New phosphorus-containing polycycles with a spiroamine group

Grygorii M. Koidan, A. Marchenko, Anastasiia M. Hurieva, Aleksandr M. Kostyuk
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Abstract

Aim. To synthesize hexahydrospiro[cyclopropane-1,10’-pyrido[1,2-c]quinazoline] and 2-λ5-benzo[f][1,4,2]diazaphosphepine derivatives – new N-P containing heterocyclic compounds with the 6-azaspiro[2.5]octane fragment.Results and discussion. A new analog of the powerful electrophilic reagent – “Alder dimer” ‒ was obtained from the interaction of triflic anhydride and spiro(4-cyclopropane) piperidinyl formamide, and further used to synthesize new Nʹ-PV- and PIII-substituted Νʹ-phenyl, Νʹʹ-hexahydro(azaspiro)octylformamidinium salts – precursors of acyclic N-phosphorylated diamino carbenes with a spiroamine group. It has been shown that acyclic N-phosphorylated diaminocarbenes are transient species affording various products. The structure of the final product is primarily determined by nature of the phosphorus-bearing substituent, namely a phosphoryl or phosphino-group. N-PV-substituted carbene undergoes a 1,2-phosphorus shift with the formation of (selenophosphoryl)formamidine in a high yield. For N-PIII-substituted carbene a compatible 1,3-H shift also occurs with the formation of an intermediate azomethine ylide converted into a new heterocyclic system – hexahydrospirocyclopropane -1,10’-pyrido[1,2-c]quinazoline. Under the action of acid an unexpected further expansion of the 6-member ring occurs with the formation of a diazepine derivative.Experimental part. The reaction of Alder reagent with N-PV-seleno phosphoryl arylamides afforded N-phosphorus substituted formamidinium salts, which are easily reduced to PIII analogues. In addition to the corresponding formamidines, the new N-phosphorylated spiroamine-containing polycyclic system was isolated from the reaction mixture formed by the deprotonation of such salts with a strong non-nucleophilic base.Conclusions. The Alder reagent approach allows synthesizing precursors of acyclic formamidine carbenes with the spiroamine group. Such carbenes are unstable. By converting these compounds N-PIII-substituted tetrahydropyrimidine and diazaphosphepine derivatives with the 6-azaspiro[2.5]octane fragment have been obtained for the first time.
含螺胺基的新型含磷多环化合物
的目标。合成六氢螺[环丙烷-1,10 ' -吡啶[1,2-c]喹唑啉]和2-λ5-苯并[f][1,4,2]重氮膦衍生物-含6-氮杂环化合物[2.5]辛烷片段。结果和讨论。通过三酸酐与螺(4-环丙烷)胡椒酰甲酰胺的相互作用,得到了一种新的亲电试剂“Alder二聚体”,并进一步用于合成新的N′- pv -和piii -取代Ν′-苯基,Ν′′-六氢(azspiro)辛基甲酰胺盐-含螺胺基的无环N-磷酸化二氨基苯的前体。研究表明,无环n -磷酸化二氨基碳烯是一种瞬态物质,可产生多种产物。最终产物的结构主要取决于含磷取代基的性质,即磷基或磷酸基。n - pv取代的碳烯发生1,2-磷位移,生成(硒磷酰基)甲脒,收率高。对于n - piii -取代的羰基,随着中间亚甲基酰基转化为新的杂环体系-六氢螺环丙烷-1,10 ' -吡啶[1,2-c]喹唑啉的形成,相容的1,3- h移位也发生了。在酸的作用下,六元环意外地进一步膨胀,形成了二氮卓衍生物。实验部分。Alder试剂与n - pv -硒磷酰芳酰胺反应生成n -磷取代的甲脒盐,该盐易于还原为PIII类似物。除了相应的甲脒外,还从这些盐与强非亲核碱脱质子形成的反应混合物中分离出新的n-磷酸化含螺胺的多环体系。Alder试剂方法允许合成具有螺胺基的无环甲脒碳烯的前体。这种碳烯是不稳定的。通过将这些化合物n - piii取代的四氢嘧啶和二氮膦衍生物与6-氮杂螺[2.5]辛烷值片段进行转化,首次得到了这些化合物。
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