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首页> 外文期刊>Synlett >First Synthesis of 2,9-Disubstituted cis-2,3a,7b,9,10a,14b-Hexaazaperhydrodibenzotetracenes
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First Synthesis of 2,9-Disubstituted cis-2,3a,7b,9,10a,14b-Hexaazaperhydrodibenzotetracenes

机译:第一次合成2,9-二取代的顺式-2,3a,7b,9,10a,14b-六己唑氢二苯并丙烯

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摘要

The first synthesis of 2,9-disubstituted cis -2,3а,7b,9,10a,14b-hexaazaperhydrodibenzotetracenes has been accomplished through intermolecular heterocyclization of N , N -bis(methoxymethyl)alkylamines with cis -1,6,7,12-tetraazaperhydrotetracene in the presence of SmCl_(3)·6H_(2)O catalyst or by recyclization of 1,3,5-tricycloalkyl-1,3,5-triazinanes with cis -1,6,7,12-tetraazaperhydrotetracene in the presence of NiCl_(2)·6H_(2)O catalyst. The structures were established by 1D (~(1)H, and ~(13)C) and 2D (HSQC, HMBC, COSY, NOESY) NMR spectroscopy, MALDI TOF/TOF mass spectrometry, and X-ray diffraction analyses.
机译:通过N,N-BIS(甲氧基甲基)烷基胺的分子间杂核来实现,通过N,N-1,6,7,12的分子杂环化完成了2,9-二取代的顺式-2,3和7B,9,10A,14B-六己酰磺酰氯苯乙烯酮已经完成 - 在SMCl_(3)·6H_(2)o催化剂存在下或通过用CIS -1,6,7,12-四唑氢酰胺的1,3,5-三环烷基-1,3,5-三氮烷的再循环中的脱氧哌啶苯乙烯 NiCl_(2)·6H_(2)o催化剂的存在。 该结构由1D(〜(1)小时,〜(13)c)和2D(HSQC,HMBC,Cozy,Noesy)NMR光谱,MALDI TOF / TOF质谱和X射线衍射分析建立。

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