首页> 外文期刊>Heterocycles: An International Journal for Reviews and Communications in Heterocyclic Chemistry >A NEW SYNTHETIC APPROACH TO PENTACYCLIC RING, 6,7,14,15-TETRAHYDRO[1,5]DIAZOCINO[1,2-a:6,5-a']-8-DIHYDRODHNDOLE
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A NEW SYNTHETIC APPROACH TO PENTACYCLIC RING, 6,7,14,15-TETRAHYDRO[1,5]DIAZOCINO[1,2-a:6,5-a']-8-DIHYDRODHNDOLE

机译:五环[6,7,14,15-四氢[1,5]重氮[1,2-a:6,5-a']-8-二氢吲哚的五环新合成方法

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摘要

The construction of a new pentacyclic ring system, 6,7,14,15-tetrahydro[1,5]diazocino[1,2-a:6,5-a']-8-dihydrodiindole (7) from simple precursors through our new synthetic route was presented to be a facile and concise method for an intramolecular N-alkylation of tosylate 12 which was obtained from N-acylation of indoline 4 with indole acid 9, followed by reduction and tosylation. This new synthetic approach can overcome the disadvantage of uncontrollable intermolecular double N-alkylation of the precursor 3 to produce the unexpected ring system 2.
机译:通过简单的前体,通过我们的前驱体构建新的五环系统,即6,7,14,15-四氢[1,5]重氮[1,2-a:6,5-a']-8-二氢二吲哚(7)提出了一种新的合成路线,该路线为甲苯磺酸酯12的分子内N-烷基化的简便方法,该方法是将吲哚4与吲哚酸9进行N-酰化,然后进行还原和甲苯磺酸化。这种新的合成方法可以克服前体3不可控制的分子间双N-烷基化以产生意想不到的环系统2的缺点。

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