Experimental Design-Based Response Surface Methodology Optimization for Synthesis of β-Mercapto Carbonyl Derivatives as Antimycobacterial Drugs Catalyzed by Calcium Pyrophosphate.

International Journal of Medicinal Chemistry Pub Date : 2014-01-01 Epub Date: 2014-03-06 DOI:10.1155/2014/586437
Younes Abrouki, Abdelkader Anouzla, Hayat Loukili, Jamal Bennazha, Rabiaâ Lotfi, Ahmed Rayadh, My Abdellah Bahlaoui, Saïd Sebti, Driss Zakarya, Mohamed Zahouily
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引用次数: 4

Abstract

A simple protocol for the efficient preparation of β-mercapto carbonyl derivatives as antimycobacterial drugs has been achieved via Thia-Michael reaction between chalcones derivatives and thiols in the presence of calcium pyrophosphate as a heterogeneous catalyst under mild reaction conditions. The central composite design was used to design an experimental program to provide data to model the effects of various factors on reaction yield (Y). The variables chosen were catalyst weight (X 1), reaction time (X 2), and solvent volume (X 3). The mathematical relationship of reaction yield on the three significant independent variables can be approximated by a nonlinear polynomial model. Predicted values were found to be in good agreement with experimental values. The optimum reaction conditions for reaction model (chalcone and thiophenol) obtained by response surface were applied to other substrates. This procedure provides several advantages such as high yield, clean product formation, and short reaction time.

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基于实验设计的响应面法优化焦磷酸钙催化合成抗真菌药物β-巯基羰基衍生物。
以焦磷酸钙为非均相催化剂,在温和反应条件下,查尔酮衍生物与硫醇进行Thia-Michael反应,获得了一种高效制备β-巯基衍生物抗真菌药物的简单方案。采用中心复合设计设计实验方案,提供数据来模拟各种因素对反应产率(Y)的影响。选择的变量为催化剂重量(x1)、反应时间(x2)和溶剂体积(x3)。反应产率在三个重要自变量之间的数学关系可以用非线性多项式模型近似。结果表明,预测值与实验值吻合良好。通过响应面得到的反应模型(查尔酮和噻吩)的最佳反应条件应用于其他底物。该工艺具有收率高、产物形成干净、反应时间短等优点。
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期刊介绍: International Journal of Medicinal Chemistry is a peer-reviewed, Open Access journal that publishes original research articles as well as review articles in all areas of chemistry associated with drug discovery, design, and synthesis. International Journal of Medicinal Chemistry is a peer-reviewed, Open Access journal that publishes original research articles as well as review articles in all areas of chemistry associated with drug discovery, design, and synthesis.
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