首页> 外文期刊>Journal of Heterocyclic Chemistry: The International Journal of Heterocyclic Chemistry >Reinvestigation of Alternative Method for the Preparation of Dibenz[bf][1,4]oxazepine
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Reinvestigation of Alternative Method for the Preparation of Dibenz[bf][1,4]oxazepine

机译:制备地苯并[bf] [1,4]奥沙西平的替代方法的再研究

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摘要

Two distinct alternative methods using different starting materials for the preparation of dibenz[bf] [1,4]oxazepine (7, CR) were reinvestigated. The possibility of trans-cis conversion of the Schiff base 5 (produced from 1 and 2) is considered the favorable orientation that leads to cyclization (production of 7). Fluoro derivative of I afforded excellent and more convenient conditions for the one pot preparation of high yield pure 7. The presence of only trans configurafion for the imine 6 (produced from 3 with 4) and the impossibility of its conversion to cis, makes it inadequate for the preparation of 7.
机译:对使用不同原料制备地苯并[bf] [1,4]奥氮平(7,CR)的两种不同方法进行了重新研究。 Schiff碱5(由1和2产生)的反式顺式转化的可能性被认为是导致环化(产生7)的有利取向。 I的氟代衍生物为一锅高纯度纯7的制备提供了极佳且更方便的条件。亚胺6(仅由3加4生成)仅具有反式构型,并且无法将其转化为顺式,因此不足。用于准备7。

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