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首页> 外文期刊>Journal of Heterocyclic Chemistry: The International Journal of Heterocyclic Chemistry >CONVENIENT SYNTHESIS OF 6-SUBSTITUTED-2-CHLORO-5,12-DIHYDRO-5-OXOBENZOXAZOLO[3,2-A]QUINOLINES AND N-ACYLATED-3-CHLORODIBENZ[B,E][1,4]OXAZEPIN-11(5H)-ONES
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CONVENIENT SYNTHESIS OF 6-SUBSTITUTED-2-CHLORO-5,12-DIHYDRO-5-OXOBENZOXAZOLO[3,2-A]QUINOLINES AND N-ACYLATED-3-CHLORODIBENZ[B,E][1,4]OXAZEPIN-11(5H)-ONES

机译:便捷合成6-取代的2-氯-5,12-二氢-5-氧杂苯并恶唑啉[3,2-A]喹啉和N-酰化的3-氯二苯[B,E] [1,4]恶唑啉-11( 5H)-ONES

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Convenient synthesis of variously substituted 2-chloro-5,12-dihydro-5-oxobenzoxazolo[3,2-a]quinolnes at the 6-position and N-acylated-3-chlorodibenz[b,e][1,4]oxazepin-11(5H)-ones are reported. The former compounds were obtained in 65-93% yield by simply heating N-acyl-4-chloro-N-(2-hydroxyphenyl)anthranilic acids in acetic anhydride for 4 hours, and the latter by heating sodium salt of N-acyl-4-chloro-N-(2-hydroxyphenyl)anthranilic acids with acetic anhydride. [References: 3]
机译:方便地合成6-位不同取代的2-氯-5,12-二氢-5-氧代苯并恶唑并[3,2-a]喹诺酮和N-酰化-3-氯二苯并[b,e] [1,4]恶唑啉报告了-11(5H)-一个。前者通过简单地将N-酰基-4-氯-N-(2-羟基苯基)邻氨基苯甲酸在乙酸酐中加热4小时,以65-93%的产率制得,而后者通过加热N-酰基-N的钠盐获得。 4-氯-N-(2-羟基苯基)邻氨基苯甲酸与乙酸酐。 [参考:3]

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