CAS: 52250-50-7; 1-Phenyl-3,4-Dihydroisoquinoline

该化合物是一种有机化合物,其特征是双环结构,由一个有引信的等离子环系统和一个联苯组组成,通常看起来无色可粉黄黄色液体或固体,视其纯度和形态而定;该化合物以其潜在的生物活动而著称,包括其作为各种药物合成及其在药用化学应用中的前体的作用;其分子结构有助于其特性,例如有机溶剂中的中溶性以及水溶性相对较低;该苯组的存在增强了其脂性,从而可以影响其与生物膜的相互作用;此外,1-phenyl-34-dihyrodioquinline可能具有荧光特性,从而在某些分析应用中有用;与许多有机化合物一样,重要的是谨慎地处理它,同时考虑安全规程可能具有毒性或再活性.

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合成工艺路线路线简述

  • 合成目标产物 1-Phenyl-3,4-Dihydroisoquinoline 主要起始原料 (1R)-Phenyl-1,2,3,4-Tetrahydroisoquinoline
  • (文献来源)合成步骤主要原料 (1R)-Phenyl-1,2,3,4-Tetrahydroisoquinoline
📜Ethyl Benzoyl Carbonate置于phosphorus Pentoxide,三氯氧磷体系中,用 N,N-二甲基甲酰胺,Xylene 作为反应溶剂,化学反应生成 1-苯基-3,4-二氢异喹啉
参考文献:Synthesis Of A High-Efficiency Red Phosphorescent Emitter For Organic Light-Emitting Diodes
标题:Synthesis Of A High-Efficiency Red Phosphorescent Emitter For Organic Light-Emitting Diodes
摘要:合成了四种新型红色磷光发射体化合物:双(1-苯基异喹啉-N,C2')铱(乙酰丙酮),(Piq)2Ir(Acac),双(1-(1'-萘基)异喹啉-N,C2')铱(乙酰丙酮),(1-Niq)2Ir(Acac),双(1-(2'-萘基)异喹啉-N,C2')铱(乙酰丙酮),(2-Niq)2Ir(Acac)和双(1-苯基-5-甲基异喹啉-N,C2')铱(乙酰丙酮),(M-Piq)2Ir(Acac),并对其进行了全面表征.制备了结构为ito/npb/cbp:掺杂剂/bcp/alq3/al的电致发光器件.所有器件在红色区域发射,发射范围从624到680 Nm.(M-Piq)2Ir(Acac)在电流密度j=300 Ma Cm−2时显示出最大亮度17164 Cd M−2,在电流密度j=20 Ma Cm−2时显示出最佳亮度效率8.91 Cd A−1.(1-Niq)2Ir(Acac)表现出纯红色发射,1931Cie(国际照明委员会)色度坐标x=0.701,Y=0.273.
DOI:10.1039/b313843G

海关参考信息

专利信息


专利号:CN-107384885-A
优先权日:2017-09-05
标题:Application of imine reductase and its mutants in the synthesis of (S)-1-aryl-1,2,3,4-tetrahydroisoquinolines

专利号:CN-107384885-B
优先权日:2017-09-05
标 题:Application of imine reductase and mutant thereof in synthesis of (S) -1-aryl-1, 2, 3, 4-tetrahydroisoquinoline

专利号:CN-109355266-B
优先权日:2018-11-06
标题 :Imine reductase mutant and application thereof in synthesis of optically active 1-substituted-tetrahydroisoquinoline derivative

专利号:CN-110041255-A
优先权日:2019-04-28
标 题 :Asymmetric Synthesis of Solifenacin Intermediates

专利号:CN-108329309-A
优先权日:2018-04-17
标 题 :A kind of synthesis process of solifenacin succinate bulk drug

专利号:US-7642357-B2
优先权日:2004-08-27
标 题 :Iridium complexes
发明人:MASHIMA KAZUSHI; YAMAGATA TSUNEAKI
权利人:TAKASAGO PERFUMERY CO LTD
摘要:The present invention has as its object to provide an iridium complex represented by the general formula:n n[(I r H L 1 L 2 ) 2 (μ−X 1 )(μ−X 2 )(μ−X 3 )]X 4   (1)n n(wherein L 1 and L 2 may be the same or different and each represent a monodendate neutral ligand, or each cooperate with the other to form a bidendate neutral ligand; X 1 , X 2 and X 3 may be the same or different, and each represent a halogen atom; and X 4 is a counter-anion). Also, the present invention provides a novel catalyst which can achieve excellent performance as a catalyst for asymmetric synthesis, especially asymmetric hydrogenation, in terms of chemical selectivity, enantioselectivity and catalytic activity, and the like.

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📌 第三方产品分析报告

✅ COA系统入驻 | 共享模式

主要参考文献

参考标题:A Versatile Cyclodehydration Reaction For The Synthesis Of Isoquinoline And β-Carboline Derivatives
作者:Mohammad Movassaghi,Matthew D. Hill |发布日期:2008.8.21
摘要:Beta-Carboline Derivatives Via Mild Electrophilic Amide Activation, With Trifluoromethanesulfonic Anhydride In The Presence Of 2-Chloropyridine, Is Described. Low-Temperature Amide Activation Followed By Cyclodehydration Upon Warming Provides The Desired Products With Short Overall Reaction Times. The Successful Use Of Nonactivated And Halogenated Phenethylene Derived Amides, N-Vinyl Amides, And Optically Active

合成参考文献


摘要:Leipold, F.; Hussain, S.; France, S. P.; Turner, N. J., Science of Synthesis: Biocatalysis in Organic Synthesis, (2015) 2, 359.
摘要:Li, D.-D.; Wang, G.-W., Science of Synthesis: Catalytic Transformations via CH Activation, (2015) 2, 316.
摘要:Li, D.-D.; Wang, G.-W., Science of Synthesis: Catalytic Transformations via CH Activation, (2015) 2, 344.
摘要:Xing, Y.-K.; Fang, P.; Wang, Z.-H.; Mei, T.-S., Science of Synthesis: Special Topics, (2021) 1, 146.
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