Synthesis and antimicrobial activity of new 2-azetidinones from N-(salicylidene) amines and 2-diazo-1,2-diarylethanones

Journal article

Authors / Editors

Pheko, Tshepo

Research Areas

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Publication Details

Author list: Singh GS, Mbukwa E, Pheko T

Place: GAINESVILLE

Publication year: 2007

Journal: ARKIVOC (1551-7004)

Journal acronym: ARKIVOC

Start page: 80

End page: 90

Number of pages: 11

ISSN: 1424-6376

Languages: English-Great Britain (EN-GB)

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Abstract

This paper describes the reactions of N-salicylideneamines with diarylketenes generated from thermal decomposition of the 2-diazo-1,2-diarylethanones. An equimolar reaction of the N-salicylidenebenzhydrylamine with diphenylketene affords a mixture of 2[(benzhydrylimino) methyl] phenyl- 2,2- diphenylacetate as a major product and 1-benzhydryl-3,3diphenyl-4-[2'-(O-diphenylacyl) hydroxyphenyl]-2-azetidinone as a minor product. The reactions of various N-salicylideneamines with 2.2 molar equivalents of 2-diazo-1,2-diarylethanones have been carried out to afford 1- substituted-3,3-diaryl-4-[2'-(O-diarylacyl) hydroxyphenyl]- 2-azetidinones as sole product in excellent yields. The products, characterized on the basis of satisfactory analytical and spectral data, have shown moderate to good antimicrobial activity against some bacteria and fungi. Among the fourteen compounds in the series, the 2-azetidinone 4l with a 4-chlorophenyl group on beta- lactam ring nitrogen and 4-methylphenyl groups on beta-lactam ring C- 3 position is the most active compound.

Keywords

2-azetidinones, antimicrobial, cycloaddition, diarylketenes, iminophenols

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