<span style="font-size:20.5pt;mso-bidi-font-size:14.5pt; font-family:"Times New Roman";mso-fareast-font-family:"Times New Roman"; mso-ansi-language:EN-US;mso-fareast-language:EN-US;mso-bidi-language:AR-SA; mso-bidi-font-weight:bold">Synthesis and novel reactions of 2,3-dimethyl-1<i style="mso-bidi-font-style:normal">H</i>-pyrrolo[1,2-<i style="mso-bidi-font-style: normal">a</i>]benzimidazol- 1-one with secondary amines and <i><span style="font-size:20.5pt;mso-bidi-font-size:14.5pt;font-family:Arial;mso-fareast-font-family: "Times New Roman";mso-ansi-language:EN-US;mso-fareast-language:EN-US; mso-bidi-language:AR-SA;mso-bidi-font-weight:bold">N </span></i><span style="font-size:20.5pt;mso-bidi-font-size:14.5pt;font-family:"Times New Roman"; mso-fareast-font-family:"Times New Roman";mso-ansi-language:EN-US;mso-fareast-language: EN-US;mso-bidi-language:AR-SA;mso-bidi-font-weight:bold">-bromosuccinimide</span></span>

Abstract

312-316N, <span style="font-size:13.0pt;mso-bidi-font-size:7.0pt;font-family:HiddenHorzOCR; mso-bidi-font-family:HiddenHorzOCR">N-Disubstituted-β<span style="font-size:13.0pt;mso-bidi-font-size:7.0pt;font-family:HiddenHorzOCR; mso-bidi-font-family:HiddenHorzOCR">-(2-benzimidazolyl)-, β-dimethylacrylamides 5<b style="mso-bidi-font-weight: normal">Aa-g and 5Ba-g , 2-bromomethyl-3- methyl-1 H-pyrrolo[1,2<i style="mso-bidi-font-style: normal">a]benzimidazol-1-one 8A and 2,3-dimethyl-1H-pyrrolo[1,2a]benzimidazole-1-thione 10A have been synthesized from 2,3-dimethyl-1 H<span style="font-size:15.0pt; mso-bidi-font-size:9.0pt;font-family:" times="" new="" roman";mso-fareast-font-family:="" "times="" roman";mso-ansi-language:en-us;mso-fareast-language:en-us;="" mso-bidi-language:ar-sa;mso-bidi-font-style:italic"="">-pyrrolo [1,2a]benzimidazol-1-one <b style="mso-bidi-font-weight: normal">4A. Compounds 5Aa-g and 5Ba-g have been synthesized via two different routes. These compounds have been screened for their antimicrobial and anthelmintic activities.</span

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