Synthesis and Acidic Properties of Some New Potential Biologically active 4 Acylamino 4 5 dihydro 1H 1 2 4 triazol 5 one Derivatives
Yazarlar (6)
Prof. Dr. Haydar YÜKSEK Kafkas Üniversitesi, Türkiye
Prof. Dr. Muzaffer ALKAN Kafkas Üniversitesi, Türkiye
Doç. Dr. Zafer OCAK Kafkas Üniversitesi, Türkiye
Prof. Dr. Şule Bahçeci Trabzon Üniversitesi, Türkiye
Prof. Dr. Miraç Ocak Karadeniz Teknik Üniversitesi, Türkiye
Mustafa Özdemir
Makale Türü Özgün Makale (SSCI, AHCI, SCI, SCI-Exp dergilerinde yayınlanan tam makale)
Dergi Adı Indian J. of Chem
Dergi ISSN 0019-5103
Dergi Tarandığı Indeksler SCI-Expanded
Makale Dili İngilizce Basım Tarihi 07-2004
Cilt / Sayı / Sayfa – / 43 / 1527–1531 DOI –
UAK Araştırma Alanları
Fen Bilgisi Eğitimi
Özet
3-Alkyl(aryl)-4-amino-4,5-dihydro-1H-1,2,4-triazol-5-ones 2 react with acyl halides such as chloroacetyl chloride, dichloroacetyl chloride and isobutyryl chloride to give the corresponding 3-alkyl(aryl)-4-chloroacetylamino-4,5-dihydro-1H-1,2,4-triazol-5-ones 3, 3-alkyl(aryl)-4-(dichloroacetylamino)-4,5-dihydro-1H-1,2,4-triazol-5-ones 4 and 3-alkyl(aryl)-4-isobutyrylamino-4,5-dihydro-1H-1,2,4-triazol-5-ones 5, respectively. The newly synthesized compounds have been characterized by elemental analyses, IR, H-1 NMR, C-13 NMR and UV spectral data. In addition, all ten new compounds are titrated potentiometrically with tetrabutylammonium hydroxide in four different non-aqueous solvents such as isopropyl alcohol, tert-butyl alcohol, acetonitrile and N,N-dimethylformamide. The half neutralization potential values and the corresponding pK(a) values have been determined for all the cases. Thus, the effects of solvents …
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BM Sürdürülebilir Kalkınma Amaçları
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