Araştırma Makalesi
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Yıl 2018, Sayı: 2, 39 - 48, 19.08.2018

Öz

Kaynakça

  • I.L. Finar, (1964), “Organic Chemistry, Stereochemistry and the Chemistry of Natural Products”, 3rd Edn. Longermans Green and Co Ltd., Vol.2, p. 430. M.R. Atkinson and J.B. Polya, (1954), J. Chem. Soc. Part I, 141. A.R. Katritzky and C.W. Rees, (1984), “Comprehensive heteterocyclic Chemistry; Synthesis and Uses of Heterocyclic Compounds”, Pergamon Press Ltd., England, Vol. 5, p. 744. T.B. Johnson and L.H. Chernoff, (1912), J. Am. Chem. Soc., 34, 167; Chem. Abstr.,(1912),Vol. 6, p.1156. R.G. Ghild, (1965), Organic Chemical Research Section, Lederle Laboratories, 2, 98. K.M. Daoud and H.A. Aziz, (2003), Raf. J. Sci., 15, 2, 52-57. J.B. Hendrickson, D.J. Cram and S.G. Hamond, (1970), “Organic Chemistry”, 3rd Edn. McGrow-Hill Inc., Japan, p. 967. I.L. Finar, (1975), “Organic Chemistry, Stereo Chemistry and the Chemistry of Natural Products”, 5th Ed., Longman Press Ltd., Vol. 2, pp. 433. M.Y. Shandala, M.T. Ayob and M.S Noori, (1998), Raf. J. Soc., 9, 2, 39. Guo-Xiang sun , Ming-Yan Yang , Yan-Xia Shi , Zhao-Hui Sun , Xing-Hai Liu , Hong-Ke Wu , Bao-Ju Li and Yong-Gang Zhang , (2014) , Int. J. Mol. Sci. , 15 , 8075-8090 . Rami Y. Morjan , Basam S. Qeshta , Hussein T. Al-shayyah , John M. Gardiner , Basam A. Abo-Thaher , Adel M. Awadallah , (2014) , International Journal of Organic Chemistry , 4 , 201-207 . Hakan Bakas , Nesrin Karaali , Deniz Sahin , Ahmet Demirbas , Sengul Alpay Karaoglu and Neslihan Demirbas , (2010) , Molecules , 15 , 2427-2438 . Stefania-Felicia Barbuceanu , Diana Carolina Ilies , Gabriel Saramet , Valentina Uivarosi , Constantin Draghici and Valeria Raulescu , (2014) , Int. J. Mol. Sci. , 15 , 10908-10925 . Mariam Al-sheikh , Hanadi Y. Medrasi , Kamal Usef Sadek and Ramadan Ahmed Mekheimer , (2014) , Molecules , 19 , 2993-3003. Mahmoud R. Mahmoud , Wael S.I. Abou-Elmagd , Manal M. El-Shahawi and Mohamed H. Hekal , (2014) , World Journal of Chemistry , 9 , (2) , 24-32 . E.R. Bochman, C.M. Mc-Closkey and J.A. Seneker, (1947), J. Am. Chem. Soc., 69, 380. H.L. Yale, K. Losee, J. Martins, M. Holsing, F.M. Perry and J. Bernstein, (1953) , J. Am. Chem. Soc., 75, 1933. B.S. Holla, M.K. Shivanada, P.M. Akberali, S. Balige and S. Safeer, (1996), Farmaco., 51(12), 785. U. Misra, A. Hitkari, A. Saxena, S. Gurtu and K. Shanker, (1996), Eur. J. Med. Chem., 31, 629-634. A.K. Sen-Gupta and K. Hajela, (1981), J. Indian Chem. Soc., LVIII, 690. K.T. Potts and R.M. Huseby, (1966), J. Org. Chem., 31, 9, 3528. Liu , X.H. ; Chen , P.Q. ; Wang , B.L. ; Wang S.H.; Li, Z.M., (2007), Bioorg. Med. Chem. Lett., 17 , 3784-3788.

New Fused Hyterocyclic Compounds: Synthesis of Some 1,4-di[1,2,4- Triazoles[3,4-b]5-phnyl/aryl-1,3,4-thiadiazole] Benzene

Yıl 2018, Sayı: 2, 39 - 48, 19.08.2018

Öz

In
this paper the synthesis of some substituted di – 1,2,4-triazoles and it is
conversion to multi nuclear heterocyclic compounds ; described Terphthalic acid
was esterified to its ethyl ester(1)by its reaction with absolute ethanol ,
concentrated sulfuric acid , the ethyl ester (1) was treated with hydrazine
hydrate is ethanol to give the acid hydrazide (2). the hydrazide (2) then
treated with ammonium thiocyanate to give thiosemicarbazide (3) , reaction of
thiosemicarbazide (3) with  hydrazine
hydrate gave  1,4-bis(
3-thiol-4-amino-1,2,4-triazole-5-yl) benzene (4). Compound (4) treatment with
three type substituted benzaldehyde gave 1,4-di hydrazones phenyl (5,6 and 7).
Cyclization hydrazones compounds (5,6,7) with phosphorous oxychloride in xylene
to gave bicyclic system 1,4-bis[1,2,4-triazole[3,4-b]-5-substituted –
1,3,4-thiadiazole] benzene (8,9 and 10) 
. On the other hand some physical parameters of compounds ( 4 -10 )
under investigation such as the Mullikan charge at the active atoms, HOMO and
LUMO energy levels , hardness (η) , electronic chemical potential (µ) and global electrophilicty index (W) were theoretically calculated using ( Gaussian program ). The
antibacterial activity some of the synthesis compounds was studied. The
structures of the synthesized compounds were confirmed by physical and spectral
methods.

Kaynakça

  • I.L. Finar, (1964), “Organic Chemistry, Stereochemistry and the Chemistry of Natural Products”, 3rd Edn. Longermans Green and Co Ltd., Vol.2, p. 430. M.R. Atkinson and J.B. Polya, (1954), J. Chem. Soc. Part I, 141. A.R. Katritzky and C.W. Rees, (1984), “Comprehensive heteterocyclic Chemistry; Synthesis and Uses of Heterocyclic Compounds”, Pergamon Press Ltd., England, Vol. 5, p. 744. T.B. Johnson and L.H. Chernoff, (1912), J. Am. Chem. Soc., 34, 167; Chem. Abstr.,(1912),Vol. 6, p.1156. R.G. Ghild, (1965), Organic Chemical Research Section, Lederle Laboratories, 2, 98. K.M. Daoud and H.A. Aziz, (2003), Raf. J. Sci., 15, 2, 52-57. J.B. Hendrickson, D.J. Cram and S.G. Hamond, (1970), “Organic Chemistry”, 3rd Edn. McGrow-Hill Inc., Japan, p. 967. I.L. Finar, (1975), “Organic Chemistry, Stereo Chemistry and the Chemistry of Natural Products”, 5th Ed., Longman Press Ltd., Vol. 2, pp. 433. M.Y. Shandala, M.T. Ayob and M.S Noori, (1998), Raf. J. Soc., 9, 2, 39. Guo-Xiang sun , Ming-Yan Yang , Yan-Xia Shi , Zhao-Hui Sun , Xing-Hai Liu , Hong-Ke Wu , Bao-Ju Li and Yong-Gang Zhang , (2014) , Int. J. Mol. Sci. , 15 , 8075-8090 . Rami Y. Morjan , Basam S. Qeshta , Hussein T. Al-shayyah , John M. Gardiner , Basam A. Abo-Thaher , Adel M. Awadallah , (2014) , International Journal of Organic Chemistry , 4 , 201-207 . Hakan Bakas , Nesrin Karaali , Deniz Sahin , Ahmet Demirbas , Sengul Alpay Karaoglu and Neslihan Demirbas , (2010) , Molecules , 15 , 2427-2438 . Stefania-Felicia Barbuceanu , Diana Carolina Ilies , Gabriel Saramet , Valentina Uivarosi , Constantin Draghici and Valeria Raulescu , (2014) , Int. J. Mol. Sci. , 15 , 10908-10925 . Mariam Al-sheikh , Hanadi Y. Medrasi , Kamal Usef Sadek and Ramadan Ahmed Mekheimer , (2014) , Molecules , 19 , 2993-3003. Mahmoud R. Mahmoud , Wael S.I. Abou-Elmagd , Manal M. El-Shahawi and Mohamed H. Hekal , (2014) , World Journal of Chemistry , 9 , (2) , 24-32 . E.R. Bochman, C.M. Mc-Closkey and J.A. Seneker, (1947), J. Am. Chem. Soc., 69, 380. H.L. Yale, K. Losee, J. Martins, M. Holsing, F.M. Perry and J. Bernstein, (1953) , J. Am. Chem. Soc., 75, 1933. B.S. Holla, M.K. Shivanada, P.M. Akberali, S. Balige and S. Safeer, (1996), Farmaco., 51(12), 785. U. Misra, A. Hitkari, A. Saxena, S. Gurtu and K. Shanker, (1996), Eur. J. Med. Chem., 31, 629-634. A.K. Sen-Gupta and K. Hajela, (1981), J. Indian Chem. Soc., LVIII, 690. K.T. Potts and R.M. Huseby, (1966), J. Org. Chem., 31, 9, 3528. Liu , X.H. ; Chen , P.Q. ; Wang , B.L. ; Wang S.H.; Li, Z.M., (2007), Bioorg. Med. Chem. Lett., 17 , 3784-3788.
Toplam 1 adet kaynakça vardır.

Ayrıntılar

Birincil Dil İngilizce
Konular Mühendislik
Bölüm Makaleler
Yazarlar

Mohanad Yakdhan Saleh

Yayımlanma Tarihi 19 Ağustos 2018
Yayımlandığı Sayı Yıl 2018Sayı: 2

Kaynak Göster

APA Saleh, M. Y. (2018). New Fused Hyterocyclic Compounds: Synthesis of Some 1,4-di[1,2,4- Triazoles[3,4-b]5-phnyl/aryl-1,3,4-thiadiazole] Benzene. The Eurasia Proceedings of Science Technology Engineering and Mathematics(2), 39-48.