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    • 54. 发明公开
    • 폴리메틴 체인에 메조-반응작용기를 갖는 신규한 시아닌 유도체 및 이의 제조방법
    • 在聚四氟乙烯链上具有MESO反应性官能团的新型氰胺衍生物及其制备方法
    • KR1020130124265A
    • 2013-11-13
    • KR1020130126581
    • 2013-10-23
    • 이화여자대학교 산학협력단
    • 윤주영지콴궈
    • G01N31/22G01N21/78C07D403/10
    • The present invention relates to a novel cyanine derivative having a meso-reactive functional group at a polymethine chain and a method for manufacturing thereof and the cyanine derivative in which a reactive functional group is displaced at the meso position according to the present invention is suited or mass production because a synthesis method is simple. A reagent for nerve agent detection passes two reactive processes, but the cyanine derivative according to the present invention passes a reactive process of one step only. Therefore, in case of the cyanine derivative, a reaction speed is fast and the sensitivity is excellent and the vitalization is possible in acid PH. The cyanine derivative is able to be used in aqueous environment and is able to be used as an acid pH-activatable ratiometric NIR probe.
    • 本发明涉及一种在聚甲炔链上具有内反应性官能团的新颖花青衍生物及其制备方法,其中反应性官能团在本发明的介观位置上位移的花青衍生物是适用的或 大量生产因为合成方法简单。 用于神经毒素检测的试剂通过两种反应性方法,但根据本发明的花青衍生物仅通过一步反应过程。 因此,在花青衍生物的情况下,反应速度快,灵敏度优异,酸PH可能发生活化。 花青衍生物能够在水性环境中使用,并且能够用作酸可pH活化的比率NIR探针。
    • 55. 发明公开
    • 폴리메틴 체인에 메조-반응작용기를 갖는 신규한 시아닌 유도체 및 이의 제조방법
    • 在聚四氟乙烯链上具有MESO反应性官能团的新型氰胺衍生物及其制备方法
    • KR1020130085755A
    • 2013-07-30
    • KR1020120006796
    • 2012-01-20
    • 이화여자대학교 산학협력단
    • 윤주영지콴궈
    • C07D403/10C07D209/08G01N21/80
    • G01N31/221C07D209/14C07D403/08C09B23/0041C09B23/0066G01N33/84Y10T436/163333
    • PURPOSE: A novel cyanine derivative having meso-reaction functional group in a polymethine chain is provided to give fast reaction rate and excellent sensitivity by passing through only one-step reaction process and to be useful as acidic pH activatable ratiometric NIR probe. CONSTITUTION: A novel cyanine derivative having meso-reaction functional group in a polymethine chain is presented as a chemical formula 1. A manufacturing method of the above mentioned cyanine derivative comprises a step (step 1) obtaining a compound 2 which has a substituted phthalimide at the meso position of compound 3 by reacting compound 3 and phthalimide potassium in the first solvent; and a step (step 2) obtaining compound 1 which has substituted X is at the meso position of compound 2 by reacting compound 2 manufactured in step 1 and X-NH2 in the second solvent as shown in reaction equation 1. The first solvent is one selected from the group of dimethylformamide, dimethylacetamide, diethylether, tetrahydrofuran, 1,4-dioxane, benzene, and toluene.
    • 目的:提供一种在聚甲炔链中具有内消旋反应官能团的新颖花青衍生物,通过仅通过一步反应过程提供快速反应速率和极好的灵敏度,可用作酸性pH活化比例的NIR探针。 构成:在聚甲炔链中具有内消旋反应官能团的新颖花青衍生物作为化学式1表示。上述花青衍生物的制造方法包括步骤(步骤1)得到具有取代的邻苯二甲酰亚胺的化合物2 通过化合物3和邻苯二甲酰亚胺钾在第一溶剂中反应化合物3的内消旋位置; 得到化合物1的步骤(步骤2),如反应式1所示,通过使在步骤1中制造的化合物2和第二溶剂中的X-NH 2反应,得到化合物2的中间位置的化合物1。第一溶剂为 选自二甲基甲酰胺,二甲基乙酰胺,二乙醚,四氢呋喃,1,4-二恶烷,苯和甲苯。
    • 59. 发明公开
    • 바이나프틸기를 갖는 로다민 유도체, 이의 제조방법 및 이를 이용한 구리 이온의 검출방법
    • 罗丹明衍生轴承二甲基集团,其制备方法及使用该组合物检测铜离子的方法
    • KR1020100025891A
    • 2010-03-10
    • KR1020080084637
    • 2008-08-28
    • 이화여자대학교 산학협력단
    • 윤주영첸샤오챵조민정김관묵박성수
    • C07D311/88C07D209/32
    • PURPOSE: A method for detecting copper ion using rhodamine derivative having binaphthyl group is provided to react the rhodamine derivative with copper ion and quantitatively and qualitatively analyze the copper ion. CONSTITUTION: A rhodamine derivative having a binaphthyl group is denoted by chemical formula 1 or 2. A method for preparing the rhodamine derivative having binaphthyl group of chemical formula 1 comprises: a step of adding THF in which potassium hydroxide solution and phenta(ethylene glycol)-ditoxylate are dissolved in 2,2'-dihydroxy-1,1'-binaphtyl-3-carboxadehyde of chemical formula 3 and reacting under reflux condition to obtain 3-formyl-2,2'-binaphthyl-20-crown-6 of chemical formula 4(step 1); a step of adding ethanol solution in which rhodamine B hydrazide of chemical formula 5 in 3-formyl-2,2'-binaphthyl-20-crown-6 of chemical formula 4 and reacting under reflex condition to obtain a compound of chemical formula 1(step 2); and a step of adding ethanol solution and reacting under reflux condition to rhodamine derivative having binaphthyl group of chemical formula 2.
    • 目的:提供使用具有联萘基的罗丹明衍生物检测铜离子的方法,使罗丹明衍生物与铜离子反应,并定量和定性分析铜离子。 构成:具有联萘基的罗丹明衍生物由化学式1或2表示。一种制备具有化学式1的联萘基的罗丹明衍生物的方法包括:加入其中氢氧化钾溶液和苯乙酸(乙二醇)的THF的步骤, - 二氧化物溶于化学式3的2,2'-二羟基-1,1'-联吡啶-3-甲醛中,在回流条件下反应,得到3-甲酰基-2,2'-联萘-20-冠-6 化学式4(步骤1); 将化学式5的罗丹明B酰肼加入到化学式4的3-甲酰基-2,2'-联萘基-20-冠-6中的乙醇溶液的步骤中,并在反应条件下反应,得到化学式1的化合物 第2步); 并加入乙醇溶液并在回流条件下与具有化学式2的联萘基的罗丹明衍生物反应的步骤。
    • 60. 发明公开
    • NBD계 유도체, 이의 제조방법 및 이를 이용한 아연이온의 검출방법
    • 基于NBD的衍生物,其制备方法以及使用该方法检测锌离子的方法
    • KR1020090128737A
    • 2009-12-16
    • KR1020080054640
    • 2008-06-11
    • 이화여자대학교 산학협력단
    • 윤주영츄,차오차오김건희신인재조민정
    • C07D403/14C07D271/12
    • PURPOSE: A method for detecting zinc ion using NBD system derivative is provided to ensure high selectivity to zinc ion under the presence of calcium ion. CONSTITUTION: An NBD(7-nitrobenz-2-oxa-1,3-diazole) system derivative is denoted by chemical formula 1. A method for preparing the NBD system derivative comprises: a step of adding 2-pyridinecarboxaldehyde of chemical formula 2 to methanol solution of ethan-1,2-diamine of chemical formula 2; a step of adding NaBH4 to prepare N,N'-bis(2-pyridylmethyl)-ethan-1,2-diamine of chemical formula 4; a step of adding a compound of chemical formula 4 and NBD-Cl of chemical formula 5 to react at room temperature to produce a compound of chemical formula 6; and a step of adding 2-(bromomethyl)pyridine hydrobromic acid of chemical formula 7 to obtain a compound of chemical formula 1.
    • 目的:提供使用NBD系统衍生物检测锌离子的方法,以确保在钙离子存在下对锌离子的高选择性。 构成:NBD(7-硝基苯并-2-氧杂-1,3-二唑)系统衍生物由化学式1表示。一种制备NBD体系衍生物的方法包括:将化学式2的2-吡啶甲醛加入到 化学式2的乙-1,2-二胺的甲醇溶液; 加入NaBH 4以制备化学式4的N,N'-双(2-吡啶基甲基) - 乙-1,2-二胺的步骤; 将化学式5的化合物和化学式5的NBD-Cl的化合物在室温下反应以制备化学式6的化合物的步骤; 和加入化学式7的2-(溴甲基)吡啶氢溴酸的步骤,得到化学式1的化合物。