Benzazoles. 6*. Synthesis and Arylsulfonation of 2-Hydroxymethylbenzimidazole

Abdireimov, K. B.; Mukhamedov, N. S.; Okmanov, R. Ya.; Aiymbetov, M. Zh.; Ташходжаев, Б.; Shakhidoyatov, Kh. M.

doi:10.1007/s10593-013-1307-0

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-Chloromethyl-1-(4-methylbenzene-sulfonyl) Benzimidazole (2)1

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2019

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“…At the end of the reaction, the mixture was filtered and evaporated. The obtained solid was dissolved in ethyl alcohol and column chromatography was carried out in a 1: 5 ethylacetatepetroleum ether medium to obtain a substance with 80% yield; m.p 144-145 °C [25].…”

Section: -Chloromethyl-1-(4-methylbenzene-sulfonyl) Benzimidazole (2)mentioning

confidence: 99%

Synthesis and Antimicrobial Study of New Benzimidazole Schiff Bases Bearing P-Toluene Sulfonamide Moiety

Tunç

2019

J. Chil. Chem. Soc.

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Three new Schiff bases bearing benzimidazole and p-toluen sulfonamide moiety were synthesized. Their structures were characterized by elemental analysis, FTIR, NMR and LCMS methods. The antimicrobial properties of the compounds were also evaluated. All compounds exhibit higher antimicrobial activity against all bacteria, Schiff bases (4a-4c) shows more activity than the parent aldehyde (3). 4c displays higher antibacterial activity against P. aeruginosa compare to reference drug Sulfioxazole. The compounds were found more potent against Gram-negative than Gram positive bacteria. One more free phenyl group increase the activity in 4c, but one more phenyl ring in 4b does not.In vitro antifungal activity of the compounds was also tested on fungi C. albicans C. tropicalis and C. krusei. However, our compounds exhibit no antifungal activity against three fungi.

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Section: -Chloromethyl-1-(4-methylbenzene-sulfonyl) Benzimidazole (2)mentioning

confidence: 99%