Synthesis and Biological Activities of Some New Derivatives Based on ۵-Styryl-۲-amino-۱,۳,۴-thiadiazole

Publish Year: 1401
نوع سند: مقاله ژورنالی
زبان: English
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JR_CHM-6-2_001

تاریخ نمایه سازی: 11 دی 1400

Abstract:

In this research, ۵-Styryli-۲-amino-۱, ۳, ۴-thiadiazole [C۱] was prepared from the reaction of acid ۳-phenyl propenoic acid with thiosemicarbazide. Amic acids [C۲-C۵] were synthesized by reactive compound [C۱] with different types of hydrides, then [C۲, C۴] were treated with AC۲O in the presence of NaOAC as a catalyst giving Imide compounds [C۶, C۷]. The structure of the new derivatives was confirmed via FT-IR spectroscopy, some of which were confirmed via ۱H-NMR spectroscopy. Three of these new derivatives were evaluated by their Esherichiacoli, Staphylococcus, and Rhizopus emporium.

Authors

Shetha Fadhil Narran

Department of Chemistry, College of Science for women, University of Baghdad, Baghdad, Iraq

Suad Salman Mohammed

Department of Chemistry, College of Science for women, University of Baghdad, Baghdad, Iraq

Maab Khattab Omer

Department of Chemistry, College of Science for women, University of Baghdad, Baghdad, Iraq

Iftikhar Ahmed Hussein

Department of Chemistry, College of Science for women, University of Baghdad, Baghdad, Iraq

Noor Mohammed Jawad

Department of Chemistry, College of Science for women, University of Baghdad, Baghdad, Iraq

Batool Karim Shweish

Department of Chemistry, College of Science for women, University of Baghdad, Baghdad, Iraq

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