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Synthesis of 2-((4-Substituted Phenyl) Amino) Benzaldehyde

机译:合成2 - ((4-取代的苯基)氨基)苯甲醛

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摘要

2-((4-substituted phenyl) amino) benzaldehyde, is an important intermediate for the synthesis of many biologically active intermediates of anticancer drugs. In this work, a rapid and high efficiency synthetic method for compound 1a-1b was established. Compound 1a-1b was synthesized from 2-chloronicotinic acid and 4-substituted anilines through three steps including nucleophilic substitution, reduction and oxidation reaction. The structure of the target compound 1a-1b was confirmed by H NMR and MS spectrum. Furthermore, the synthetic method was optimized. The total yield of the three steps was 59.49%.
机译:2 - ((4-取代的苯基)氨基)苯甲醛,是合成抗癌药物许多生物活性中间体的重要中间中间体。在这项工作中,建立了一种快速和高效的化合物1A-1B的合成方法。通过包括亲核取代,还原和氧化反应的三个步骤,通过三个步骤合成化合物1A-1B。通过H NMR和MS光谱证实了目标化合物1A-1B的结构。此外,优化了合成方法。三个步骤的总产量为59.49%。

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