首页> 外国专利> METHOD OF PRODUCING ALKYL 2-SUBSTITUTED 6H-BENZOTHIENO2,3,4-ij-2,7-NAPHTHYRIDINE-5-CARBOXYLATES

METHOD OF PRODUCING ALKYL 2-SUBSTITUTED 6H-BENZOTHIENO2,3,4-ij-2,7-NAPHTHYRIDINE-5-CARBOXYLATES

机译:烷基2-取代的6H-苯并噻吩并[2,3,4-ij] -2,7-萘啶-5-羧酸酯的制备方法

摘要

FIELD: chemistry.;SUBSTANCE: invention relates to a method of producing alkyl 2-substituted 6H-benzothieno[2,3,4-ij]-2,7-naphthyridine-5-carboxylates of general formula 1 , where 1a Ar=Ph, R=H, R′=Et; 1b Ar=4-CH3O-C6H4, R=CH3, R'=Et; 1c Ar=4-CH3-C6H4, R=CH3, R'=Am; 1d Ar=4-CH3-C6H4, R=CH3O, R'=Et; 1e Ar=Ph, R=H, R'=Am, which can be used as potentially biologically active substances and semi-products for synthesis of novel heterocyclic systems. The method of producing alkyl 2-substituted 6H-benzothieno[2,3,4-ij]-2,7-naphthyridine-5-carboxylates of general formula I includes forming a heterocyclic system of 6H-benzothieno[2,3,4-ij]-2,7-naphthyridine as a result of thermal decomposition of the azido group of alkyl 3-azidothieno[2,3-b]pyridine-2-carboxylates and intramolecular cyclisation of the formed nitrene; the reaction is carried out while boiling said compounds in chlorobenzene for 30-60 minutes.;EFFECT: high output.;3 tbl, 6 ex
机译:技术领域本发明涉及制备通式1的烷基2-取代的6H-苯并噻吩并[2,3,4-ij] -2,7-萘啶-5-羧酸酯的方法。,其中1a Ar = Ph,R = H,R′= Et; 1b Ar = 4-CH 3 O-C 6 H 4 ,R = CH 3 ,R'= Et; 1c Ar = 4-CH 3 -C 6 H 4 ,R = CH 3 ,R'= Am ; 1d Ar = 4-CH 3 -C 6 H 4 ,R = CH 3 O,R'=等等1e Ar = Ph,R = H,R'= Am,可用作合成新杂环系统的潜在生物活性物质和半成品。制备通式I的烷基2-取代的6H-苯并噻吩并[2,3,4-ij] -2,7-萘啶-5-羧酸酯的方法包括形成6H-苯并噻吩并[2,3,4-的杂环系统ij] -2,7-萘啶是由3-叠氮基[2,3-b]吡啶-2-羧酸烷基酯的叠氮基热分解和所形成的腈的分子内环化的结果。反应在将所述化合物在氯苯中沸腾30-60分钟的同时进行。效果:高产量。3tbl,6 ex

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