newly synthesized imidazoles was extensively investigated using NMR experiments.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.4
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available