Synthesis of some new bis(pyrazol-5-ols), pyridones and benzo-[f]-thiochromene-2-carbonitrile derivatives bearing N-(4-chlorophenyl)-2-(4-formylphenoxy)acetamide moiety

Mahmoud Arafat, Ehab Khalifa, F. El‐Taweel, S. Ayyad, K. Mohamed
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Abstract

Novel 4,4′-(arylmethylene)-bis(3-methyl-1-phenyl-1 H -pyrazol-5-ol) derivative 2 was synthesized via interaction of N -(4-chlorophenyl)-2-(4-formylphenoxy)acetamide ( 1 ) with diverse available reagent (two mole from 3-methyl-1H-pyrazol-5(4 H )-one). Moreover, One-pot pseudo three-component reaction of hydrazine hydrate, ethyl acetoacetate and aldehydes in ethanole using pipridine at 70°C afforded the corresponding aminopyrazole derivative 3 . on the other hand, cyanoacetamide scaffolds 4a,b was reacted with aromatic aldehyde particularly N -(4-chlorophenyl)-2-(4-formylphenoxy)acetamide ( 1 ), to afford arylidenes 5a,b that undergoes cyclization by heating in ethanol containing drops of piperidine as catalyst, and malononitrile afforded the corresponding pyridinone derivatives 6a,b . All freshly synthesized scaffolds were elucidated by considering the data of both elemental and spectral analyses.
一些新的双(吡唑-5-醇)、吡啶酮和含N-(4-氯苯基)-2-(4-甲酰苯氧基)乙酰胺的苯并[f]-硫代铬-2-碳腈衍生物的合成
通过N -(4-氯苯基)-2-(4-甲酰基苯氧基)乙酰胺(1)与多种可用试剂(3-甲基- 1h -吡唑-5(4 H)- 1两摩尔)的相互作用,合成了新的4,4′-(芳基亚甲基)-双(3-甲基-1-苯基-1H-吡唑-5-醇)衍生物2。在70℃条件下,用哌啶在乙醇中对水合肼、乙酰乙酸乙酯和醛类进行一锅伪三组分反应,得到相应的氨基吡唑衍生物3。另一方面,氰乙酰胺支架4a,b与芳香醛特别是N -(4-氯苯基)-2-(4-甲酰基苯氧基)乙酰胺(1)反应生成芳基烯5a,b,在含哌啶滴剂的乙醇中加热生成环化,丙二腈生成相应的吡啶酮衍生物6a,b。通过元素分析和光谱分析对新合成的支架进行了鉴定。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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