Nezhad Shefa Mirani, Pourmousavi Seied Ali, Zare Ehsan Nazarzadeh
School of Chemistry, Damghan University, Damghan, 36716-41167, Iran.
Curr Org Synth. 2022 Mar 3;19(2):246-266. doi: 10.2174/1570179418666211104143736.
The use of polymer-based catalysts has increased because of their high potential application as an effective catalyst in organic reactions. They have benefits such as high efficiency and reactivity, simple separation, and safety compared to other heterogeneous catalysts.
The objective of the current research is to prepare solid polymer-based catalysts, poly(aniline-co-m-phenylenediamine) (PAmPDA), and its superparamagnetic nanocomposite. Then, the catalytic activity of the resulting superparamagnetic nanocomposite was investigated in the synthesis of 1H-pyrazolo[1,2-b]phetalazine-5,10-diones and 1H-pyrazolo[1,2-a]pyridazine-5,8-dione derivatives. A series of some 1H-pyrazolo[1,2-b]phetalazine-5,10-diones and 1H-pyrazolo[1,2-a]pyridazine-5,8-dione derivatives was tested for its antibacterial properties against the Staphylococcus aureus and E. coli bacteria.
PAmPDA copolymer was synthesized in a 1:2 molar ratio of Ani to mPDA via radical oxidative polymerization at room temperature. Superparamagnetic PAmPDA@FeOnanocompo-site was synthesized from a mixture of Fe(II), Fe(III) solution, and PAmPDA copolymer via the in-situ co-precipitation technique. 1H-pyrazolo[1,2-b]phetalazine-5,10-diones were synthesized via one-pot three-component condensation reaction of Phthalhydrazide, aromatic aldehyde derivatives, and malono-nitrile in the presence of PAmPDA under solvent-free conditions at 80 °C. The synthesis of 1H-pyrazolo[1,2-a]pyridazine-5,8-dione derivatives was carried out via a one-pot three-component condensa-tion reaction of maleic hydrazide, aromatic aldehyde derivatives, and malononitrile in the presence of PAmPDA under reflux conditions at EtOH/H2O 1:1. The antibacterial activity of some derivatives was tested against Gram-positive and Gram-negative bacteria.
First, superparamagnetic PAmPDA@FeO nanocomposite was synthesized and characterized successfully, and then the resulting nanocatalyst was used for the synthesis of pyrazolo[1,2-b]phthalazine and pyrazolo[1,2-a]pyridazine. We obtained the maximum yield of the desired 1H-pyrazolo[1,2-b]phthalazine-5,10 dione derivatives with 0.05 g of catalyst at 80°C, under solvent free conditions, whereby the reaction was complete within 30 min. A wide range of 1H-pyrazolo[1,2-b]phthalazine-5,10 dione derivatives were synthesized in good to excellent yield. On the other hand, pyrazolo[1,2-a]pyridazine derivative was synthesized successfully in high yield using PAmPDA as a nanocatalyst. The antibacterial activity of some derivatives, according to the data (inhibition zone%), showed good ac-tivity against Staphylococcus aureus and E. coli.
In this research, PAmPDA was used for mild preparation of 1H-pyrazolo [1,2-a]pyridazine-5,8-diones & 1H-pyrazolo[1,2-b]phetalazine-5,10-diones derivatives with excellent yields and short reac-tion times. The attractive features of this protocol are simple procedure, cleaner reaction, and the use of recyclable nanocatalyst. Satisfactory yields of products and easy workup make this a useful protocol for the green synthesis of this class of compounds. The antibacterial activity of some derivatives, according to the data (inhibition zone%), showed good activity against Staphylococcus aureus and E. coli.
基于聚合物的催化剂因其在有机反应中作为有效催化剂具有很高的潜在应用价值而得到越来越广泛的使用。与其他非均相催化剂相比,它们具有诸如高效、高反应活性、易于分离和安全等优点。
本研究的目的是制备基于固体聚合物的催化剂聚(苯胺 - 间苯二胺)(PAmPDA)及其超顺磁性纳米复合材料。然后,研究所得超顺磁性纳米复合材料在合成1H - 吡唑并[1,2 - b]酞嗪 - 5,10 - 二酮和1H - 吡唑并[1,2 - a]哒嗪 - 5,8 - 二酮衍生物中的催化活性。测试了一系列1H - 吡唑并[1,2 - b]酞嗪 - 5,10 - 二酮和1H - 吡唑并[1,2 - a]哒嗪 - 5,8 - 二酮衍生物对金黄色葡萄球菌和大肠杆菌的抗菌性能。
通过在室温下进行自由基氧化聚合反应,以1:2的Ani与mPDA摩尔比合成PAmPDA共聚物。通过原位共沉淀技术,由Fe(II)、Fe(III)溶液和PAmPDA共聚物的混合物合成超顺磁性PAmPDA@FeO纳米复合材料。在无溶剂条件下,于80°C,在PAmPDA存在下,通过邻苯二甲酰肼、芳族醛衍生物和丙二腈的一锅三组分缩合反应合成1H - 吡唑并[1,2 - b]酞嗪 - 5,10 - 二酮。在乙醇/水1:1回流条件下,在PAmPDA存在下,通过马来酰肼、芳族醛衍生物和丙二腈的一锅三组分缩合反应合成1H - 吡唑并[1,2 - a]哒嗪 - 5,8 - 二酮衍生物。测试了一些衍生物对革兰氏阳性和革兰氏阴性细菌的抗菌活性。
首先,成功合成并表征了超顺磁性PAmPDA@FeO纳米复合材料,然后将所得纳米催化剂用于合成吡唑并[1,2 - b]酞嗪和吡唑并[1,2 - a]哒嗪。在无溶剂条件下,于80°C使用0.05 g催化剂,我们获得了所需的1H - 吡唑并[1,2 - b]酞嗪 - 5,10 - 二酮衍生物的最大产率,反应在30分钟内完成。合成了多种产率良好至优异的1H - 吡唑并[1,2 - b]酞嗪 - 5,10 - 二酮衍生物。另一方面,以PAmPDA作为纳米催化剂成功高产率合成了吡唑并[1,2 - a]哒嗪衍生物。根据数据(抑菌圈%),一些衍生物的抗菌活性对金黄色葡萄球菌和大肠杆菌表现出良好的活性。
在本研究中,PAmPDA用于温和地制备1H - 吡唑并[1,2 - a]哒嗪 - 5,8 - 二酮和1H - 吡唑并[1,2 - b]酞嗪 - 5,10 - 二酮衍生物,产率优异且反应时间短。该方法的吸引人之处在于步骤简单、反应更清洁以及使用可回收的纳米催化剂。产品产率令人满意且后处理容易,使其成为此类化合物绿色合成的有用方法。根据数据(抑菌圈%),一些衍生物的抗菌活性对金黄色葡萄球菌和大肠杆菌表现出良好的活性。