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العنوان
syntheals and study antltumor activty of some novel fused heterocyclic moietles containing nitrogen and / or sulfur heteroatoms /
المؤلف
Omer, asmaa mohamed mostfa
هيئة الاعداد
باحث / أسماء محمود مصطفي عمر
مشرف / عادل عبد الهادي نصار
مناقش / أشرف فاروق وصفي
مناقش / أميمة فرحات عثمان
الموضوع
chemistry renal cell carcinoma
تاريخ النشر
2020
عدد الصفحات
121 p :
اللغة
الإنجليزية
الدرجة
ماجستير
التخصص
Organic Chemistry
تاريخ الإجازة
10/3/2021
مكان الإجازة
جامعة المنوفية - كلية العلوم - الكيمياء
الفهرس
Only 14 pages are availabe for public view

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from 259

Abstract

This thesis is subdivided into the following chapters:
1. Introduction:
This part incudes literature survey on the chemistry, various synthetic
routes for heterocycle containing molecules is extensively studied for
their synthesis and their applications not only in medicinal chemistry, but
also in optics, electronics and material sciences.
2. Theoretical discussion:
This chapter includes the theoretical concepts of the methods adopted for
the synthesis of the designed compounds with reference to the knowledge
available in literature and structural elucidation by various spectroscopic
means.The sequences of reactions followed in the preparation of the
target compounds are summarized in the following schemes.
Synthesis of Schiff base (3) as key intermediate [1]was prepared in
excellent yield condensing by equimolar amounts of 2-cyanoaceto
hydrazide with o-bromobenzaldehyde in 50 ml absolute ethanol with 2-3
drops of glacial acetic acid as catalyst (Scheme 1).The starting compound
1,6-Diamino-4-(2-bromophenyl)-2-oxo-1,2-dihydropyridine-3,5-
dicarbonitrile (5) was prepared by two pathways (Scheme 1). The first
pathway consists of refluxing an alcoholic solution of 2-(2-
bromobenzylidene) malononitrile (2) with 2-cyanoacetohydrazide or N’-
(2-bromobenzylidene)-2-cyanoacetohydrazide (3) with malononitrile in
presence of piperidine as catalyst (Scheme1). 4-(2-bromophenyl)-2-oxo-
1,2,3,4-tetrahydropyridine-3,5-dicarbonitrile (4) was isolated (Scheme 1)
from dehydration of product (5) in presence of trifluoro acetic acid as
solvent.