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首页> 外文期刊>Der Pharma Chemica: journal for medicinal chemistry, pharmaceutical chemistry and computational chemistry >Synthesis of 6-Aryl Substituted Derivatives of 6-Bromo-8-Methyl-1, 11-Diazabenzo[A]Phenothiazin-5-One Via Palladium Catalyzed Suzuki Coupling Reaction
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Synthesis of 6-Aryl Substituted Derivatives of 6-Bromo-8-Methyl-1, 11-Diazabenzo[A]Phenothiazin-5-One Via Palladium Catalyzed Suzuki Coupling Reaction

机译:钯催化的铃木偶联反应合成6-溴-8-甲基-1,11-重氮苯并[A]吩噻嗪-5-一的6-芳基取代衍生物

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摘要

The synthesis of 6-substituted aryl derivatives of 8-methyl-1,11-diazabenzo[a]phenothiazin-5-one, potential vat dyes is reported. This was achieved by condensation reaction between 2-amino-4-methylpyridine-3-thiol and 6,7-dibromo-5,8-quinolinequinone under anhydrous basic condition to obtain 6-bromo-8-methyl-1,11-diazabenzo[a]phenothiazin-5-one as the parent compound. The 6-aryl derivatives of this parent compound were obtained using Suzuki-Miyaura protocol. The structure of the synthesized compounds was established by spectra and analytical data obtained. These compounds showed great potentials as vat dyes.
机译:据报道,合成了8-甲基-1,11-二氮杂苯并[a]吩噻嗪-5-一个潜在的还原染料的6-取代的芳基衍生物。这是通过在无水碱性条件下使2-氨基-4-甲基吡啶-3-硫醇与6,7-二溴-5,8-喹啉醌缩合反应而获得的6-溴-8-甲基-1,11-二氮杂苯并[ a]吩噻嗪-5-酮作为母体化合物。使用Suzuki-Miyaura方案获得该母体化合物的6-芳基衍生物。通过光谱和获得的分析数据确定了合成化合物的结构。这些化合物具有还原染料的巨大潜力。

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