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العنوان
Peptide Synthesis of Triazolopyridine Derivatives with Expected Biological Activity /
المؤلف
Eldemerdash, Mostafa Badr Eldin Mohamed Ramadan.
هيئة الاعداد
باحث / مصطفى بدر الدين محمد رمضان الدمرداش
مناقش / محمد طه عبد العال
مشرف / محمد عبد الله حواطة
مناقش / محمد جمعة محمد عاصي
الموضوع
Organotransition metal compounds. Ligands. Lehrbuch.
تاريخ النشر
2019.
عدد الصفحات
184 p. :
اللغة
الإنجليزية
الدرجة
ماجستير
التخصص
الكيمياء
الناشر
تاريخ الإجازة
15/5/2019
مكان الإجازة
جامعة المنوفية - كلية العلوم - الكيمياء
الفهرس
Only 14 pages are availabe for public view

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from 184

Abstract

While, ethyl-6-cyano-1-(2-(2-(2-(2-(2-(2-(1-ethoxy-1-oxopropan-2-yl)hydrazinyl)-2-oxoethyl)-2H-tetrazol-5-yl)ethyl)-2H-tetrazol-5-yl)ethyl)-5-oxo-2-[(1S,2R,3S,4R)-1,2,3,4,5-pentahydroxypentyl]-7-phenyl-1,5-dihydro-[1,2,4]triazolo[1,5-a]pyridine-8-carboxylate (21) was prepared by treating of the acid hydrazide 17 with AcOH and 1N HCl and cooling at -5 oC. Sodium nitrite (NaNO2) was added and the formed ethyl-1-(2-(2-(2-(2-(2-azido-2-oxoethyl)-2H-tetrazol-5-yl)ethyl)-2H-tetrazol-5-yl)ethyl)-6-cyano-5-oxo-2-[(1S,2R,3S,4R) -1,2,3,4,5-pentahydroxypentyl]-7-phenyl-1,5-dihydro-[1,2,4]triazolo[1,5-a] pyridine-8-carboxylate (20) was treated with alanine ethyl ester in ethyl acetate containing Et3N at 0oC. The formed product was purified by recrystallization from ethanol to afford the corresponding peptide 21 in 94% yield (Scheme 19).