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首页> 外文期刊>Green Chemistry Letters and Reviews >Green synthesis of novel (E)-2-(1,4-dioxo-1,2,3,4-tetrahydrophthalazine-2-carbonyl)-3-(1H-indol-3-yl)acrylonitriles
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Green synthesis of novel (E)-2-(1,4-dioxo-1,2,3,4-tetrahydrophthalazine-2-carbonyl)-3-(1H-indol-3-yl)acrylonitriles

机译:绿色合成新型(E)-2-(1,4-二氧-1,2,3,4-四氢酞嗪-2-羰基)-3-(1H-吲哚-3-基)丙烯腈

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Green synthesis of novel title compounds (6) has been developed from 3-(1,4-dioxo-3,4-dihydrophthalazin-(1H)-yl)-3-oxopropanenitrile (3) and indole-3-aldehyde (4) using Knoevenagel condensation followed by alkylation with alkylating agents. Compound 6 could also be synthesised by alkylation of 4 followed by condensation with 3. In an alternate sequence of reactions, 6 could be synthesised either from treatment of 3 with N,N-dimethylformamide dimethyl acetal to form (E)-3-(dimethlamino)-2-(1,4-dioxo-1,2,3,4-tetrahydrophthalazine-2-carbonyl)acrylonitrile 8 followed by reaction with 10 or by the reaction 8 with 9 followed by alkylation.
机译:从3-(1,4-dioxo-3,4-dihydrophthalazin-((1H)-yl)-3-氧代丙烷腈(3)和吲哚-3-醛(4)开发了新型标题化合物(6)的绿色合成方法使用Knoevenagel缩合,然后用烷基化剂进行烷基化。化合物6也可以通过将4烷基化,然后与3缩合来合成。在另一种反应顺序中,可以通过用N,N-二甲基甲酰胺二甲基乙缩醛处理3形成(E)-3-(dimethlamino)来合成6 )-2-(1,4-二氧代-1,2,3,4-四氢酞嗪-2-羰基)丙烯腈8,然后与10或与8的反应8,再进行烷基化。

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