Abstract

AbstractSynthesis of some new 2‐(alkoxy carbonyl alkyl)‐6‐bromo‐3,4‐dihydro‐3‐(α‐methyl benzyl)‐2‐oxo‐3‐benzo‐ [e][2H‐1,3,2‐oxazaphosphinine] derivatives was accomplished through a two step process, which involves the condensation of 2‐[(α‐methylbenzyl amino)methyl]‐4‐bromophenol (1) with phosphorus oxychloride in equimolar quantities in the presence of triethylamine in dry toluene in 50–55 °C producing the corresponding intermediate (2), and subsequent reaction with the amino acid alkyl ester in dry tetrahydrofuran in the presence of triethylamine at different temperatures. They exhibited significant antibacterial and fungal activity.

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