首页> 外文期刊>Journal of Heterocyclic Chemistry: The International Journal of Heterocyclic Chemistry >Reactions of 3-benzylindole-2-carbohydrazides: Synthesis of new 10-benzyl-1,2-dihydro-1-oxo-1,2,4-triazino[4,5-a]indoles and 3-benzyl-2-(1,3,4-oxadiazol-2-yl)indoles
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Reactions of 3-benzylindole-2-carbohydrazides: Synthesis of new 10-benzyl-1,2-dihydro-1-oxo-1,2,4-triazino[4,5-a]indoles and 3-benzyl-2-(1,3,4-oxadiazol-2-yl)indoles

机译:3-苄基吲哚-2-碳酰肼的反应:合成新的10-苄基-1,2-二氢-1-氧代-1,2,4-三嗪基[4,5-a]吲哚和3-苄基-2-( 1,3,4-恶二唑-2-基)吲哚

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摘要

3-Benzylindole-2-carbohydrazides (4) on reaction with triethylorthoformate in a polar solvent like DMF yielded only 10-benzyl-1,2-dihydro-1-oxo-1,2,4-triazino[4,5-a]indoles (5) while (4) on reaction with triethylorthoacetate in DMF yielded both 10-benzyl-4-methyl-1,2-dihydro-1-oxo-1,2,4-triazino[4,5-a]indoles (5) and 3-benzyl-2-(5-methyl-1,3,4-oxadiazol-2-yl)indoles (6) instead of only the triazinoindoles as expected. The oxadiazolylindoles (6) were also synthesized by refluxing (4) with excess of orthoesters. The structures of the compounds formed were characterized by their analytical and spectral data. [References: 10]
机译:3-苄基吲哚-2-碳酰肼(4)在极性溶剂(如DMF)中与原甲酸三乙酯反应生成仅10-苄基-1,2-二氢-1-氧-1,2,4-三嗪[4,5-a]吲哚(5)与(4)在DMF中与原乙酸三乙酯反应生成10-苄基-4-甲基-1,2-二氢-1-氧代-1,2,4-三嗪基[4,5-a]吲哚( 5)和3-苄基-2-(5-甲基-1,3,4-恶二唑-2-基)吲哚(6)而不是仅预期的三嗪并吲哚。还通过与过量的原酸酯回流(4)来合成恶二唑基羟吲哚(6)。形成的化合物的结构通过其分析和光谱数据表征。 [参考:10]

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