首页> 外文期刊>Journal of Heterocyclic Chemistry: The International Journal of Heterocyclic Chemistry >Synthesis of 5H-1,2,3-triazolo[4,3-a][2]benzazepines from the Baylis-Hillman adducts of 2-alkynylbenzaldehydes
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Synthesis of 5H-1,2,3-triazolo[4,3-a][2]benzazepines from the Baylis-Hillman adducts of 2-alkynylbenzaldehydes

机译:从2-炔基苯甲醛的Baylis-Hillman加合物合成5H-1,2,3-三唑并[4,3-a] [2]苯并ze庚因

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摘要

The facile synthesis of 5H-1,2,3-triazolo[4,3-a][2]benzazepines 5a-d by the intramolecular 1,3-dipolar cycloaddition reaction of 2-alkynylphenylallyl azides 4a-d is described. The latter were readily obtained from 2-alkynylbenzaldehydes 1a-d through the Baylis-Hillman adducts 2a-d followed by acetylation to compounds 3a-d and nucleophilic substitution by azide to compounds 4a-d.
机译:描述了通过2-炔基苯基烯丙基叠氮化物4a-d的分子内1,3-偶极环加成反应容易地合成5H-1,2,3-三唑并[4,3-a] [2]苯并ze庚因5a-d。后者可容易地从2-炔基苯甲醛1a-d通过Baylis-Hillman加合物2a-d获得,然后乙酰化为化合物3a-d,并通过叠氮化物亲核取代为化合物4a-d。

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