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A Novel and Expedient Approach to New Heterocycles Containing Benzothiophene, Benzothieno[2,3-d]pyrimidine and Coumarin Moieties

机译:一种新颖且简便的方法,用于处理含有苯并噻吩,苯并噻吩并[2,3-d]嘧啶和香豆素部分的新杂环

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摘要

In order to obtain potent protein-tyrosine kinase inhibitors, a novel and versatile method for synthesis of heterocyclic compounds 4a-d and 5a-c comprising 2-imino-2H-1-benzopyran, tetrahydrobenzo[b]thiophene, and carboxamide/1H-benzimidazole fragments has been developed. This method was based on the reactions of 2-imino-2H-1-benzopyrans 1a,b and 2 with 2-amino-4,5,6,7-tetrahydrobenzo[b]thiophenes 3a-c in glacial acetic acid. Furthermore, new heterocycles 8a,b with tetrahydrobenzo[4,5]thieno[2,3-d]pyrimidine and coumarin moieties have been synthesized via a rearrangement of the corresponding 2-(tetrahydrobenzo[b]thien-2-yl)imino-2H-1-benzopyran-3-carboxamides 4a,b.
机译:为了获得有效的蛋白酪氨酸激酶抑制剂,一种新颖且通用的合成杂环化合物4a-d和5a-c的方法,该化合物包括2-亚氨基-2H-1-苯并吡喃,四氢苯并[b]噻吩和羧酰胺/ 1H-已开发出苯并咪唑片段。该方法基于2-亚氨基-2H-1-苯并吡喃1a,b和2与2-氨基-4,5,6,7-四氢苯并[b]噻吩3a-c在冰醋酸中的反应。此外,已经通过相应的2-(四氢苯并[b]噻吩-2-基)亚氨基-的重排合成了具有四氢苯并[4,5]噻吩并[2,3-d]嘧啶和香豆素部分的新杂环8a,b。 2H-1-苯并吡喃-3-羧酰胺4a,b。

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