CAS: 7223-50-9; N-Propargylphthalimide

该化合物是一种化学化合物,具有异族结构特征,有由苯环和五人组成的含氮环组成的引信环系统.该化合物通常呈现黄色至橙色,并因其在有机合成和药用化学中的潜在用途而闻名.它拥有一种可影响其再活动性和溶性特性的丙烯基替代成分.二人功能组的存在表明它可以参与各种化学反应,例如核核分裂嗜好菌添加物或循环添加物.此外,该化合物可能展示生物活动,使其在药用研究中引起兴趣.其稳定性和再活性可能因条件而不同,例如pH和温度,而且一般会因潜在毒性而得到谨慎处理.与许多有机化合物一样,在实验室环境中与该物质打交道时,应当遵循适当的安全议定书.

结构式图片

欧盟法规

ECHA物质C&L通报REACH预注册

上下游产品

CAS号106-96-7 溴代丙炔 | CAS号1074-82-4 邻苯二甲酰亚胺钾盐 | CAS号624-65-7 3-氯丙炔 | CAS号16156-58-4 甲磺酸-2-丙炔-1-醇 | CAS号107-19-7 丙炔醇 | CAS号119812-51-0 邻苯二甲酰亚胺-DBU盐 | CAS号22509-74-6 N-乙氧羰基邻苯二甲酰亚胺 | CAS号2450-71-7 炔丙胺 | CAS号3416-57-7 邻苯二甲酰亚胺基丙酮 | CAS号19446-30-1 2-[4-(az°Can-1-... | CAS号19446-29-8 2-[4-(azepan-1-... | CAS号2450-71-7 炔丙胺 | CAS号132456-42-9 3-hydroxy-2-pro... | CAS号5428-09-1 N-烯丙基邻苯二甲酰亚胺 | CAS号5323-50-2 N-丙基酞酰亚胺

合成工艺路线路线简述

  • 合成目标产物 N-Propargylphthalimide 主要起始原料 Potassium Phthalimide And Propargyl Bromide
  • (文献来源)合成步骤主要原料 Potassium Phthalimide 和 Propargyl Bromide
在 Pyridinium Chlorochromate体系中,用 二氯甲烷 作为反应溶剂,化学反应 2.0H,以86%的收率获得产物n-丙炔基邻苯二甲酸胺
参考文献:一锅烯复分解/ Diels-Alder反应用于构建高度官能化的新型多环氮杂化合物
标题:一锅烯复分解/ Diels-Alder反应用于构建高度官能化的新型多环氮杂化合物
摘要:使用第一代grubbs催化剂通过酶复分解合成了各种三环服务.乙炔的复分解反应在ch 2 Cl 2的回流过程中顺利进行,催化剂负载量低(3.0 Mol%),三环产物6和16的收率高(72-89%).所得的1,3-二烯经diels-Alder法是多环结构的合适前体.烯炔产物与亲二烯体的一锅rcm / Diels-Alder反应平稳进行,得到多环化合物,为单个环加合物.diels-Alder加合物的结构通过1 H NMR光谱和x射线分析确定.环加合物是通过亲二烯体向二烯中的二烯形成的.内在模式.
DOI:10.1016/j.Tet.2007.11.001

海关参考信息

专利信息


专利号:US-7109377-B2
优先权日:1996-10-16
标 题:Synthesis of combinatorial libraries of compounds reminiscent of natural products
发明人:SCHREIBER STUART L; SHAIR MATTHEW D; TAN DEREK S; FOLEY MICHAEL A; STOCKWELL BRENT R
权利人:HARVARD COLLEGE
摘要:The present invention provides complex compounds reminiscent of natural products and libraries thereof, as well as methods for their production. The inventive compounds and libraries of compounds are reminiscent of natural products in that they contain one or more stereocenters, and a high density and diversity of functionality. In general, the inventive libraries are synthesized from diversifiable scaffold structures, which are synthesized from readily available or easily synthesizable template structures. In certain embodiments, the inventive compounds and libraries are generated from diversifiable scaffolds synthesized from a shikimic acid based epoxyol template. In other embodiments, the inventive compounds and libraries are generated from diversifiable scaffolds synthesized from the pyridine-based template isonicotinamide. The present invention also provides a novel ortho-nitrobenzyl photolinker and a method for its synthesis. Furthermore, the present invention provides methods and kits for determining one or more biological activities of members of the inventive libraries. Additionally, the present invention provides pharmaceutical compositions containing one or more library members.

专利号:US-2003082830-A1
优先权日:1996-10-16
标 题:Synthesis of combinatorial libraries of compounds reminiscent of natural products

专利号:WO-0006525-A9
优先权日:1998-07-25
标题:Synthesis of combinatorial libraries of compounds reminiscent of natural products

专利号:WO-0006525-A2
优先权日:1998-07-25
标 题:Synthesis of combinatorial libraries of compounds reminiscent of natural products

专利号:US-6448443-B1
优先权日:1996-10-16
标 题:Synthesis of combinatorial libraries of compounds reminiscent of natural products

专利号:RU-2071962-C1
优先权日:1987-12-18
标题 :Method of synthesis of triazolo-[4,3-a]-[1,4]-diazepines
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主要参考文献

参考标题:Facile Solid-Phase Ruthenium Assisted Azide-Alkyne Cycloaddition (Ruaac) Utilizing The Cp∗rucl(Cod)-Catalyst
作者:Ebbe Engholm,Nicolai Stuhr-Hansen,Ola Blixt |发布日期:2017.6
摘要:The Ruthenium Assisted Azide-Alkyne Cycloaddition (Ruaac) Reaction Is A Well-Established Method For The Generation Of 1,5- And 1,4,5-Substituted 1,2,3-Triazoles, Which We Have Extended To The Solid-Phase Synthesis Of 1,2,3-Triazole-Peptides. The 1,2,3-Triazole Moieties Were Formed Upon The Reaction Of Alkynes With A Solid-Phase Bound Secondary Azide In The Presence Of The Cp∗rucl(Cod) Catalyst At Room

合成参考文献


摘要:Dong, X.; Liu , H., Science of Synthesis Knowledge Updates, (2019) 3, .
摘要:Tian, T.; Li, Z., Science of Synthesis Knowledge Updates, (2020) 2, 376.
摘要:Tanaka, K.; Shibata, Y., Science of Synthesis: Metal-Catalyzed Cyclization Reactions, (2016) 2, 266.
摘要:Cheng, Z.; Zheng, Y.; Lu, Z., Science of Synthesis: Knowledge Updates, (2023) 1, 344.
摘要:Bertrand, X.; Paquin, J.-F., Science of Synthesis: Modern Strategies in Organofluorine Chemistry, (2025) 2.
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