• 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

3-氯-6-[4-(2-吡啶基)哌嗪-1-基]哒嗪

3-Chloro-6-[4-(2-pyrid-yl)piperazin-1-yl]pyridazine.

作者信息

Arslan Hakan, Utku Semra, Hardcastle Kenneth I, Gökçe Mehtap, Lense Sheri

出版信息

Acta Crystallogr Sect E Struct Rep Online. 2009 Dec 4;66(Pt 1):o35. doi: 10.1107/S1600536809050727.

DOI:10.1107/S1600536809050727
PMID:21580140
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2980189/
Abstract

In the title compound, C(13)H(14)ClN(5), the piperazine ring adopts a chair conformation and the dihedral angle between the aromatic rings is 13.91 (7)°. The crystal structure is stabilized by weak inter-molecular C-H⋯N hydrogen-bond inter-actions.

摘要

在标题化合物C₁₃H₁₄ClN₅中,哌嗪环呈椅式构象,芳环之间的二面角为13.91 (7)°。晶体结构通过弱分子间C—H⋯N氢键相互作用得以稳定。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9da8/2980189/7c403c96d48b/e-66-00o35-fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9da8/2980189/4d144ec63d94/e-66-00o35-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9da8/2980189/88c3dc8591f7/e-66-00o35-fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9da8/2980189/7c403c96d48b/e-66-00o35-fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9da8/2980189/4d144ec63d94/e-66-00o35-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9da8/2980189/88c3dc8591f7/e-66-00o35-fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9da8/2980189/7c403c96d48b/e-66-00o35-fig3.jpg

相似文献

1
3-Chloro-6-[4-(2-pyrid-yl)piperazin-1-yl]pyridazine.3-氯-6-[4-(2-吡啶基)哌嗪-1-基]哒嗪
Acta Crystallogr Sect E Struct Rep Online. 2009 Dec 4;66(Pt 1):o35. doi: 10.1107/S1600536809050727.
2
3-Chloro-6-{4-[3-(trifluoro-meth-yl)phen-yl]piperazin-1-yl}pyridazine.3-氯-6-{4-[3-(三氟甲基)苯基]哌嗪-1-基}哒嗪
Acta Crystallogr Sect E Struct Rep Online. 2010 Feb 6;66(Pt 3):o532. doi: 10.1107/S1600536810004137.
3
3-Chloro-6-{4-[3-(4-chloro-phen-oxy)prop-yl]piperazin-1-yl}pyridazine.3-氯-6-{4-[3-(4-氯苯氧基)丙基]哌嗪-1-基}哒嗪
Acta Crystallogr Sect E Struct Rep Online. 2010 Feb 27;66(Pt 3):o716. doi: 10.1107/S1600536810005337.
4
1-[4-(4-Chloro-phen-yl)piperazin-1-yl]-3-(6-oxo-3,4-diphenyl-1,6-dihydro-pyridazin-1-yl)propan-1-one.1-[4-(4-氯苯基)哌嗪-1-基]-3-(6-氧代-3,4-二苯基-1,6-二氢哒嗪-1-基)丙-1-酮
Acta Crystallogr Sect E Struct Rep Online. 2012 Sep 1;68(Pt 9):o2720. doi: 10.1107/S160053681203543X. Epub 2012 Aug 15.
5
N-{2-[4-(2-Meth-oxy-phen-yl)piperazin-1-yl]eth-yl}pyridin-2-amine monohydrate.N-{2-[4-(2-甲氧基苯基)哌嗪-1-基]乙基}吡啶-2-胺一水合物
Acta Crystallogr Sect E Struct Rep Online. 2010 Jun 23;66(Pt 7):o1727. doi: 10.1107/S1600536810022816.
6
(1S,2R,3R,6R,7S,8R,10S,11S)-13-{[4-(4-Chloro-phen-yl)piperazin-1-yl]meth-yl}-10-hy-droxy-4,9-dimethyl-3,8,15-trioxatetra-cyclo-[10.3.0.0(2,4).0(7,9)]penta-decan-14-one.(1S,2R,3R,6R,7S,8R,10S,11S)-13-{[4-(4-氯苯基)哌嗪-1-基]甲基}-10-羟基-4,9-二甲基-3,8,15-三氧杂四环-[10.3.0.0(2,4).0(7,9)]十五烷-14-酮
Acta Crystallogr Sect E Struct Rep Online. 2012 Apr 1;68(Pt 4):o1147-8. doi: 10.1107/S1600536812011816. Epub 2012 Mar 24.
7
9α-Hy-droxy-12-{[4-(4-meth-oxy-phen-yl)piperazin-1-yl]meth-yl}-4,8-dimethyl-3,14-dioxatricyclo-[9.3.0.0]tetra-dec-7-en-13-one.9α-羟基-12-{[4-(4-甲氧基苯基)哌嗪-1-基]甲基}-4,8-二甲基-3,14-二氧杂三环-[9.3.0.0]十四碳-7-烯-13-酮
Acta Crystallogr Sect E Struct Rep Online. 2012 Mar 1;68(Pt 3):o589-90. doi: 10.1107/S1600536812003662. Epub 2012 Feb 4.
8
5-Meth-oxy-2-{[4-(morpholin-4-yl)phen-yl]imino-meth-yl}phenol.5-甲氧基-2-{[4-(吗啉-4-基)苯基]亚氨基甲基}苯酚
Acta Crystallogr Sect E Struct Rep Online. 2011 Sep 1;67(Pt 9):o2501. doi: 10.1107/S1600536811034659. Epub 2011 Aug 27.
9
2-[4-(2-Meth-oxy-phen-yl)piperazin-1-yl]-N-(pyridin-2-yl)acetamide.2-[4-(2-甲氧基苯基)哌嗪-1-基]-N-(吡啶-2-基)乙酰胺
Acta Crystallogr Sect E Struct Rep Online. 2010 Dec 24;67(Pt 1):o223. doi: 10.1107/S1600536810053067.
10
(3R*,4R*)-1-(4-Chloro-phen-yl)-4-[2-hy-droxy-3-(morpholinomethyl)-phen-yl]-3-phen-oxy-azetidin-2-one.(3R*,4R*)-1-(4-氯苯基)-4-[2-羟基-3-(吗啉甲基)苯基]-3-苯氧基氮杂环丁烷-2-酮
Acta Crystallogr Sect E Struct Rep Online. 2011 Jan 12;67(Pt 2):o325. doi: 10.1107/S1600536811000675.

引用本文的文献

1
3-Chloro-6-{4-[3-(trifluoro-meth-yl)phen-yl]piperazin-1-yl}pyridazine.3-氯-6-{4-[3-(三氟甲基)苯基]哌嗪-1-基}哒嗪
Acta Crystallogr Sect E Struct Rep Online. 2010 Feb 6;66(Pt 3):o532. doi: 10.1107/S1600536810004137.

本文引用的文献

1
Synthesis and analgesic and anti-inflammatory activities 6-substituted-3(2H)-pyridazinone-2-acetyl-2-(p-substituted/nonsubstituted benzal)hydrazone derivatives.6-取代-3(2H)-哒嗪酮-2-乙酰基-2-(对-取代/未取代苯亚甲基)腙衍生物的合成及其镇痛和抗炎活性
Eur J Med Chem. 2009 Sep;44(9):3760-4. doi: 10.1016/j.ejmech.2009.04.048. Epub 2009 May 9.
2
Synthesis and analgesic and anti-inflammatory activity of ethyl (6-substituted-3 (2H)-pyridazinone-2-yl)acetate derivatives.(6-取代-3(2H)-哒嗪酮-2-基)乙酸乙酯衍生物的合成及其镇痛和抗炎活性
Arzneimittelforschung. 2007;57(12):777-81. doi: 10.1055/s-0031-1296679.
3
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.
4
Synthesis of new Mannich bases of arylpyridazinones as analgesic and anti-inflammatory agents.作为镇痛和抗炎剂的芳基哒嗪酮新曼尼希碱的合成。
Arzneimittelforschung. 2005;55(6):318-25. doi: 10.1055/s-0031-1296866.
5
Synthesis and evaluation of the analgesic and anti-inflammatory activity of new 3(2H)-pyridazinone derivatives.新型3(2H)-哒嗪酮衍生物的镇痛及抗炎活性的合成与评价
Arzneimittelforschung. 2004;54(7):396-401. doi: 10.1055/s-0031-1296990.
6
Synthesis and analgesic and antiinflammatory activity of methyl 6-substituted-3(2h)-pyridazinone-2-ylacetate derivatives.6-取代-3(2H)-哒嗪酮-2-基乙酸甲酯衍生物的合成及其镇痛和抗炎活性
Arch Pharm (Weinheim). 2004 Aug;337(8):445-52. doi: 10.1002/ardp.200400896.
7
Amide derivatives of [6-(5-methyl-3-phenylpyrazole-1-yl)-3(2H)-pyridazinone-2-yl]acetic acids as potential analgesic and anti-inflammatory compounds.[6-(5-甲基-3-苯基吡唑-1-基)-3(2H)-哒嗪酮-2-基]乙酸的酰胺衍生物作为潜在的镇痛和抗炎化合物。
Arch Pharm (Weinheim). 2004 Jan;337(1):7-14. doi: 10.1002/ardp.200200738.
8
SYNTHESIS AND PHARMACOLOGICAL STUDY OF NEW PIPERAZINE DERIVATIVES. I. BENZYLPIPERAZINES.新型哌嗪衍生物的合成与药理研究。I. 苄基哌嗪
J Med Chem. 1963 Sep;6:541-4. doi: 10.1021/jm00341a016.
9
[(3-Chlorophenyl)piperazinylpropyl]pyridazinones and analogues as potent antinociceptive agents.[(3-氯苯基)哌嗪基丙基]哒嗪酮及其类似物作为强效抗伤害感受剂
J Med Chem. 2003 Mar 13;46(6):1055-9. doi: 10.1021/jm021057u.
10
Synthesis and antinociceptive activity of 6-substituted-3-pyridazinone derivatives.
Farmaco. 2001 Mar;56(3):233-7. doi: 10.1016/s0014-827x(01)01037-0.