Synthesis and Biological Activities of Some New Derivatives Based on ۵-Styryl-۲-amino-۱,۳,۴-thiadiazole
Publish place: Chemical Methodologies، Vol: 6، Issue: 2
Publish Year: 1401
نوع سند: مقاله ژورنالی
زبان: English
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شناسه ملی سند علمی:
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.
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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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