Abstract
A hexachlorocyclotriphosphazene (HCCP)-mediated direct formation of quinazoline (thio)ethers from quinazolin-4(3H)-ones has been developed. Treatment of quinazolin-4(3H)-ones with HCCP, diisopropylethylamine (DIPEA), and thiophenols resulted in formation of the corresponding 4-arylthioquinazoline derivatives in moderate to excellent yields. This method has also been utilized to prepare 4-aryloxyquinazoline and 4-alkoxyquinazoline derivatives using phenols and sodium alkoxides as the nucleophiles. © 1996-2013 MDPI AG (Basel, Switzerland).
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Hu, B., Zhang, X., Sheng, L., Guo, M., Shen, Z., Hu, X., … Mo, W. (2013). Hexachlorocyclotriphosphazene (HCCP)-mediated direct formation of thioethers and ethers from quinazolin-4(3H)-ones. Molecules, 18(5), 5580–5593. https://doi.org/10.3390/molecules18055580
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