新型二茂铁-吡唑啉[1,5- A]嘧啶杂合体:一种易于环境友好的区域选择性合成、结构解析及其抗氧化、抗菌和抗生物膜活性

IF 1.7 4区 化学 Q3 Chemistry Journal of Chemical Sciences Pub Date : 2022-07-20 DOI:10.1007/s12039-022-02064-y
SUSMA DAS, SHIVANGI BORKOTOKY, MAXMILLANDO RYMBAI, VEDANT V BORAH, JAYANTI D ROY, SHUNAN KAPING, PHILIPPE HELISSEY, JAI N VISHWAKARMA
{"title":"新型二茂铁-吡唑啉[1,5- A]嘧啶杂合体:一种易于环境友好的区域选择性合成、结构解析及其抗氧化、抗菌和抗生物膜活性","authors":"SUSMA DAS,&nbsp;SHIVANGI BORKOTOKY,&nbsp;MAXMILLANDO RYMBAI,&nbsp;VEDANT V BORAH,&nbsp;JAYANTI D ROY,&nbsp;SHUNAN KAPING,&nbsp;PHILIPPE HELISSEY,&nbsp;JAI N VISHWAKARMA","doi":"10.1007/s12039-022-02064-y","DOIUrl":null,"url":null,"abstract":"<div><p>It was observed that when two prominent bioactive compounds fused together, the new hybrid showed much more promising possessions. Aiming this, here we have fused pyrazolo[1,5-<i>a</i>]pyrimidines with ferrocene, both of which are popularly known as the bio-active molecular core, employing a very simple and facile synthetic strategy using a mild acid KHSO<sub>4</sub> as a catalyst under ultrasonic irradiation. The structures of these synthesized novel compounds were confirmed by their spectral and analytical data. The single-crystal X-ray crystallographic analysis of a selected compound reveals that the 7-ferrocenyl-pyrazolo[1,5-<i>a</i>]pyrimidine (C<sub>22</sub>H<sub>16</sub>ClFeN<sub>3</sub>) hybrid interestingly exists as a dimer and forms a triclinic crystal system with P<sub>1</sub> space group (no. 2), a = 7.554(3) Å, b = 13.650(6) Å, c = 18.444(8) Å, α = 96.938(7)<sup>o</sup>, β = 90.034(7)<sup>o</sup>, γ = 106.015(6)<sup>o</sup>, V = 1813.5(14) Å<sup>3</sup>, Z = 4, µ(Mo<i>K</i>α)= 0.990 mm<sup>−1</sup>, wavelength = 0.71073 Å, D<sub>calc</sub> = 1.515 g/cm<sup>3</sup> with 42808 measured reflection (4.452° ≤ 2θ ≤ 58.312°), 9524 unique reflections (R<sub>int</sub> = 0.1267, R<sub>sigma</sub> = 0.1390) were used in all the calculations. The final R<sub>1</sub> obtained was 0.0570 (I&gt;2σ(<i>I</i>)) with wR<sub>2</sub> = 0.1656 for all data. Most of the compounds exhibited encouraging antioxidant activities like compounds <b>3b-c</b>, <b>3k-l</b> and <b>3n</b> exhibited prominent nitric-oxide scavenging activities, while compounds <b>3a-d</b>, <b>3g</b>, <b>3k</b>, <b>3n</b>, and <b>3o</b> are promising DPPH-scavengers. Compounds <b>3i-k</b> and <b>3m</b> exhibited antibacterial activities at MIC of 500 µg/mL, while <b>3p</b> exhibited activities at MIC of 250 µg/mL. Five of the compounds, <b>3i</b>-<b>k</b>, <b>3m</b>, and <b>3p</b>, were found to possess anti-biofilm activities against both Gram-positive and Gram-negative bacteria.</p><h3>Graphical abstract</h3>\n <div><figure><div><div><picture><source><img></source></picture></div></div></figure></div>\n <p><i>Synopsis</i>: Novel ferrocene-pyrazolo[1,5-a]pyrimidine hybrids were synthesized and investigated for their anti-oxidant, anti-bacterial and anti-biofilm properties. Almost all of the new compounds mentioned have anti-oxidant capabilities and a few of them also exhibited anti-bacterial and anti-biofilm properties </p></div>","PeriodicalId":50242,"journal":{"name":"Journal of Chemical Sciences","volume":"134 3","pages":""},"PeriodicalIF":1.7000,"publicationDate":"2022-07-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"2","resultStr":"{\"title\":\"Novel ferrocene-pyrazolo[1,5-a]pyrimidine hybrids: A facile environment-friendly regioselective synthesis, structure elucidation, and their antioxidant, antibacterial, and anti-biofilm activities\",\"authors\":\"SUSMA DAS,&nbsp;SHIVANGI BORKOTOKY,&nbsp;MAXMILLANDO RYMBAI,&nbsp;VEDANT V BORAH,&nbsp;JAYANTI D ROY,&nbsp;SHUNAN KAPING,&nbsp;PHILIPPE HELISSEY,&nbsp;JAI N VISHWAKARMA\",\"doi\":\"10.1007/s12039-022-02064-y\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>It was observed that when two prominent bioactive compounds fused together, the new hybrid showed much more promising possessions. Aiming this, here we have fused pyrazolo[1,5-<i>a</i>]pyrimidines with ferrocene, both of which are popularly known as the bio-active molecular core, employing a very simple and facile synthetic strategy using a mild acid KHSO<sub>4</sub> as a catalyst under ultrasonic irradiation. The structures of these synthesized novel compounds were confirmed by their spectral and analytical data. The single-crystal X-ray crystallographic analysis of a selected compound reveals that the 7-ferrocenyl-pyrazolo[1,5-<i>a</i>]pyrimidine (C<sub>22</sub>H<sub>16</sub>ClFeN<sub>3</sub>) hybrid interestingly exists as a dimer and forms a triclinic crystal system with P<sub>1</sub> space group (no. 2), a = 7.554(3) Å, b = 13.650(6) Å, c = 18.444(8) Å, α = 96.938(7)<sup>o</sup>, β = 90.034(7)<sup>o</sup>, γ = 106.015(6)<sup>o</sup>, V = 1813.5(14) Å<sup>3</sup>, Z = 4, µ(Mo<i>K</i>α)= 0.990 mm<sup>−1</sup>, wavelength = 0.71073 Å, D<sub>calc</sub> = 1.515 g/cm<sup>3</sup> with 42808 measured reflection (4.452° ≤ 2θ ≤ 58.312°), 9524 unique reflections (R<sub>int</sub> = 0.1267, R<sub>sigma</sub> = 0.1390) were used in all the calculations. The final R<sub>1</sub> obtained was 0.0570 (I&gt;2σ(<i>I</i>)) with wR<sub>2</sub> = 0.1656 for all data. Most of the compounds exhibited encouraging antioxidant activities like compounds <b>3b-c</b>, <b>3k-l</b> and <b>3n</b> exhibited prominent nitric-oxide scavenging activities, while compounds <b>3a-d</b>, <b>3g</b>, <b>3k</b>, <b>3n</b>, and <b>3o</b> are promising DPPH-scavengers. Compounds <b>3i-k</b> and <b>3m</b> exhibited antibacterial activities at MIC of 500 µg/mL, while <b>3p</b> exhibited activities at MIC of 250 µg/mL. Five of the compounds, <b>3i</b>-<b>k</b>, <b>3m</b>, and <b>3p</b>, were found to possess anti-biofilm activities against both Gram-positive and Gram-negative bacteria.</p><h3>Graphical abstract</h3>\\n <div><figure><div><div><picture><source><img></source></picture></div></div></figure></div>\\n <p><i>Synopsis</i>: Novel ferrocene-pyrazolo[1,5-a]pyrimidine hybrids were synthesized and investigated for their anti-oxidant, anti-bacterial and anti-biofilm properties. Almost all of the new compounds mentioned have anti-oxidant capabilities and a few of them also exhibited anti-bacterial and anti-biofilm properties </p></div>\",\"PeriodicalId\":50242,\"journal\":{\"name\":\"Journal of Chemical Sciences\",\"volume\":\"134 3\",\"pages\":\"\"},\"PeriodicalIF\":1.7000,\"publicationDate\":\"2022-07-20\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"2\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Chemical Sciences\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://link.springer.com/article/10.1007/s12039-022-02064-y\",\"RegionNum\":4,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"Chemistry\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Chemical Sciences","FirstCategoryId":"92","ListUrlMain":"https://link.springer.com/article/10.1007/s12039-022-02064-y","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"Chemistry","Score":null,"Total":0}
引用次数: 2

摘要

人们观察到,当两种突出的生物活性化合物融合在一起时,新的杂交种显示出更有希望的特性。针对这一点,我们将吡唑[1,5-a]嘧啶与二茂铁融合,这两种物质通常被称为生物活性分子核心,采用一种非常简单和容易的合成策略,使用温和的硫酸氢钾作为催化剂,在超声波照射下。这些合成的新化合物的结构经光谱和分析数据证实。单晶x射线晶体学分析表明,7-二茂铁基-吡唑[1,5-a]嘧啶(C22H16ClFeN3)杂化物有趣地以二聚体的形式存在,并与P1空间群形成三斜晶体体系。2), a = 7.554(3) Å, b = 13.650(6) Å, c = 18.444(8) Å, α = 96.938(7)o, β = 90.034(7)o, γ = 106.015(6)o, V = 1813.5(14) Å3, Z = 4,µ(MoKα)= 0.990 mm−1,波长= 0.71073 Å, Dcalc = 1.515 g/cm3,测量反射42808个(4.452°≤2θ≤58.312°),唯一反射9524个(Rint = 0.1267, Rsigma = 0.1390)。最终得到的R1为0.0570 (I>2σ(I)), wR2 = 0.1656。化合物3b-c、3k- 1和3n具有较强的抗氧化活性,而化合物3a-d、3g、3k、3n和30是较有前景的dpph清除剂。化合物3i-k和3m在MIC为500µg/mL时表现出抗菌活性,而3p在MIC为250µg/mL时表现出抗菌活性。其中5个化合物,3i-k, 3m和3p,被发现对革兰氏阳性和革兰氏阴性细菌都具有抗生物膜活性。摘要:合成了新型二茂铁-吡唑啉[1,5-a]嘧啶杂合体,并对其抗氧化、抗菌和抗生物膜性能进行了研究。几乎所有的新化合物都具有抗氧化能力,其中一些化合物还具有抗菌和抗生物膜的特性
本文章由计算机程序翻译,如有差异,请以英文原文为准。

摘要图片

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
Novel ferrocene-pyrazolo[1,5-a]pyrimidine hybrids: A facile environment-friendly regioselective synthesis, structure elucidation, and their antioxidant, antibacterial, and anti-biofilm activities

It was observed that when two prominent bioactive compounds fused together, the new hybrid showed much more promising possessions. Aiming this, here we have fused pyrazolo[1,5-a]pyrimidines with ferrocene, both of which are popularly known as the bio-active molecular core, employing a very simple and facile synthetic strategy using a mild acid KHSO4 as a catalyst under ultrasonic irradiation. The structures of these synthesized novel compounds were confirmed by their spectral and analytical data. The single-crystal X-ray crystallographic analysis of a selected compound reveals that the 7-ferrocenyl-pyrazolo[1,5-a]pyrimidine (C22H16ClFeN3) hybrid interestingly exists as a dimer and forms a triclinic crystal system with P1 space group (no. 2), a = 7.554(3) Å, b = 13.650(6) Å, c = 18.444(8) Å, α = 96.938(7)o, β = 90.034(7)o, γ = 106.015(6)o, V = 1813.5(14) Å3, Z = 4, µ(MoKα)= 0.990 mm−1, wavelength = 0.71073 Å, Dcalc = 1.515 g/cm3 with 42808 measured reflection (4.452° ≤ 2θ ≤ 58.312°), 9524 unique reflections (Rint = 0.1267, Rsigma = 0.1390) were used in all the calculations. The final R1 obtained was 0.0570 (I>2σ(I)) with wR2 = 0.1656 for all data. Most of the compounds exhibited encouraging antioxidant activities like compounds 3b-c, 3k-l and 3n exhibited prominent nitric-oxide scavenging activities, while compounds 3a-d, 3g, 3k, 3n, and 3o are promising DPPH-scavengers. Compounds 3i-k and 3m exhibited antibacterial activities at MIC of 500 µg/mL, while 3p exhibited activities at MIC of 250 µg/mL. Five of the compounds, 3i-k, 3m, and 3p, were found to possess anti-biofilm activities against both Gram-positive and Gram-negative bacteria.

Graphical abstract

Synopsis: Novel ferrocene-pyrazolo[1,5-a]pyrimidine hybrids were synthesized and investigated for their anti-oxidant, anti-bacterial and anti-biofilm properties. Almost all of the new compounds mentioned have anti-oxidant capabilities and a few of them also exhibited anti-bacterial and anti-biofilm properties

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
Journal of Chemical Sciences
Journal of Chemical Sciences Chemistry-General Chemistry
CiteScore
2.90
自引率
5.90%
发文量
107
审稿时长
12 months
期刊介绍: Journal of Chemical Sciences is a monthly journal published by the Indian Academy of Sciences. It formed part of the original Proceedings of the Indian Academy of Sciences – Part A, started by the Nobel Laureate Prof C V Raman in 1934, that was split in 1978 into three separate journals. It was renamed as Journal of Chemical Sciences in 2004. The journal publishes original research articles and rapid communications, covering all areas of chemical sciences. A significant feature of the journal is its special issues, brought out from time to time, devoted to conference symposia/proceedings in frontier areas of the subject, held not only in India but also in other countries.
期刊最新文献
Peripheral (anti)aromaticity in the singlet and triplet states of cyclopenta[fg]acenaphthylene, pyrrolo[2,1,5-cd]indolizine and 2a1 boracyclopenta[cd]indene: NICS scan approach High-resolution rovibrational cavity ring-down spectroscopy of (1200←0200) vibrational band of β-site-specific N2O isotopologue near 7.8 µm region Polythiophene, polypyrrole-NiO ternary hybrid nanocomposites: structural, morphological, dielectric and electrical properties Catalysis via bimetallic Pd-Sn nanoparticles: green oxidation of secondary benzyl alcohol in water in the absence of base Synthesis and Photoelectric Properties of D-A Conjugated Polymers of Benzothiadiazoles with Different Molecular Weights
×
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
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1