A facile and efficient method has been developed for the synthesis of quinoline-fused fluorescent dihydro/spiro-quinazolinones. A plausible mechanism involving an acid-mediated enaminone intermediate is provided. The reaction proceeded using p-toluene sulfonic acid as a green promoter. The methodology was successful in synthesizing various quinoline-appended spiro-quinazolinones 4a-o. The synthetic utility of compounds 4a-o was demonstrated by synthesizing compounds 6a-d via Suzuki coupling as a key reaction. Significantly, the π-π∗ electronic transition of compounds 4c and 4k showed a blue shift. The molar extinction coefficient (ϵ), Stoke's shift (Δū), and quantum yield (φf)cwere calculated for these derivatives (4c and 4k).
CITATION STYLE
George, K., Elavarasan, P., Ponnusamy, S., & Sathananthan, K. (2022). Facile One-Pot Synthesis of Functionalized Quinoline-Fused Fluorescent Dihydro/Spiro-quinazolinone Derivatives. ACS Omega, 7(24), 20605–20618. https://doi.org/10.1021/acsomega.2c00674
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