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首页> 外文期刊>Revue roumaine de chimie >REACTIONS OF 3-AMINO-5-METHYLISOXAZOLE WITH ENOL ETHERS: SYNTHESIS OF NEW ISOXAZOLYLENAMINES DERIVATIVES AND SUBSTITUTED ISOXAZOLO[2,3-a]PYRIMIDINONES
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REACTIONS OF 3-AMINO-5-METHYLISOXAZOLE WITH ENOL ETHERS: SYNTHESIS OF NEW ISOXAZOLYLENAMINES DERIVATIVES AND SUBSTITUTED ISOXAZOLO[2,3-a]PYRIMIDINONES

机译:3-氨基-5-甲基异恶唑与烯醇醚的反应:合成新的异恶唑啉酮衍生物和取代的异恶唑啉[2,3-a]嘧啶酮

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摘要

A new series of isoxazolylenamines and substituted isoxazolo[2,3-a]pyrimidinones were prepared via condensation of ethoxymethylenemalonate 2a-d and ethoxymethylenecyanoacetate 2e-h with 3-amino-5-methylisoxazole 1. When reactions were carried out under reflux in xylene, the thermal cyclisation of isoxazolylenamines intermediates 3a-d afforded exclusively the isoxazolo-[2,3-a]pyrimidinones 4a-d. All the synthesized compounds were characterized by elemental analysis, MS, IR and NMR spectrometry.
机译:通过乙氧基丙二酸丙二酸酯2a-d和乙氧基氰基乙二酸酯2e-h与3-氨基-5-甲基异恶唑1缩合制备一系列新的异恶唑基亚胺基和取代的异恶唑并[2,3-a]嘧啶酮。异恶唑啉亚胺中间体3a-d的热环化仅提供了异恶唑-[2,3-a]嘧啶酮4a-d。所有合成的化合物均通过元素分析,MS,IR和NMR光谱进行表征。

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