• 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

格罗布克-布莱克本-比内梅反应

The Groebke-Blackburn-Bienaymé Reaction.

作者信息

Boltjes André, Dömling Alexander

机构信息

Department of Drug Design, Groningen Research Institute of Pharmacy, University of Groningen, A. Deusinglaan 1, Groningen, The Netherlands.

出版信息

Eur J Chem. 2019 Nov 14;2019(42):7007-7049. doi: 10.1002/ejoc.201901124. Epub 2019 Aug 30.

DOI:10.1002/ejoc.201901124
PMID:34012704
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8130801/
Abstract

Imidazo[1,2-]pyridine is a well-known scaffold in many marketed drugs, such as Zolpidem, Minodronic acid, Miroprofen and DS-1 and it also serves as a broadly applied pharmacophore in drug discovery. The scaffold revoked a wave of interest when Groebke, Blackburn and Bienaymé reported independently a new three component reaction resulting in compounds with the imidazo[1,2-]-heterocycles as a core structure. During the course of two decades the Groebke Blackburn Bienaymé (GBB-3CR) reaction has emerged as a very important multicomponent reaction (MCR), resulting in over a hundred patents and a great number of publications in various fields of interest. Now two compounds derived from GBB-3CR chemistry received FDA approval. To celebrate the first 20 years of GBB-chemistry, we present an overview of the chemistry of the GBB-3CR, including an analysis of each of the three starting material classes, solvents and catalysts. Additionally, a list of patents and their applications and a more in-depth summary of the biological targets that were addressed, including structural biology analysis, is given.

摘要

咪唑并[1,2 - ]吡啶是许多已上市药物中熟知的骨架结构,如唑吡坦、米诺膦酸、米洛芬和DS - 1,它在药物研发中也是一种广泛应用的药效基团。当格罗布克、布莱克本和比奈梅各自独立报道一种新的三组分反应,该反应生成以咪唑并[1,2 - ]杂环为核心结构的化合物时,这种骨架结构引起了广泛关注。在二十年的时间里,格罗布克 - 布莱克本 - 比奈梅(GBB - 3CR)反应已成为一种非常重要 的多组分反应(MCR),产生了一百多项专利以及众多在各个感兴趣领域的出版物。现在,两种源自GBB - 3CR化学的化合物已获得美国食品药品监督管理局(FDA)批准。为庆祝GBB化学的首个二十年,我们概述了GBB - 3CR的化学,包括对三类起始原料、溶剂和催化剂的分析。此外,还列出了专利及其应用,并对所涉及的生物学靶点进行了更深入的总结,包括结构生物学分析。

相似文献

1
The Groebke-Blackburn-Bienaymé Reaction.格罗布克-布莱克本-比内梅反应
Eur J Chem. 2019 Nov 14;2019(42):7007-7049. doi: 10.1002/ejoc.201901124. Epub 2019 Aug 30.
2
Diversity-Oriented Synthesis of [2.2]Paracyclophane-derived Fused Imidazo[1,2-a]heterocycles by Groebke-Blackburn-Bienaymé Reaction: Accessing Cyclophanyl Imidazole Ligands Library.导向多样性的[2.2]并环芳烷衍生稠合咪唑并[1,2-a]杂环的 Groebke-Blackburn-Bienaymé 反应合成:环芳基咪唑配体库的构建。
Chemistry. 2022 Jan 13;28(3):e202103511. doi: 10.1002/chem.202103511. Epub 2021 Dec 8.
3
The Groebke-Blackburn-Bienaymé reaction in its maturity: innovation and improvements since its 21st birthday (2019-2023).格罗布克-布莱克本-比内梅反应步入成熟:自其21岁生日(2019 - 2023年)以来的创新与改进
Beilstein J Org Chem. 2024 Aug 1;20:1839-1879. doi: 10.3762/bjoc.20.162. eCollection 2024.
4
Trends in the Synthesis of Antimicrobial Derivatives by using the Gewald, Strecker, and Groebke-Blackburn-Bienaymé (GBB) Reactions.利用格沃尔德(Gewald)、斯特雷克(Strecker)和格罗贝克尔-布莱克本-拜恩梅(Groebke-Blackburn-Bienaymé,GBB)反应合成抗菌衍生物的趋势。
Med Chem. 2024;20(7):663-688. doi: 10.2174/0115734064282699240315042428.
5
Synthesis of Imidazo[1,2-]pyridine-Fused 1,3-Benzodiazepine Derivatives with Anticancer Activity via a One-Pot Cascade GBB-3CR/Pd(II)-Catalyzed Azide-Isocyanide Coupling/Cyclization Process.通过一锅法级联GBB-3CR/Pd(II)催化的叠氮化物-异腈偶联/环化过程合成具有抗癌活性的咪唑并[1,2-]吡啶稠合的1,3-苯并二氮杂卓衍生物。
J Org Chem. 2023 Sep 15;88(18):13125-13134. doi: 10.1021/acs.joc.3c01341. Epub 2023 Aug 24.
6
Efficient synthesis of glycosylated imidazo[1,2-a]pyridines via solvent catalysed Groebke-Blackburn-Bienayme reaction.通过溶剂催化 Groebke-Blackburn-Bienayme 反应高效合成糖基化咪唑并[1,2-a]吡啶。
Carbohydr Res. 2023 Dec;534:108974. doi: 10.1016/j.carres.2023.108974. Epub 2023 Oct 23.
7
Synthesis of imidazo[1,2-]pyridine-containing peptidomimetics by tandem of Groebke-Blackburn-Bienaymé and Ugi reactions.通过格罗布克-布莱克本-比纳梅反应和乌吉反应串联合成含咪唑并[1,2 - ]吡啶的拟肽
Beilstein J Org Chem. 2023 May 26;19:727-735. doi: 10.3762/bjoc.19.53. eCollection 2023.
8
HPW-Catalyzed environmentally benign approach to imidazo[1,2-]pyridines.基于HPW催化的咪唑并[1,2 - ]吡啶的环境友好型合成方法。
Beilstein J Org Chem. 2024 Mar 19;20:628-637. doi: 10.3762/bjoc.20.55. eCollection 2024.
9
Novel 5-Nitrofuran-Tagged Imidazo-Fused Azines and Azoles Amenable by the Groebke-Blackburn-Bienaymé Multicomponent Reaction: Activity Profile against ESKAPE Pathogens and Mycobacteria.新型5-硝基呋喃标记的咪唑稠合嗪类和唑类化合物,可通过格罗布克-布莱克本-比奈梅多组分反应合成:对ESKAPE病原体和分枝杆菌的活性谱
Biomedicines. 2022 Sep 6;10(9):2203. doi: 10.3390/biomedicines10092203.
10
A practical and efficient approach to imidazo[1,2-]pyridine-fused isoquinolines through the post-GBB transformation strategy.一种通过后GBB转化策略合成咪唑并[1,2 - ]吡啶稠合异喹啉的实用且高效的方法。
Beilstein J Org Chem. 2017 May 4;13:817-824. doi: 10.3762/bjoc.13.82. eCollection 2017.

引用本文的文献

1
Scaffold-hopping for molecular glues targeting the 14-3-3/ERα complex.针对14-3-3/雌激素受体α复合物的分子胶的支架跳跃
Nat Commun. 2025 Jul 14;16(1):6467. doi: 10.1038/s41467-025-61176-4.
2
A multicomponent reaction-initiated synthesis of imidazopyridine-fused isoquinolinones.一种基于多组分反应引发的咪唑并吡啶稠合异喹啉酮的合成方法。
Beilstein J Org Chem. 2025 Jun 13;21:1161-1169. doi: 10.3762/bjoc.21.92. eCollection 2025.
3
The Evolution of Fluorescein into A Potential Theranostic Tool.荧光素向潜在诊疗工具的演变。

本文引用的文献

1
An efficient and environmentally sustainable domino protocol for the synthesis of structurally diverse spiroannulated pyrimidophenazines using erbium doped TiO nanoparticles as a recyclable and reusable heterogeneous acid catalyst.一种高效且环境可持续的多米诺骨牌反应方案,用于使用掺铒的TiO纳米颗粒作为可循环利用的多相酸催化剂合成结构多样的螺环嘧啶并菲嗪。
RSC Adv. 2018 Aug 28;8(53):30430-30440. doi: 10.1039/c8ra04919j. eCollection 2018 Aug 24.
2
Multiple Multicomponent Reactions: Unexplored Substrates, Selective Processes, and Versatile Chemotypes in Biomedicine.多组分反应:在生物医学中探索未知的底物、选择性过程和多功能化学型。
Chemistry. 2018 Sep 25;24(54):14513-14521. doi: 10.1002/chem.201802877. Epub 2018 Aug 28.
3
Chemistry. 2025 Jun 17;31(34):e202501513. doi: 10.1002/chem.202501513. Epub 2025 May 13.
4
Formaldehyde surrogates in multicomponent reactions.多组分反应中的甲醛替代物
Beilstein J Org Chem. 2025 Mar 13;21:564-595. doi: 10.3762/bjoc.21.45. eCollection 2025.
5
Synthesis and biological activities of 3-aminoimidazo[1,2-α]pyridine compounds.3-氨基咪唑并[1,2-α]吡啶化合物的合成及生物活性
BMC Chem. 2025 Feb 22;19(1):48. doi: 10.1186/s13065-025-01412-6.
6
Navigating Unexplored Territories of the Interrupted Ugi and Passerini Reactions toward Peptidomimetics.探索乌吉反应和帕塞里尼反应在肽模拟物合成中的未知领域。
Org Lett. 2025 Feb 28;27(8):1829-1834. doi: 10.1021/acs.orglett.4c04810. Epub 2025 Feb 17.
7
Phytotoxicity Study of (Amino)imidazo[1,2-]pyridine Derivatives Toward the Control of , , and Weeds.(氨基)咪唑并[1,2 - ]吡啶衍生物对防治苋属植物、藜属植物和稗草的植物毒性研究
J Agric Food Chem. 2025 Jan 8;73(1):298-317. doi: 10.1021/acs.jafc.4c09477. Epub 2024 Dec 28.
8
Atroposelective synthesis of axially chiral imidazo[1,2-]pyridines via asymmetric multicomponent reaction.通过不对称多组分反应实现轴手性咪唑并[1,2 - ]吡啶的对映选择性合成。
Sci Adv. 2024 Dec 6;10(49):eadr6135. doi: 10.1126/sciadv.adr6135. Epub 2024 Dec 4.
9
Crafting Molecular Tools for 15-Lipoxygenase-1 in a Single Step.一步法构建15-脂氧合酶-1的分子工具
Angew Chem Int Ed Engl. 2025 Feb 3;64(6):e202418291. doi: 10.1002/anie.202418291. Epub 2024 Nov 22.
10
Identification of a New Promising BAG3 Modulator Featuring the Imidazopyridine Scaffold.鉴定一种新型有前途的 BAG3 调节剂,其特征为咪唑并吡啶骨架。
Molecules. 2024 Oct 25;29(21):5051. doi: 10.3390/molecules29215051.
A New Heterocyclic Multicomponent Reaction For the Combinatorial Synthesis of Fused 3-Aminoimidazoles.
一种用于组合合成稠合 3-氨基咪唑的新型杂环多组分反应。
Angew Chem Int Ed Engl. 1998 Sep 4;37(16):2234-2237. doi: 10.1002/(SICI)1521-3773(19980904)37:16<2234::AID-ANIE2234>3.0.CO;2-R.
4
Multicomponent reactions provide key molecules for secret communication.多组分反应为秘密通讯提供关键分子。
Nat Commun. 2018 Apr 12;9(1):1439. doi: 10.1038/s41467-018-03784-x.
5
D3R Grand Challenge 2: blind prediction of protein-ligand poses, affinity rankings, and relative binding free energies.D3R 大挑战 2:蛋白质-配体构象、亲和力排序和相对结合自由能的盲预测。
J Comput Aided Mol Des. 2018 Jan;32(1):1-20. doi: 10.1007/s10822-017-0088-4. Epub 2017 Dec 4.
6
Scaffold hopping via ANCHOR.QUERY: β-lactams as potent p53-MDM2 antagonists.通过ANCHOR.QUERY进行骨架跳跃:β-内酰胺作为有效的p53-MDM2拮抗剂。
Medchemcomm. 2017 May 1;8(5):1046-1052. doi: 10.1039/C7MD00058H. Epub 2017 Mar 15.
7
AnchorQuery: Rapid online virtual screening for small-molecule protein-protein interaction inhibitors.锚定查询:用于小分子蛋白质-蛋白质相互作用抑制剂的快速在线虚拟筛选
Protein Sci. 2018 Jan;27(1):229-232. doi: 10.1002/pro.3303. Epub 2017 Oct 24.
8
Nonacidic Farnesoid X Receptor Modulators.非酸性法尼醇X受体调节剂
J Med Chem. 2017 Aug 24;60(16):7199-7205. doi: 10.1021/acs.jmedchem.7b00903. Epub 2017 Aug 8.
9
Discovery, Structure-Activity Relationship, and Binding Mode of an Imidazo[1,2-a]pyridine Series of Autotaxin Inhibitors.咪唑并[1,2 - a]吡啶类自分泌运动因子抑制剂的发现、构效关系及结合模式
J Med Chem. 2017 Sep 14;60(17):7371-7392. doi: 10.1021/acs.jmedchem.7b00647. Epub 2017 Aug 18.
10
Discovery of imidazopyridines containing isoindoline-1,3-dione framework as a new class of BACE1 inhibitors: Design, synthesis and SAR analysis.发现含异吲哚啉-1,3-二酮骨架的咪唑并吡啶类化合物作为新型β-分泌酶1(BACE1)抑制剂:设计、合成及构效关系分析
Eur J Med Chem. 2017 Sep 29;138:729-737. doi: 10.1016/j.ejmech.2017.06.040. Epub 2017 Jun 24.