• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

4-(2-氯喹啉-3-基)-1-苯基-1H-吡咯-3-羧酸乙酯

Ethyl 4-(2-chloro-quinolin-3-yl)-1-phenyl-1H-pyrrole-3-carboxyl-ate.

作者信息

Benzerka Saida, Bouraiou Abdelmalek, Bouacida Sofiane, Debache Abdelmadjid, Belfaitah Ali

出版信息

Acta Crystallogr Sect E Struct Rep Online. 2008 Oct 15;64(Pt 11):o2115-6. doi: 10.1107/S1600536808032546.

DOI:10.1107/S1600536808032546
PMID:21580979
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2959760/
Abstract

In the mol-ecule of the title compound, C(22)H(17)ClN(2)O(2), the dihedral angles formed by the pyrrole ring with the quinoline and phenyl rings are 67.93 (8) and 28.40 (11)°, respectively. In the crystal structure, mol-ecules are linked into dimers by inter-molecular C-H⋯O hydrogen bonds.

摘要

在标题化合物C₂₂H₁₇ClN₂O₂的分子中,吡咯环与喹啉环和苯环形成的二面角分别为67.93(8)°和28.40(11)°。在晶体结构中,分子通过分子间C—H⋯O氢键连接成二聚体。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dfd4/2959760/7cbb37ceb9ef/e-64-o2115-fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dfd4/2959760/741b664f6ab7/e-64-o2115-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dfd4/2959760/7cbb37ceb9ef/e-64-o2115-fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dfd4/2959760/741b664f6ab7/e-64-o2115-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dfd4/2959760/7cbb37ceb9ef/e-64-o2115-fig2.jpg

相似文献

1
Ethyl 4-(2-chloro-quinolin-3-yl)-1-phenyl-1H-pyrrole-3-carboxyl-ate.4-(2-氯喹啉-3-基)-1-苯基-1H-吡咯-3-羧酸乙酯
Acta Crystallogr Sect E Struct Rep Online. 2008 Oct 15;64(Pt 11):o2115-6. doi: 10.1107/S1600536808032546.
2
Ethyl 4-(4-chloro-anilino)-1-(4-chloro-phen-yl)-2-methyl-5-oxo-2,5-di-hydro-1H-pyrrole-2-carboxyl-ate.4-(4-氯苯胺基)-1-(4-氯苯基)-2-甲基-5-氧代-2,5-二氢-1H-吡咯-2-羧酸乙酯
Acta Crystallogr Sect E Struct Rep Online. 2013 Dec 3;69(Pt 12):o1761-2. doi: 10.1107/S1600536813030560.
3
Ethyl 2-(4-chloro-phen-yl)-1-phenyl-1H-benzimidazole-5-carboxyl-ate.2-(4-氯苯基)-1-苯基-1H-苯并咪唑-5-羧酸乙酯
Acta Crystallogr Sect E Struct Rep Online. 2012 Jun 1;68(Pt 6):o1863. doi: 10.1107/S1600536812022192. Epub 2012 May 23.
4
Ethyl 3,4-dimethyl-5-[(E)-(phenyl-imino)-meth-yl]-1H-pyrrole-2-carboxyl-ate.3,4-二甲基-5-[(E)-(苯基亚氨基)-甲基]-1H-吡咯-2-羧酸乙酯
Acta Crystallogr Sect E Struct Rep Online. 2010 Jun 16;66(Pt 7):o1655. doi: 10.1107/S1600536810022051.
5
Ethyl 3-(4-chloro-phen-yl)-1-(2-oxo-2-phenyl-eth-yl)-1H-pyrazole-5-carboxyl-ate.3-(4-氯苯基)-1-(2-氧代-2-苯基乙基)-1H-吡唑-5-羧酸乙酯
Acta Crystallogr Sect E Struct Rep Online. 2011 Aug 1;67(Pt 8):o1910-1. doi: 10.1107/S1600536811025918. Epub 2011 Jul 6.
6
Ethyl 1-[3-(1H-imidazol-1-yl)prop-yl]-2-(4-chloro-phen-yl)-1H-benzo[d]imidazole-5-carboxyl-ate dihydrate.1-[3-(1H-咪唑-1-基)丙基]-2-(4-氯苯基)-1H-苯并[d]咪唑-5-羧酸乙酯二水合物
Acta Crystallogr Sect E Struct Rep Online. 2011 Sep 1;67(Pt 9):o2405. doi: 10.1107/S1600536811033654. Epub 2011 Aug 27.
7
Ethyl 2-benzyl-3-[3-(4-chloro-phen-yl)-1-phenyl-1H-pyrazol-4-yl]-4,6-dioxo-5-phenyl-octa-hydro-pyrrolo-[3,4-c]pyrrole-1-carboxyl-ate.2-苄基-3-[3-(4-氯苯基)-1-苯基-1H-吡唑-4-基]-4,6-二氧代-5-苯基-八氢-吡咯并[3,4-c]吡咯-1-羧酸乙酯
Acta Crystallogr Sect E Struct Rep Online. 2012 Feb 1;68(Pt 2):o552. doi: 10.1107/S1600536812002450. Epub 2012 Jan 31.
8
Ethyl 1-(4-chloro-phen-yl)-3-[1-(4-meth-oxy-phen-yl)-4-oxo-3-phenyl-azetidin-2-yl]-2-nitro-2,3,10,10a-tetra-hydro-1H,5H-pyr-rolo[1,2-b]isoquinoline-10a-carboxyl-ate.1-(4-氯苯基)-3-[1-(4-甲氧基苯基)-4-氧代-3-苯基氮杂环丁烷-2-基]-2-硝基-2,3,10,10a-四氢-1H,5H-吡咯并[1,2-b]异喹啉-10a-羧酸乙酯
Acta Crystallogr Sect E Struct Rep Online. 2008 Sep 30;64(Pt 10):o2042. doi: 10.1107/S1600536808030961.
9
2-(N-Phenyl-methane-sulfonamido)-ethyl 1H-pyrrole-2-carboxyl-ate.2-(N-苯基-甲磺酰胺基)-乙基 1H-吡咯-2-羧酸酯
Acta Crystallogr Sect E Struct Rep Online. 2011 May 1;67(Pt 5):o1125-6. doi: 10.1107/S160053681101261X. Epub 2011 Apr 13.
10
Ethyl 4-(5-chloro-3-methyl-1-phenyl-1H-pyrazol-4-yl)-6-methyl-2-oxo-1,2,3,4-tetra-hydro-pyrimidine-5-carboxyl-ate.4-(5-氯-3-甲基-1-苯基-1H-吡唑-4-基)-6-甲基-2-氧代-1,2,3,4-四氢嘧啶-5-羧酸乙酯
Acta Crystallogr Sect E Struct Rep Online. 2009 May 7;65(Pt 6):o1229. doi: 10.1107/S1600536809016365.

本文引用的文献

1
A short history of SHELX.SHELX简史。
Acta Crystallogr A. 2008 Jan;64(Pt 1):112-22. doi: 10.1107/S0108767307043930. Epub 2007 Dec 21.
2
Pyrrole synthesis catalyzed by AgOTf or cationic Au(I) complexes.由三氟甲磺酸银(AgOTf)或阳离子金(I)配合物催化的吡咯合成。
J Org Chem. 2006 Jun 9;71(12):4525-9. doi: 10.1021/jo060382c.
3
Synthesis, antimicrobial and antifungal activity of a new class of spiro pyrrolidines.一类新型螺环吡咯烷的合成、抗菌和抗真菌活性
Bioorg Med Chem. 2003 Feb 6;11(3):407-19. doi: 10.1016/s0968-0896(02)00439-x.
4
Synthesis of a novel quinoline derivative, 2-(2-methylquinolin-4-ylamino)-N-phenylacetamide--a potential antileishmanial agent.
Bioorg Med Chem. 2002 Jun;10(6):1687-93. doi: 10.1016/s0968-0896(02)00046-9.
5
Four new bioactive pyrrole-derived alkaloids from the marine sponge Axinella brevistyla.从海洋海绵短柱轴海绵中分离出的四种新的具有生物活性的吡咯衍生生物碱。
J Nat Prod. 2001 Dec;64(12):1576-8. doi: 10.1021/np010280b.
6
Synthesis and evaluation of cryptolepine analogues for their potential as new antimalarial agents.隐丹参酮类似物作为新型抗疟药物潜力的合成与评估
J Med Chem. 2001 Sep 13;44(19):3187-94. doi: 10.1021/jm010929+.