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العنوان
SYNTHESIS OF DIPICOLINIC ACID DERIVATIVES OF EXPECTED BIOLOGICAL ACTIVITY \
المؤلف
AMR,ABD EL-GALIL B.A.
هيئة الاعداد
مشرف / عبد الجواد محمد ربيع
مشرف / عبد الحميد محمود عطية
باحث / عبد الجليل السيد عبد الرحمن
مناقش / عبد الجواد محمد ربيع
تاريخ النشر
1998.
عدد الصفحات
238p.;
اللغة
الإنجليزية
الدرجة
الدكتوراه
التخصص
الكيمياء
تاريخ الإجازة
1/1/1998
مكان الإجازة
جامعة عين شمس - كلية العلوم - الكيماء
الفهرس
Only 14 pages are availabe for public view

from 32

from 32

Abstract

1. The thesis startes with an introduction covering a general review for the chemistry of
2,6-pyridinedicarboxylic acid (dipicolinic acid) till 1997. It includes also a special part
presenting the obtained results followed by the experimental part and ended with a list of 280
references.
2. The thesis includes a course of investigation to synthesize a series of some peptide
derivatives. Coupling of 2,6-pyridine dipicolinoyl dichloride (23) with amino acid methyl esters to
afford 2,6-bis­ (aminocarbonyl)pyridine methyl ester derivatives (125) was preformed followed by
treating with hydrazine hydrate to give the corresponding dihydrazide derivatives (126).
. o (’nNI o
NH
O







0 _R
a a







b_H _CO_O_M_e







., R’t’NH ’NH!R
Ao o o







NAy TEA
(23)







o
I I
CH3 CH3
(125)











(126)
3. Some dihydrazone derivatives (127) have been prepared from the reaction of the diydrazide
derivatives (126) with benzaldehyde or p-chlorobenzaldehyde.




(127)
4- Hydrolysis of diesters (125) with sodium hydroxide gave the corresponding diacid derivatives
(128).

0


(128)
5- Dihydrazide derivatives (88) and (126) reacted with some acid · anhydrides to give
the corresponding diamide-(129) and tetraamidediimide derivatives (130), respectively.



(129) (130)
6. Condensation of dihydrazides (88) and (126) with some tetra­ carboxylic acid dianhydrides,
namely I ,2,4,5-benzenetetra­ carboxylic acid dianhydride or I ,4,5,8-naphthalenetetracarboxylic
acid dianhydride was undertaken to afford different macrocyclic polyamide derivatives (131) and
(132), respectively.









0y-”N-”y0









0y-”N-”y0









:a:a :











oNu_;o(











oNu_;o(












(131a) (131b)