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首页> 外文期刊>Journal of Heterocyclic Chemistry: The International Journal of Heterocyclic Chemistry >Efficient synthesis and spectral determination of 11-[(o-; m-; and p-substituted)-phenyl]-8-chloro-3,3-dimethyl-2,3,4,5,10,11-hexahydro-1H-dibenzo[b,e][1,4]diazepin-1-ones
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Efficient synthesis and spectral determination of 11-[(o-; m-; and p-substituted)-phenyl]-8-chloro-3,3-dimethyl-2,3,4,5,10,11-hexahydro-1H-dibenzo[b,e][1,4]diazepin-1-ones

机译:11-[(o-; m-;和p-取代的)-苯基] -8-氯-3,3-二甲基-2,3,4,5,10,11-六氢-1H的高效合成和光谱测定-二苯并[b,e] [1,4]二氮杂-1-酮

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摘要

A new synthesis to obtain eleven novel derivatives of 11-[(o-; m-; and p-substituted)-phenyl]-8-chloro-3,3-dimethyl-2,3,4,5, 10,11-hexahydro-1H-dibenzo[b,e][1,4]diazepin-1-ones with possible pharmacological activity in the central nervous system in two efficient steps has been developed. The final products were obtained by condensation and cyclization between 3-[4-chloro-1,2-phenylenediamine]-5,5-dimethyl-2-cyclohexenone with (o-; m-; and p-substituted)benzaldehyde. The structure of all products was corroborated by ir, H-1-nmr, C-13-nmr and high resolution in ms.
机译:获得11-[(o-; m-;和p-取代的)-苯基] -8-氯-3,3-二甲基-2,3,4,5,10,11-的11种新衍生物的新合成方法已经开发出在两个有效步骤中在中枢神经系统中具有可能的药理活性的六氢-1H-二苯并[b,e] [1,4]二氮杂-1-酮。通过在3- [4-氯-1,2-苯二胺] -5,5-二甲基-2-环己烯酮与(邻-;间-和对-取代)苯甲醛之间缩合和环化获得最终产物。 ir,H-1-nmr,C-13-nmr和以ms为单位的高分辨率证实了所有产品的结构。

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