Dergiler / Hacettepe Journal of Biology and Chemistry / 2019 / Cilt: 47 - Sayı: 2

Investigation of Reaction of Some Ester Ethoxycarbonyl Hydrazones with 1-Adamantyl Amine

Sayfa
203–208
Yayın Tarihi
2019-09-18
DOI
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⚡ TL;DR(1 Cümlede Hızlı Çıkarım)

The structures of the synthesized compounds were elucidated by spectroscopic methods using IR, ¹H-NMR, 13C-NMR spectra and LC/MS analysis.

📌 3 Maddede Bu Makale

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Amaç & Hipotez:I n this study, the reactions of the 1-adamantyl amine with 4 different ester ethoxycarbonyl hydrazone derivatives were studied.
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Temel Bulgular & Veri:In the last step, 3-substituted-4-adamantyl-1,2,4-triazol-5-one derivatives were aimed to synthesize, the ester ethoxycarbonyl hydrazone compounds were heated in an oil bath dry to dry with 1-adamantyl amine.
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Sonuç & Katkı:The structures of the synthesized compounds were elucidated by spectroscopic methods using IR, ¹H-NMR, 13C-NMR spectra and LC/MS analysis.
🔬Tür:Araştırma Makalesi
📍Kapsam:Genişletilmiş Akademik Örneklem
⚙️Değişkenler:1-adamantyl amine · ester ethoxycarbonyl hydrazone · iminoester hydrochlorides

Abstract

I n this study, the reactions of the 1-adamantyl amine with 4 different ester ethoxycarbonyl hydrazone derivatives were studied. At first, iminoester hydrochloride derivatives were synthesized according to the Pinner method. Then they were reacted with ethyl carbazate to synthesize ester ethoxycarbonyl hydrazone derivative compounds. In the last step, 3-substituted-4-adamantyl-1,2,4-triazol-5-one derivatives were aimed to synthesize, the ester ethoxycarbonyl hydrazone compounds were heated in an oil bath dry to dry with 1-adamantyl amine. It has been observed, however, that the ring is not closed according to IR and ¹H-NMR analysis and the ethyl N-(adamantylcarbamoyl)alkylcarbohydrazonoate derivative compounds were synthesized as stabile and original compounds. The structures of the synthesized compounds were elucidated by spectroscopic methods using IR, ¹H-NMR, 13C-NMR spectra and LC/MS analysis.

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Bu Makaleye Atıf Yap

DOĞAN, İ. S., SELLİTEPE, H. E., KAHVECİ, B. (2019). Investigation of Reaction of Some Ester Ethoxycarbonyl Hydrazones with 1-Adamantyl Amine. Hacettepe Journal of Biology and Chemistry, Cilt: 47 - Sayı: 2, 203–208. https://ajindex.com/articles/255734

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Kaynakça (12)

  1. J. Warren, Drug discovery: lessons from evolution, Br. J. Clin. Pharmacol., 71 (2011) 497-503
  2. H.U. Daeniker, 1‐Hydrazinoadamantan, Helvetica Chimica Acta., 50 (1967) 2008-2010
  3. T.L. Thomas, M. Fedorchuk, B.V. Shetty, F.E. Anderson, Synthesis and activity of some 3-substituted 1,2,3,4-pseudooxatriazol-5-ones and their precursors and related compounds, J. Med. Chem., 13 (1970) 196-203
  4. M.G. Alves Galvão, M.A. Rocha Crispino Santos, A.J. Alves da Cunha, Amantadine and rimantadine for influenza A in children and the elderly, Cochrane Database Syst Rev., 21 (2014) CD002745
  5. K. Spilovska, F. Zemek, J. Korabecny, E. Nepovimova, O. Soukup, M. Windisch, K. Kuca, Adamantane - A lead structure for drugs in clinical practice, Curr. Med. Chem., 23 (2016) 3245-3266
  6. S.V. Krapivin, S.A. Sergeeva, I.S. Morozov, Comparative analysis of the effects of adapromine, midantane, and bromantane on bioelectrical activity of rat brain, Bull. Exp. Biol. Med. 125 (1998) 175-179
  7. R. Naik, H. Valentine, A. Hall, W.B. Mathews, J.C. Harris, C.S. Carter, R.F. Dannals, D.F. Wong, A.G. Horti, Development of a radioligand for imaging V1a vasopressin receptors with PET, Eur. J. Med. Chem., 139 (2017) 644-656
  8. M. Kamenova-Nacheva, M. Schröder, E Pasheva, I. Slavchev, V. Dimitrov, G. Momekov, R. Nikolova, B. Shivachev, I. Ugrinova, G.M. Dobrikov, Synthesis of ferrocenylmethylidene and arylidene substituted camphane based compounds as potential anticancer agents, New J. Chem., 41 (2017) 9103- 9112
  9. U. Kalita, S. Kaping, R. Nongkynrih, I. Boiss, L. Indira Singha, J. Narain Vishwakarma, Design, synthesis, structure elucidation, and biological activities of 3-(substituted amino)-1-(pyridin-4-yl)propenones and 5-isonicotinoyl1,2,3,4-tetrahydropyrimidine–adamantane hybrids, Monatshefte für Chemie., 148 (2017) 2155-2171
  10. A.N. Balaev, V.N. Osipov, K.A. Okhmanovich, E.A. Ruchko, M.A. Baryshnikova, D.S. Khachatryan, Pentapeptide analogs of somatostatin containing a thiazolidine fragment: synthesis and cytotoxic activity, Russian Chemical Bulletin., 65 (2016) 2948-2951
  11. Y. Shi, Y.H. Duan, Y.Y. Ji, Z.L. Wang, Y.R. Wu, H. Gunosewoyo, X.Y. Xie, J.Z. Chen, F. Yang, J. Li, J. Tang, X. Xie, L.F. Yu, Amidoalkylindoles as potent and selective cannabinoid type 2 receptor agonists with in vivo efficacy in a mouse model of multiple sclerosis, J. Med. Chem., 60 (2017) 7067-7083
  12. A. Quéméner, M. Maillasson, L. Arzel, B. Sicard, R. Vomiandry, E. Mortier, D. Dubreuil, Y. Jacques,