Thiosemicarbazones Synthesized from Acetophenones: Tautomerism, Spectrometric Data, Reactivity and Theoretical Calculations

Abstract

Tautomeric forms of Thiosemicarbazones have been investigated by spectrometric methods, their chemical reactivity and theoretical calculations of the relative tautomers stabilities. The mass spectral fragmentation of thiosemicarbazones synthesized from acetophenones has been studied by CG/MS. The analysis of the corresponding spectra shows not only the regular fragmentation mechanisms but homolytic ruptures from even-electron species. 1 H NMR spectra exhibit signals for the most intense open thioketo tautomeric structure, although when using TFA a ring structure is observed in the corresponding tautomeric equilibrium. Density Functional Theory calculations (DFT) also provide evidence to support the experimental observations by GC-MS and 1 H NMR. Methylation reactions give support to the occurrence of the thioenol tautomeric form which would be the second most abundant according to the Density Functional Theoretical calculations.

Novel thiazole derivatives incorporating phenyl sulphonyl moiety as potent BRAFV600E kinase inhibitors targeting melanoma

“…46,47 It is worth mentioning that the chemical shi values observed for all the NH protons in the presence of phenylsulfonylmethylene group showed a down-eld shi of approximately +0.40 to +1.3 ppm compared to the previously reported analog lacking phenylsulfonylmethylene group. 48 Also, the 13 C NMR spectrum of the carbothioamide derivative 3 showed a signal at d ¼ 179 ppm assigned to the C]S group, in addition to another signal at d ¼ 139 ppm corresponding to C]N.…”