Synthesis and antimicrobial activity of 2-aryloxy-2,3-dihydro-5-propylthio-1<i style="mso-bidi-font-style:normal">H</i>-1,3,2- <span style="font-size:12.0pt;font-family:"Times New Roman"; mso-fareast-font-family:"Times New Roman";mso-ansi-language:EN-IN;mso-fareast-language: EN-IN;mso-bidi-language:AR-SA" lang="EN-IN">benzodiazaphosphole 2-oxides</span>

Abstract

2-Aryloxy-2,3-dihydro-5-propylthio-1<i style="mso-bidi-font-style: normal">H</i>-1,3,2-benzodiaza-phosphole 2-oxides <b style="mso-bidi-font-weight: normal">3</b> are synthesized by reacting equimolar quantities of 4-propylthio-1,2-phenylenediamine <b style="mso-bidi-font-weight:normal">1</b> with different arylphosphorodichloridates in the presence of triethylamine at 60-

<span style="font-size:12.0pt;font-family:" times="" new="" roman";="" mso-fareast-font-family:"times="" roman";mso-ansi-language:en-in;mso-fareast-language:="" en-in;mso-bidi-language:ar-sa"="" lang="EN-IN">70°C. IR, ¹H, ¹³C and ³¹P NMR spectral data are discussed. All of these compounds have been screened for their antifungal and antibacterial activities.</span>