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JOURNALS // Mendeleev Communications // Archive

Mendeleev Commun., 2001 Volume 11, Issue 5, Pages 201–203 (Mi mendc4293)

This article is cited in 8 papers

Iodocyclization of N-(2-nitrophenyl)- and N-phenyl-N’-[2-(alk-1-enyl)phenyl]ethanimidamides

I. S. Afon'kin, A. A. Fatykhov, L. V. Spirikhin, I. B. Abdrakhmanov

Ufa Institute of Chemistry, Ufa Federal Research Centre of the Russian Academy of Sciences, Ufa, Russian Federation

Abstract: The action of iodine on N-(2-nitrophenyl)- or N-phenyl-N’-[2-(alk-1-enyl)phenyl]ethanimidamides obtained by the condensation of 2-(cyclopent-1-enyl)-6-methylaniline with N-(1-chloroethylidene)aniline or N-(1-chloroethylidene)-2-nitroaniline results in corresponding spiro(3,4-dihydroquinazoline)-4,1’-(2’-iodocyclopentane) in good yields, but the analoguous reaction with 4-methyl-2- (1-methylbut-1-enyl)aniline leads to an N-[(2,3-dihydro-1H-indol-1-yl)ethyl]ideneaniline derivative.

Language: English

DOI: 10.1070/MC2001v011n05ABEH001490



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