Preparation and NMR spectra of substituted 2-phenyl-5,5-dialkylimidazolinones
✍ Scribed by Miloš Sedlák; Aleš Halama; Petr Mitaš; Jaromír Kaválek; Vladimír Macháček
- Publisher
- Journal of Heterocyclic Chemistry
- Year
- 1997
- Tongue
- English
- Weight
- 334 KB
- Volume
- 34
- Category
- Article
- ISSN
- 0022-152X
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✦ Synopsis
Abstract
Eighteen substituted 2‐phenyl‐5,5‐dialkylimidazolinones 2 have been prepared by cyclizations of substituted 2‐(N‐benzoylamino)alkanamides 1. The cyclization of methylamides 1 proceeds at room temperature whereas primary amides are cyclized on boiling. The ^1^H and ^13^C nmr spectra of the imidazolinones are presented and the changes in their spectra connected with their protonation in hexadeuteriodimethyl sulfoxide‐trifluoroacetic acid mixtures are discussed.
📜 SIMILAR VOLUMES
NMR-Spectra of 1-[2,4,5-triphenyl-2-cyclopentenyl]phenyl ketone and 1-[2,4,5-triphenyI-1 -cyclopentenyl]phenyl ketone indicate that the coupling constants of vicinal hydrogens in the cyclopentene ring vary with structure.
## Abstract New high yield preparation methods were developed for the pharmaceutically interesting compounds, 1‐benzyl‐, 1‐methyl‐, and 1__H__‐5‐[(2‐oxo‐2‐phenyl)ethyl]imidazoles **1a‐c**, respectively. The title compounds were synthesized by four different methods using various starting materials.
## Abstract Carbon‐13 NMR chemical shifts and carbon‐proton coupling constants for nine 4‐substituted and six 5‐substituted pyrimidines are reported. The carbon chemical shifts are correlated with π‐electron densities. Carbon‐proton coupling constants fail to correlate with substituent electronegat
## Abstract ^1^H and ^13^C NMR spectra of 22 2‐substituted 4,5‐dimethylfurans are reported. The __J__(C, H) values were used for signal assignments and for the identification of geometrical isomers of some derivatives.