杂环化合物的合成、表征及生物活性研究

Q4 Pharmacology, Toxicology and Pharmaceutics
R. N. Atiya, Zahraa. L. Razzaq, W. I. Yahya, Helen M Neamah
{"title":"杂环化合物的合成、表征及生物活性研究","authors":"R. N. Atiya, Zahraa. L. Razzaq, W. I. Yahya, Helen M Neamah","doi":"10.25258/ijddt.13.1.31","DOIUrl":null,"url":null,"abstract":"Heterocyclic moiety was mentioned to present diverse biological activities such as inhibitors of protein glycation, antibacterial, antifungal, anticancer, antidepressant, anti-inflammatory, antituberculosis, antioxidant, and as antiviral agents, in addition to other biological activities; therefore, many medicines containing heterocyclic moiety have been observed. Due to the pharmacological importance of heterocyclic derivatives, the present work comes as attempt to synthesis of heterocyclic compound involved (tetrazole and pyrazole rings) by series of steps starting from pyrimidin-2-amine, which reacted with 2-chloroacetyl chloride gave compound (1) [2-chloro-N-(pyrimidin-2-yl) acetamide], then the refl ex reaction of the compound (1) with the hydrazine hydrate in ethanol led to compound (2) [2-hydrazinyl-N-(pyrimidin-2-yl)acetamide], the last one reacted with acetyl acetone to form pyrazole ring compound (3) [2-(3,5-dimethyl-1H-pyrazol-1-yl)-N-(pyrimidin-2-yl)acetamide]. In other line another pyrazole derivative was prepared by diazotization of pyrimidin-2-amine with NaNO2/HCl to azo derivative compound (4), which is reacted with acetyl acetone gave compound (5) [3-(2-(pyrimidin-2-yl)hydrazono)pentane-2,4-dione] to react with hydrazine gave pyrazole moiety compound (6) [(2-((1H-pyrazol-4-yl)diazenyl)pyrimidine]. Pyrimidin-2-amine was reacted with 4-hydroxybenzaldehyde in ethanol and glacial acetic acid gave Schiff base compound (7) , which reacted with sodium azide in dioxane to form tetrazole ring compound (8) [4-(1-(pyrimidin-2-yl)-4,5-dihydro-1H-tetrazol-5-yl)phenol]. The spectroscopic techniques were used to confi rmed the chemical structures are FTIR, 1H-NMR. The biological study of pyrazole and tetrazole derivative was evaluated as anti-bacterial against gram-negative (Klebsiella pneumoniae), gram-positive (Enterococcus faecalis) and as anti-fungal against the Candida trichomonas and Candida dubliniensis in concentration 25, 75, 50, and 100 mg/mL. It was found that pyrazole and tetrazole derivative have biological activity against the bacteria and fungi where the tetrazole ring has biological eff ect more than pyrazole ring.","PeriodicalId":13851,"journal":{"name":"International Journal of Drug Delivery Technology","volume":" ","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2023-03-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Synthesis, Characterization and Studying Biological Activity of Heterocyclic Compounds\",\"authors\":\"R. N. Atiya, Zahraa. L. Razzaq, W. I. Yahya, Helen M Neamah\",\"doi\":\"10.25258/ijddt.13.1.31\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Heterocyclic moiety was mentioned to present diverse biological activities such as inhibitors of protein glycation, antibacterial, antifungal, anticancer, antidepressant, anti-inflammatory, antituberculosis, antioxidant, and as antiviral agents, in addition to other biological activities; therefore, many medicines containing heterocyclic moiety have been observed. Due to the pharmacological importance of heterocyclic derivatives, the present work comes as attempt to synthesis of heterocyclic compound involved (tetrazole and pyrazole rings) by series of steps starting from pyrimidin-2-amine, which reacted with 2-chloroacetyl chloride gave compound (1) [2-chloro-N-(pyrimidin-2-yl) acetamide], then the refl ex reaction of the compound (1) with the hydrazine hydrate in ethanol led to compound (2) [2-hydrazinyl-N-(pyrimidin-2-yl)acetamide], the last one reacted with acetyl acetone to form pyrazole ring compound (3) [2-(3,5-dimethyl-1H-pyrazol-1-yl)-N-(pyrimidin-2-yl)acetamide]. In other line another pyrazole derivative was prepared by diazotization of pyrimidin-2-amine with NaNO2/HCl to azo derivative compound (4), which is reacted with acetyl acetone gave compound (5) [3-(2-(pyrimidin-2-yl)hydrazono)pentane-2,4-dione] to react with hydrazine gave pyrazole moiety compound (6) [(2-((1H-pyrazol-4-yl)diazenyl)pyrimidine]. Pyrimidin-2-amine was reacted with 4-hydroxybenzaldehyde in ethanol and glacial acetic acid gave Schiff base compound (7) , which reacted with sodium azide in dioxane to form tetrazole ring compound (8) [4-(1-(pyrimidin-2-yl)-4,5-dihydro-1H-tetrazol-5-yl)phenol]. The spectroscopic techniques were used to confi rmed the chemical structures are FTIR, 1H-NMR. The biological study of pyrazole and tetrazole derivative was evaluated as anti-bacterial against gram-negative (Klebsiella pneumoniae), gram-positive (Enterococcus faecalis) and as anti-fungal against the Candida trichomonas and Candida dubliniensis in concentration 25, 75, 50, and 100 mg/mL. It was found that pyrazole and tetrazole derivative have biological activity against the bacteria and fungi where the tetrazole ring has biological eff ect more than pyrazole ring.\",\"PeriodicalId\":13851,\"journal\":{\"name\":\"International Journal of Drug Delivery Technology\",\"volume\":\" \",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2023-03-25\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"International Journal of Drug Delivery Technology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.25258/ijddt.13.1.31\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"Pharmacology, Toxicology and Pharmaceutics\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"International Journal of Drug Delivery Technology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.25258/ijddt.13.1.31","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"Pharmacology, Toxicology and Pharmaceutics","Score":null,"Total":0}
引用次数: 0

摘要

杂环部分除了具有其他生物活性外,还具有多种生物活性,如蛋白质糖基化抑制剂、抗菌、抗真菌、抗癌、抗抑郁、抗炎、抗结核、抗氧化和抗病毒药物;因此,已经观察到许多含有杂环部分的药物。由于杂环衍生物的药理学重要性,本工作试图通过从嘧啶-2-胺开始的一系列步骤合成涉及的杂环化合物(四唑和吡唑环),嘧啶-2-胺与2-氯乙酰氯反应得到化合物(1)[2-氯-N-(嘧啶-2-基)乙酰胺],然后化合物(1)与肼水合物在乙醇中的回流反应生成化合物(2)[2-肼基-N-(嘧啶-2-基)乙酰胺],最后一个与乙酰丙酮反应生成吡唑环化合物(3)[2-(3,5-二甲基-1H-吡唑-1-基)-N-(吡啶-2-基)丙酰胺]。在另一行中,通过用NaNO2/HCl将嘧啶-2-胺重氮化为偶氮衍生物化合物(4)来制备另一吡唑衍生物,其与乙酰丙酮反应得到化合物(5)[3-(2-(嘧啶-2-基)肼基)戊烷-2,4-二酮]与肼反应得到吡唑部分化合物(6)[(2-(((1H-吡唑-4-基)二氮基)嘧啶]。嘧啶-2-胺与4-羟基苯甲醛在乙醇和冰醋酸中反应得到席夫碱化合物(7),其与叠氮化钠在二恶烷中反应形成四唑环化合物(8)[4-(1-(嘧啶-2-基)-4,5-二氢-1H-四唑-5-基)苯酚]。利用红外光谱、核磁共振氢谱等技术对其化学结构进行了确证。吡唑和四唑衍生物的生物学研究被评估为对浓度为25、75、50和100 mg/mL的革兰氏阴性菌(肺炎克雷伯菌)、革兰氏阳性菌(粪肠球菌)具有抗菌作用,对毛念珠菌和杜氏念珠菌具有抗真菌作用。发现吡唑及其衍生物对细菌和真菌具有生物活性,其中四唑环的生物活性大于吡唑环。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Synthesis, Characterization and Studying Biological Activity of Heterocyclic Compounds
Heterocyclic moiety was mentioned to present diverse biological activities such as inhibitors of protein glycation, antibacterial, antifungal, anticancer, antidepressant, anti-inflammatory, antituberculosis, antioxidant, and as antiviral agents, in addition to other biological activities; therefore, many medicines containing heterocyclic moiety have been observed. Due to the pharmacological importance of heterocyclic derivatives, the present work comes as attempt to synthesis of heterocyclic compound involved (tetrazole and pyrazole rings) by series of steps starting from pyrimidin-2-amine, which reacted with 2-chloroacetyl chloride gave compound (1) [2-chloro-N-(pyrimidin-2-yl) acetamide], then the refl ex reaction of the compound (1) with the hydrazine hydrate in ethanol led to compound (2) [2-hydrazinyl-N-(pyrimidin-2-yl)acetamide], the last one reacted with acetyl acetone to form pyrazole ring compound (3) [2-(3,5-dimethyl-1H-pyrazol-1-yl)-N-(pyrimidin-2-yl)acetamide]. In other line another pyrazole derivative was prepared by diazotization of pyrimidin-2-amine with NaNO2/HCl to azo derivative compound (4), which is reacted with acetyl acetone gave compound (5) [3-(2-(pyrimidin-2-yl)hydrazono)pentane-2,4-dione] to react with hydrazine gave pyrazole moiety compound (6) [(2-((1H-pyrazol-4-yl)diazenyl)pyrimidine]. Pyrimidin-2-amine was reacted with 4-hydroxybenzaldehyde in ethanol and glacial acetic acid gave Schiff base compound (7) , which reacted with sodium azide in dioxane to form tetrazole ring compound (8) [4-(1-(pyrimidin-2-yl)-4,5-dihydro-1H-tetrazol-5-yl)phenol]. The spectroscopic techniques were used to confi rmed the chemical structures are FTIR, 1H-NMR. The biological study of pyrazole and tetrazole derivative was evaluated as anti-bacterial against gram-negative (Klebsiella pneumoniae), gram-positive (Enterococcus faecalis) and as anti-fungal against the Candida trichomonas and Candida dubliniensis in concentration 25, 75, 50, and 100 mg/mL. It was found that pyrazole and tetrazole derivative have biological activity against the bacteria and fungi where the tetrazole ring has biological eff ect more than pyrazole ring.
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
International Journal of Drug Delivery Technology
International Journal of Drug Delivery Technology Pharmacology, Toxicology and Pharmaceutics-Pharmaceutical Science
CiteScore
0.70
自引率
0.00%
发文量
0
期刊介绍: International Journal of Drug Delivery Technology (IJDDT) provides the forum for reporting innovations, production methods, technologies, initiatives and the application of scientific knowledge to the aspects of pharmaceutics, including controlled drug release systems, drug targeting etc. in the form of expert forums, reviews, full research papers, and short communications.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信