Abstract
The corresponding 2,3-diphenyl[3,2-a]pyrimidinium salts were obtained by the condensation of 4,5-diphenyl-2-aminothiazole perchlorate with β-diketones, β-chlorovinyl ketones, β-chlorovinyl aldehydes, and 1,1,3,3-tetraethoxypropane. The PMR spectra were used to prove the structures of the compounds obtained, particularly to select the structures of the isomeric salts obtained in the condensation with unsymmetrical β-diketones, β-chlorovinyl ketones, and β-chlorovinyl aldehydes. As a rule, the latter give one isomer — the γ-unsubstituted (relative to the bridge nitrogen atom) derivative.
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Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 5, pp. 629–631, May, 1972.
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Shul'ga, S.I., Fursaeva, N.F. & Chuiguk, V.A. 2,3-Diphenylthiazolo[3,2-a]pyrimidinium salts. Chem Heterocycl Compd 8, 568–570 (1972). https://doi.org/10.1007/BF00488146
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DOI: https://doi.org/10.1007/BF00488146