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首页> 外文期刊>European journal of organic chemistry >Transition-metal-catalyzed hydroamination and carboamination reactions of anthranilic allenamides as a route to 2-Vinyl- and 2-(α-Styryl)quinazolin- 4-one derivatives
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Transition-metal-catalyzed hydroamination and carboamination reactions of anthranilic allenamides as a route to 2-Vinyl- and 2-(α-Styryl)quinazolin- 4-one derivatives

机译:过渡金属催化的邻氨基苯甲酰胺类化合物的加氢氨化和碳氨化反应,作为2-乙烯基和2-(α-苯乙烯基)喹唑啉-4-酮衍生物的途径

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摘要

2-Vinyl- and 2-(α-styryl)quinazolin-4-ones have been synthesized by intramolecular gold-catalyzed hydroamination and palladium-catalyzed carboamination of anthranilic allenamides, easily prepared by prototropic isomerization of the corresponding propargylamides. These procedures, which lead to N-Boc-protected quinazolinones, represent a more flexible alternative to the reported palladium-catalyzedamination of anthranilic allylamides, achievable only from N-tosylallylamides.
机译:2-乙烯基和2-(α-苯乙烯基)喹唑啉-4-酮是通过分子内金催化的邻氨基苯甲酰胺的加氢氨化和钯催化的碳氨化反应合成的,可以通过相应的炔丙基酰胺的质子异构化容易地制备。这些导致N-Boc保护的喹唑啉酮的方法代表了报道的邻氨基苯甲酰胺的钯催化催化氨基化的更灵活的替代方法,后者只能从N-甲苯磺酰芳酰胺中获得。

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