000 02450cam a2200337 a 4500
003 EG-GiCUC
005 20250223032348.0
008 190828s2019 ua f m 000 0 eng d
040 _aEG-GiCUC
_beng
_cEG-GiCUC
041 0 _aeng
049 _aDeposite
097 _aM.Sc
099 _aCai01.12.10.M.Sc.2019.Ah.S
100 0 _aAhmed Sabri Abdelmoety Gabr
245 1 0 _aSynthesis of some New pyrazolo[1,5-a]pyrimidine derivatives with expected biological activity /
_cAhmed Sabri Abdelmoety Gabr ; Supervised Hussein Fouad Zohdi , Nadia Hanafy Metwally
246 1 5 _a1,5-aتشييد بعض مشتقات البيرازولو يريميدين الجديدة و المتوقع لها نشاط بيولوجى
260 _aCairo :
_bAhmed Sabri Abdelmoety Gabr ,
_c2019
300 _a100 P. ;
_c25cm
502 _aThesis (M.Sc.) - Cairo University - Faculty of Science - Department of Organic Chemistry
520 _aThe condensation of 2-(cyanomethyl)-7-(thiophen-2-yl)-5-(trifluoromethyl)pyrazolo- [1,5-a]pyrimidine-3-carbonitrile (3) with various aromatic aldehydes afforded crossponding substituted pyrazolo[1,5-a]pyrimidines 5a-j. The reaction of compound 3 with aryl diazonium chlorides in N,N-dimethylformamide furnished arylhydrazo compounds based pyrazolo[1,5-a]pyrimidine derivative. Also, reaction of compound 3 with 4-aryl azosalicylaldehydes afforded polyheterocyclic compounds based pyrazolo[1,5-a]pyrimidine derivative. The treatment of compound 3 with phenyl isothiocyanate, followed by addition of -haloesters or haloketones afforded polyheterocyclic compounds. Moreover, the enamines compound 3 react with each of hydrazine hydrate, guanidine hydrochloride to give the pyrazolo and pyrimidine derivatives. The structures of all the newly synthesized products were established by their elemental analyses, spectral data and possible mechanism has been postulated to account for their formation. The antiviral activity of some selected newly synthesized compounds was investigated
530 _aIssued also as CD
653 4 _a2-(cyanomethyl)-7-(thiophen-2-yl)-5-(trifluoromethyl)pyrazolo- [1,5-a]
653 4 _aPolyfused heterocyclic compounds
653 4 _apyrimidine-3-carbonitrile
700 0 _aHussein Fouad Zohdi ,
_eSupervisor
700 0 _aNadia Hanafy Metwally ,
_eSupervisor
856 _uhttp://172.23.153.220/th.pdf
905 _aNazla
_eRevisor
905 _aSamia
_eCataloger
942 _2ddc
_cTH
999 _c73532
_d73532