首页> 外文期刊>RSC Advances >Intramolecular C-O/C-S bond insertion of alpha-diazoesters for the synthesis of 2-aryl-4H-benzo[d][1,3]oxazine and 2-aryl-4H-benzo[d][1,3]thiazine derivatives
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Intramolecular C-O/C-S bond insertion of alpha-diazoesters for the synthesis of 2-aryl-4H-benzo[d][1,3]oxazine and 2-aryl-4H-benzo[d][1,3]thiazine derivatives

机译:α-重氮酸酯的分子内C-O / C-S键插入,用于合成2-芳基-4H-苯并[d] [1,3]恶嗪和2-芳基-4H-苯并[d] [1,3]噻嗪衍生物

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摘要

An intramolecular C-O insertion of 2-(2-arylamidophenyl)-2-diazoacetate has been achieved using a catalytic amount of copper triflate under mild conditions to produce 2-aryl-4H-benzo[d][1,3]oxazine-4-carboxylate in good yields. In addition, 2-diazo-2-(2-arylthioamidophenyl)acetate affords the corresponding 2-aryl-4H-benzo[d][1,3]thiazine derivatives under similar conditions. This is the first example of the synthesis of benzoxazines and benzothiazines from ortho-amidophenyl diazoacetate and ortho-thioamidophenyl diazoacetate, respectively.
机译:使用催化量的三氟甲磺酸铜在温和条件下产生2-芳基-4H-苯并[d] [1,3]恶嗪-4-化合物,可以实现2-(2-芳基氨基苯基)-2-重氮乙酸酯的分子内CO插入。羧酸盐收率高。另外,在相似条件下,2-重氮-2-(2-芳基硫代酰胺基苯基)乙酸酯提供相应的2-芳基-4H-苯并[d] [1,3]噻嗪衍生物。这是分别由邻氨基酰胺基苯基重氮乙酸酯和邻硫代氨基酰胺基苯基重氮乙酸酯合成苯并恶嗪和苯并噻嗪的第一个实例。

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