2013
DOI: 10.1007/s10593-013-1383-1
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Polyfunctional Pyrazoles. 8*. Synthesis of 6-Alkyl-2-Aryl-2H-Pyrazolo[4,3-d]Pyrimidine-5,7(4H,6H)-Diones based on Ethyl 1-Aryl-4-Isocyanatopyrazole-3-Carboxylates

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Cited by 6 publications
(1 citation statement)
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“…It should be noted that the absence of signals in the downfield region (160-190 ppm) of the 13 C NMR spectra excludes the possibility for the formation of the alternative Claisen condensation/cycloaddition tandem reaction products, 9-oxo-5,7,9,10-tetrahydropyrazolo[3,4-e]tetrazolo[1,5-a]azepine-10-carboxamides. Employing the APT method for the analysis of 13 C NMR spectra and comparison with published data [8,13] allowed for a comparatively accurate assignment of signals to the corresponding carbon atoms in the triazolodiazepine cycle: C-3 (127-128 ppm), C-3a (137-139), C-5 (157-159), C-5a (141-143), C-8a (116-118), C-9 (42-43 ppm).…”
mentioning
confidence: 99%
“…It should be noted that the absence of signals in the downfield region (160-190 ppm) of the 13 C NMR spectra excludes the possibility for the formation of the alternative Claisen condensation/cycloaddition tandem reaction products, 9-oxo-5,7,9,10-tetrahydropyrazolo[3,4-e]tetrazolo[1,5-a]azepine-10-carboxamides. Employing the APT method for the analysis of 13 C NMR spectra and comparison with published data [8,13] allowed for a comparatively accurate assignment of signals to the corresponding carbon atoms in the triazolodiazepine cycle: C-3 (127-128 ppm), C-3a (137-139), C-5 (157-159), C-5a (141-143), C-8a (116-118), C-9 (42-43 ppm).…”
mentioning
confidence: 99%