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Method of manufacturing the new wilderness e indole

机译:新荒地[e]吲哚的制造方法

摘要

The areno(e)indols have the formula (I). The methods comprises: (a) reacting (VI) with a strong base and thereafter with an aldehyde Ar'-CHO to obtain (VII); (b) oxidizing (VII) to yield the cetone (VIII); (c) reating (VIII) with a strong base and thereafter with an acyle chloride ClCOR, to produce (IX); (d) subjecting to a photochemical cyclization (IX) to produce (I). In said formulas Ar is phenyl or substituted phenyl; Ar' is a radical (i) or (ii); R is an acyle group, Ar' is a phenyl, pyrolyl, furanyl or thiophenyl group substituted up to three times by any of the radicals R, R?1, R2, or R3¿. The compounds (I) are useful as intermediates in the synthesis of hexahydroareno(e)cyclopropa(c)indol-4-ones with antitumoral activity.
机译:芳族吲哚具有式(I)。该方法包括:(a)使(VI)与强碱反应,然后与醛Ar'-CHO反应,得到(VII); (b)氧化(VII)得到丙酮(VIII); (c)用强碱处理(VIII),然后用酰氯ClCOR处理,得到(IX); (d)进行光化学环化(IX)以产生(I)。在所述式中,Ar是苯基或取代的苯基; Ar'是基团(i)或(ii); R为酰基,Ar'为苯基,吡咯基,呋喃基或硫代苯基,最多被基团R,R 1,R 2或R 3-中的任何一个取代三倍。化合物(I)可用作合成具有抗肿瘤活性的六氢芳基(e)环丙(c)吲哚-4-酮的中间体。

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