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diethyl 1,4-dihydro-2,6-dimethyl-4-(2-naphthyl)pyridine-3,5-dicarboxylate | 50672-71-4

中文名称
——
中文别名
——
英文名称
diethyl 1,4-dihydro-2,6-dimethyl-4-(2-naphthyl)pyridine-3,5-dicarboxylate
英文别名
diethyl 2,6-dimethyl-4-(naphthalen-2-yl)-1,4-dihydropyridine-3,5-dicarboxylate;diethyl 4-(naphthalen-2-yl)-2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylate;diethyl 4-(naphthalene-2-yl)-2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylate;2,6-dimethyl-4- (2-naphthyl) -3,5-diethoxycarbonyl-1,4-dihydropyridine;2,6-dimethyl-4-naphthalen-2-yl-1,4-dihydro-pyridine-3,5-dicarboxylic acid diethyl ester;2,6-Dimethyl-4-naphthyl-(2)-1,4-dihydro-pyridin-dicarbonsaeure-(3,5)-diethylester;Diethyl 2,6-dimethyl-4-naphthalen-2-yl-1,4-dihydropyridine-3,5-dicarboxylate
diethyl 1,4-dihydro-2,6-dimethyl-4-(2-naphthyl)pyridine-3,5-dicarboxylate化学式
CAS
50672-71-4
化学式
C23H25NO4
mdl
——
分子量
379.456
InChiKey
DNELGQXXLDUVEB-UHFFFAOYSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

计算性质

  • 辛醇/水分配系数(LogP):
    4.5
  • 重原子数:
    28
  • 可旋转键数:
    7
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.3
  • 拓扑面积:
    64.6
  • 氢给体数:
    1
  • 氢受体数:
    5

反应信息

  • 作为反应物:
    描述:
    diethyl 1,4-dihydro-2,6-dimethyl-4-(2-naphthyl)pyridine-3,5-dicarboxylatezirconium(IV) nitrate溶剂黄146 作用下, 反应 0.33h, 以94%的产率得到diethyl 2,6-dimethyl-4-(naphth-2-yl)pyridine-3,5-dicarboxylate
    参考文献:
    名称:
    Sabitha, Gowravaram; Kumar Reddy, G. S. Kiran; Reddy, Ch. Srinivas, Synthesis, 2003, # 8, p. 1267 - 1271
    摘要:
    DOI:
  • 作为产物:
    描述:
    乙酰乙酸乙酯2-萘甲醛 在 ammonium acetate 作用下, 以 neat (no solvent) 为溶剂, 反应 0.25h, 以86%的产率得到diethyl 1,4-dihydro-2,6-dimethyl-4-(2-naphthyl)pyridine-3,5-dicarboxylate
    参考文献:
    名称:
    l-Tyrosine loaded nanoparticles: an efficient catalyst for the synthesis of dicoumarols and Hantzsch 1,4-dihydropyridines
    摘要:
    -酪氨酸载荷的纳米颗粒催化有机反应。
    DOI:
    10.1039/c4ra16627b
点击查看最新优质反应信息

文献信息

  • Urea as an Ammonia Surrogate in the Hantzsch’s Synthesis of Polyhydroquinolines / 1,4-dihydropyridines under Green Reaction Conditions
    作者:G. Dhananjaya、Akula Raghunadh、P. Mahesh Kumar、S. Pulla Reddy、V. Narayana Murthy、Venkateswara Rao Anna、Manojit Pal
    DOI:10.2174/1570178617999200713144504
    日期:2021.3
    <p>Synthesis of polyhydroquinolines via Hantzsch’s multicomponent reaction (MCR) involves the use of a hygroscopic and moderately toxic ammonium salt as one of the key reactants. In our effort, we have found urea as an effective ammonia surrogate when the MCR was performed in the presence of sulphonic acid-functionalized Wang resin (Wang-OSO<sub>3</sub>H) as a polymeric and recoverable acidic catalyst under green conditions. Urea is relatively less hygroscopic/toxic than the commonly used ammonium salts used in this MCR. The methodology afforded a range of polyhydroquinolines in good yields. Depending on the nature of reaction conditions employed, the MCR afforded Biginelli product or 1,4-DHPs when the use of 1,3-diketone was omitted.</p> </sec></div> <div class="value-text ch"><p>通过汉奇多组分反应(MCR)合成聚氢<a href=https://www.molaid.com/MS_51724 target="_blank">喹啉</a>,涉及使用一种吸湿性和中等毒性的<a href=https://www.molaid.com/MS_4410 target="_blank">铵</a>盐作为关键反应物之一。在我们的努力中,我们发现<a href=https://www.molaid.com/MS_45556 target="_blank">尿素</a>在存在<a href=https://www.molaid.com/MS_64419 target="_blank">磺酸</a>基功能化王<a href=https://www.molaid.com/fenzi/4585 target="_blank">树脂</a>(Wang-OSO<sub>3</sub>H)作为聚合物和可回收的酸性催化剂的条件下,作为有效的<a href=https://www.molaid.com/MS_37224 target="_blank">氨</a>替代品。<a href=https://www.molaid.com/MS_45556 target="_blank">尿素</a>比这种MCR中常用的<a href=https://www.molaid.com/MS_4410 target="_blank">铵</a>盐相对更不易吸湿/有毒。该工艺提供了一系列高产率的聚氢<a href=https://www.molaid.com/MS_51724 target="_blank">喹啉</a>。根据所用反应条件的性质,当省略使用1,3-二酮时,MCR会生成Biginelli产物或1,4-<a href=https://www.molaid.com/MS_271138 target="_blank">DHP</a>s。</p></div> </div> </li> <li class="feature-list-item"> <div class="content-title">Magnesium Nitride as a Convenient Source of Ammonia: Preparation of Dihydropyridines</div> <div class="value"> <div class="value-text"> <span>作者:</span>Katy L. Bridgwood、Gemma E. Veitch、Steven V. Ley </div> <div class="value-text"> <span>DOI:</span>10.1021/ol801399w </div> <div class="value-text"> <span>日期:</span>2008.8.21 </div> <div class="value-text en"><span style='color:#ff0000'>Magnesium</span> <span style='color:#ff0000'>nitride</span> (Mg 3N 2) has been investigated for the <span style='color:#ff0000'>preparation</span> of dihydropyridines. This is a commercially available, bench-stable solid that generates ammonia upon treatment with protic solvents. The main features of the process are the facile reaction setup and good yields obtained in the majority of cases.</div> <div class="value-text ch">已经研究了<a href=https://www.molaid.com/MS_23275979 target="_blank">氮化镁</a>(Mg 3N 2)用于制备<a href=https://www.molaid.com/fenzi/5237 target="_blank">二氢吡啶</a>。这是一种可从市场上买到的,板凳稳定的固体,在用质子溶剂处理后会生成<a href=https://www.molaid.com/MS_37224 target="_blank">氨</a>。该方法的主要特点是反应设置简便,在大多数情况下均能获得良好的收率。</div> </div> </li> <li class="feature-list-item"> <div class="content-title">一种新型离子型β-萘酚醛席夫碱锆配合物的 制备方法及应用</div> <div class="value"> <div class="value-text"> <span>申请人:</span>山西医科大学 </div> <div class="value-text"> <span>公开号:</span>CN110483563B </div> <div class="value-text"> <span>公开(公告)日:</span>2021-12-28 </div> <div class="value-text en"></div> <div class="value-text ch">本发明属于催化有机合成技术领域,具体涉及一种新型离子型β‑<a href=https://www.molaid.com/MS_9352 target="_blank">萘酚</a>醛席夫碱<a href=https://www.molaid.com/MS_4241 target="_blank">锆</a>配合物的制备方法及应用。本发明<a href=https://www.molaid.com/MS_4241 target="_blank">锆</a>原子与β‑<a href=https://www.molaid.com/MS_9352 target="_blank">萘酚</a>醛席夫碱<a href=https://www.molaid.com/fenzi/4164 target="_blank">配体</a>以及<a href=https://www.molaid.com/MS_34644 target="_blank">水</a>分子配位,两条<a href=https://www.molaid.com/MS_62895 target="_blank">全氟</a>烷(芳)基<a href=https://www.molaid.com/MS_64419 target="_blank">磺酸</a>基团分别以共价键和离子键与中心原子<a href=https://www.molaid.com/MS_4241 target="_blank">锆</a>结合。将β‑<a href=https://www.molaid.com/MS_9352 target="_blank">萘酚</a>醛席夫碱<a href=https://www.molaid.com/MS_4241 target="_blank">锆</a>二<a href=https://www.molaid.com/MS_36390 target="_blank">氯</a>化物溶解于溶剂中,并在N2保护下,将<a href=https://www.molaid.com/MS_4362 target="_blank">银</a>盐加入,室温下避光反应1‑4h,过滤,滤液加入<a href=https://www.molaid.com/MS_38834 target="_blank">正己烷</a>,直至分层,放入冰箱冷冻24h,析出β‑<a href=https://www.molaid.com/MS_9352 target="_blank">萘酚</a>醛席夫碱<a href=https://www.molaid.com/MS_4241 target="_blank">锆</a>配合物。β‑<a href=https://www.molaid.com/MS_9352 target="_blank">萘酚</a>醛席夫碱<a href=https://www.molaid.com/MS_4241 target="_blank">锆</a>配合物具有高空气稳定性和强<a href=https://www.molaid.com/MS_71830 target="_blank">路易斯酸</a>性,能够高效催化醛,β‑<a href=https://www.molaid.com/MS_5960 target="_blank">酮酯</a>和<a href=https://www.molaid.com/MS_32868 target="_blank">醋酸</a><a href=https://www.molaid.com/MS_4410 target="_blank">铵</a>的Hantzsch反应合成1,4‑二氢<a href=https://www.molaid.com/fenzi/5228 target="_blank">吡啶衍生物</a>。</div> </div> </li> <li class="feature-list-item"> <div class="content-title">SUBSTITUTED HETEROCYCLIC COMPOUNDS</div> <div class="value"> <div class="value-text"> <span>申请人:</span>Abelman Matthew </div> <div class="value-text"> <span>公开号:</span>US20090012103A1 </div> <div class="value-text"> <span>公开(公告)日:</span>2009-01-08 </div> <div class="value-text en">The present invention relates to novel heterocyclic compounds and to their use in the treatment of various disease states, including cardiovascular diseases and diabetes. In particular embodiments, the structure of the compounds is given by Formula (I): wherein Q1, Q2, R2, R3, R4, R5, and R6 are as described herein. The invention also relates to methods for the preparation of the compounds, and to pharmaceutical compositions containing such compounds.</div> <div class="value-text ch">本发明涉及新颖的<a href=https://www.molaid.com/fenzi/4179 target="_blank">杂环化合物</a>及其在治疗各种疾病状态中的应用,包括心血管疾病和糖尿病。在特定实施例中,化合物的结构由公式(I)给出:其中Q1、Q2、R2、R3、R4、R5和R6如本文所述。该发明还涉及制备这些化合物的方法,以及含有这些化合物的药物组合物。</div> </div> </li> <li class="feature-list-item"> <div class="content-title">Synthetic Diethyl 2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylates Induce Apoptosis</div> <div class="value"> <div class="value-text"> <span>作者:</span>Seunghyun Ahn、Youngshim Lee、Jihyun Park、Junho Lee、Soon Y. Shin、Young H. Lee、Dongsoo Koh、Yoongho Lim </div> <div class="value-text"> <span>DOI:</span>10.2174/1573406414666180418143048 </div> <div class="value-text"> <span>日期:</span>2018.11.2 </div> <div class="value-text en">mediated through apoptotic cell death. Conclusion: To obtain chemotherapeutic agents that induce apoptosis, 21 <span style='color:#ff0000'>diethyl</span> 2,6-dimethyl- 1,4-dihydropyridine-3,5-dicarboxylates were designed and synthesized. NMR spectroscopy, ab initio calculations, and X-ray crystallography demonstrated that the <span style='color:#ff0000'>diethyl</span> 2,6-dimethyl-1,4- dihydropyridine-3,5-dicarboxylate derivatives synthesized in this research had symmetric</div> <div class="value-text ch">背景:Hantzsch酯2,6-二甲基-1,4-<a href=https://www.molaid.com/fenzi/5237 target="_blank">二氢吡啶</a>-<a href=https://www.molaid.com/MS_267231 target="_blank">3,5-二羧酸</a>二<a href=https://www.molaid.com/MS_220865 target="_blank">乙酯</a>已被用作<a href=https://www.molaid.com/fenzi/5298 target="_blank">氢化物</a>供体,并且已报道了其多种<a href=https://www.molaid.com/fenzi/4147 target="_blank">生物</a>学效应。为了鉴定具有凋亡作用的<a href=https://www.molaid.com/fenzi/4464 target="_blank">化学</a>治疗剂,设计并合成了21种2,6-二甲基-1,4-<a href=https://www.molaid.com/fenzi/5237 target="_blank">二氢吡啶</a>-<a href=https://www.molaid.com/MS_267231 target="_blank">3,5-二羧酸</a>二<a href=https://www.molaid.com/MS_220865 target="_blank">乙酯</a>;迄今为止,尚未报道它们是凋亡诱导剂。研究了它们的结构-细胞毒性关系。对标题化合物进行了进一步的<a href=https://www.molaid.com/fenzi/4147 target="_blank">生物</a>学实验。 方法:使用克隆形成测定法在HCT116人结肠癌细胞中测定当前合成化合物的细胞毒性。膜联蛋白V染色测定法用于确认标题化合物是否诱导凋亡。为了鉴定合成化合物,进行了核磁共振(NMR)光谱和高分辨率质谱(HR-MS)。由于在NMR光谱数据中观察到分子对称性,因此从头算和X射线晶体学确定了三维结构。 结果:从NMR光谱,从头算和X射线晶体学获得的结果表明,在本研究中合成的2,6-二甲基-1,4-<a href=https://www.molaid.com/fenzi/5237 target="_blank">二氢吡啶</a>-3,5-二<a href=https://www.molaid.com/MS_232084 target="_blank">羧酸</a>二<a href=https://www.molaid.com/MS_220865 target="_blank">乙酯</a>衍<a href=https://www.molaid.com/fenzi/4147 target="_blank">生物</a>具有对称结构。在HCT116人</div> </div> </li> </ul> <a href="https://chem.molaid.com/material/detail?source=UserSourcePortal&id=3101944yaf856d0256M0&inchikey=DNELGQXXLDUVEB-UHFFFAOYSA-N" target="_blank" rel="nofollow" class="view-more">查看更多</a> </div> <div class="module" id="tongleihuahewu"> <h3 class="module-title"><i class="iconfont icon-tongleihuahewu"></i>同类化合物</h3> <div class="compounds-list"> <a target="_blank" href="https://www.molaid.com/MS_22672148" class="compound-item" title="(S)-溴烯醇内酯">(S)-溴烯醇内酯</a> <a target="_blank" href="https://www.molaid.com/MS_68" class="compound-item" title="(R)-3,3''-双([[1,1''-联苯]-4-基)-[1,1''-联萘]-2,2''-二醇">(R)-3,3''-双([[1,1''-联苯]-4-基)-[1,1''-联萘]-2,2''-二醇</a> <a target="_blank" href="https://www.molaid.com/MS_133" class="compound-item" title="(3S,3aR)-2-(3-氯-4-氰基苯基)-3-环戊基-3,3a,4,5-四氢-2H-苯并[g]吲唑-7-羧酸">(3S,3aR)-2-(3-氯-4-氰基苯基)-3-环戊基-3,3a,4,5-四氢-2H-苯并[g]吲唑-7-羧酸</a> <a target="_blank" href="https://www.molaid.com/MS_136" class="compound-item" title="(3R,3’’R,4S,4’’S,11bS,11’’bS)-(+)-4,4’’-二叔丁基-4,4’’,5,5’’-四氢-3,3’’-联-3H-二萘酚[2,1-c:1’’,2’’-e]膦(S)-BINAPINE">(3R,3’’R,4S,4’’S,11bS,11’’bS)-(+)-4,4’’-二叔丁基-4,4’’,5,5’’-四氢-3,3’’-联-3H-二萘酚[2,1-c:1’’,2’’-e]膦(S)-BINAPINE</a> <a target="_blank" href="https://www.molaid.com/MS_201" class="compound-item" title="(11bS)-2,6-双(3,5-二甲基苯基)-4-羟基-4-氧化物-萘并[2,1-d:1'',2''-f][1,3,2]二氧磷">(11bS)-2,6-双(3,5-二甲基苯基)-4-羟基-4-氧化物-萘并[2,1-d:1'',2''-f][1,3,2]二氧磷</a> <a target="_blank" href="https://www.molaid.com/MS_202" class="compound-item" title="(11bS)-2,6-双(3,5-二氯苯基)-4羟基-4-氧-二萘并[2,1-d:1'',2''-f][1,3,2]二氧磷杂七环">(11bS)-2,6-双(3,5-二氯苯基)-4羟基-4-氧-二萘并[2,1-d:1'',2''-f][1,3,2]二氧磷杂七环</a> <a target="_blank" href="https://www.molaid.com/MS_23529102" class="compound-item" title="(11bR)-2,6-双[3,5-双(1,1-二甲基乙基)苯基]-4-羟基-4-氧化物-二萘并[2,1-d:1'',2''-f][1,3,2]二氧杂磷平">(11bR)-2,6-双[3,5-双(1,1-二甲基乙基)苯基]-4-羟基-4-氧化物-二萘并[2,1-d:1'',2''-f][1,3,2]二氧杂磷平</a> <a target="_blank" href="https://www.molaid.com/MS_414" class="compound-item" title="黄胺酸">黄胺酸</a> <a target="_blank" href="https://www.molaid.com/MS_1194" class="compound-item" title="马兜铃对酮">马兜铃对酮</a> <a target="_blank" href="https://www.molaid.com/MS_22031681" class="compound-item" title="马休黄钠盐一水合物">马休黄钠盐一水合物</a> <a target="_blank" href="https://www.molaid.com/MS_1207" class="compound-item" title="马休黄">马休黄</a> <a target="_blank" href="https://www.molaid.com/MS_1354" class="compound-item" title="食品黄6号">食品黄6号</a> <a target="_blank" href="https://www.molaid.com/MS_1355" 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title="颜料红4">颜料红4</a> <a target="_blank" href="https://www.molaid.com/MS_1414" class="compound-item" title="颜料红261">颜料红261</a> <a target="_blank" href="https://www.molaid.com/MS_1415" class="compound-item" title="颜料红258">颜料红258</a> <a target="_blank" href="https://www.molaid.com/MS_1419" class="compound-item" title="颜料红220">颜料红220</a> <a target="_blank" href="https://www.molaid.com/MS_1420" class="compound-item" title="颜料红22">颜料红22</a> <a target="_blank" href="https://www.molaid.com/MS_1421" class="compound-item" title="颜料红214">颜料红214</a> <a target="_blank" href="https://www.molaid.com/MS_1423" class="compound-item" title="颜料红2">颜料红2</a> <a target="_blank" href="https://www.molaid.com/MS_1424" class="compound-item" title="颜料红19">颜料红19</a> <a target="_blank" href="https://www.molaid.com/MS_1426" class="compound-item" title="颜料红185">颜料红185</a> <a target="_blank" href="https://www.molaid.com/MS_1427" class="compound-item" title="颜料红184">颜料红184</a> <a target="_blank" 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src="data:image/svg+xml;base64,PD94bWwgdmVyc2lvbj0iMS4wIiBlbmNvZGluZz0iVVRGLTgiPz4KPHN2ZyB4bWxucz0iaHR0cDovL3d3dy53My5vcmcvMjAwMC9zdmciIHhtbG5zOnhsaW5rPSJodHRwOi8vd3d3LnczLm9yZy8xOTk5L3hsaW5rIiB3aWR0aD0iMzAwIiBoZWlnaHQ9IjMwMCIgdmlld0JveD0iMCAwIDMwMCAzMDAiPgo8ZGVmcz4KPGc+CjxnIGlkPSJnbHlwaC0wLTAiPgo8cGF0aCBkPSJNIDEuNjg3NSA1Ljk4NDM3NSBMIDEuNjg3NSAtMjMuODkwNjI1IEwgMTguNjI1IC0yMy44OTA2MjUgTCAxOC42MjUgNS45ODQzNzUgWiBNIDMuNTkzNzUgNC4xMDkzNzUgTCAxNi43MzQzNzUgNC4xMDkzNzUgTCAxNi43MzQzNzUgLTIxLjk4NDM3NSBMIDMuNTkzNzUgLTIxLjk4NDM3NSBaIE0gMy41OTM3NSA0LjEwOTM3NSAiLz4KPC9nPgo8ZyBpZD0iZ2x5cGgtMC0xIj4KPHBhdGggZD0iTSAzLjMyODEyNSAtMjQuNjg3NSBMIDcuODI4MTI1IC0yNC42ODc1IEwgMTguNzgxMjUgLTQuMDMxMjUgTCAxOC43ODEyNSAtMjQuNjg3NSBMIDIyLjAxNTYyNSAtMjQuNjg3NSBMIDIyLjAxNTYyNSAwIEwgMTcuNTE1NjI1IDAgTCA2LjU2MjUgLTIwLjY1NjI1IEwgNi41NjI1IDAgTCAzLjMyODEyNSAwIFogTSAzLjMyODEyNSAtMjQuNjg3NSAiLz4KPC9nPgo8L2c+CjwvZGVmcz4KPHBhdGggZmlsbD0ibm9uZSIgc3Ryb2tlLXdpZHRoPSIwLjAzMzMzMzMiIHN0cm9rZS1saW5lY2FwPSJidXR0IiBzdHJva2UtbGluZWpvaW49Im1pdGVyIiBzdHJva2U9InJnYigwJSwgMCUsIDAlKSIgc3Ryb2tlLW9wYWNpdHk9IjEiIHN0cm9rZS1taXRlcmxpbWl0PSIxMCIgZD0iTSAxLjcyNDIyOCAwLjQ5NDY5MSBMIDEuNzI0MjI4IDEuNTEzMzExICIgdHJhbnNmb3JtPSJtYXRyaXgoODQuNjgxMDYxLCAwLCAwLCA4NC42ODEwNjEsIDMuNDEyNDU0LCA3Mi4yNzcwMTkpIi8+CjxwYXRoIGZpbGw9Im5vbmUiIHN0cm9rZS13aWR0aD0iMC4wMzMzMzMzIiBzdHJva2UtbGluZWNhcD0iYnV0dCIgc3Ryb2tlLWxpbmVqb2luPSJtaXRlciIgc3Ryb2tlPSJyZ2IoMCUsIDAlLCAwJSkiIHN0cm9rZS1vcGFjaXR5PSIxIiBzdHJva2UtbWl0ZXJsaW1pdD0iMTAiIGQ9Ik0gMS43MTU5MjQgMC41MDkxMjkgTCAyLjMzOTM1NyAwLjE0NzcwOSAiIHRyYW5zZm9ybT0ibWF0cml4KDg0LjY4MTA2MSwgMCwgMCwgODQuNjgxMDYxLCAzLjQxMjQ1NCwgNzIuMjc3MDE5KSIvPgo8cGF0aCBmaWxsPSJub25lIiBzdHJva2Utd2lkdGg9IjAuMDMzMzMzMyIgc3Ryb2tlLWxpbmVjYXA9ImJ1dHQiIHN0cm9rZS1saW5lam9pbj0ibWl0ZXIiIHN0cm9rZT0icmdiKDAlLCAwJSwgMCUpIiBzdHJva2Utb3BhY2l0eT0iMSIgc3Ryb2tlLW1pdGVybGltaXQ9IjEwIiBkPSJNIDEuNzI0MjI4IDAuNTA0Mjg2IEwgMC44NTM0NTEgLTAuMDAzNjQwMzYgIiB0cmFuc2Zvcm09Im1hdHJpeCg4NC42ODEwNjEsIDAsIDAsIDg0LjY4MTA2MSwgMy40MTI0NTQsIDcyLjI3NzAxOSkiLz4KPHBhdGggZmlsbD0ibm9uZSIgc3Ryb2tlLXdpZHRoPSIwLjAzMzMzMzMiIHN0cm9rZS1saW5lY2FwPSJidXR0IiBzdHJva2UtbGluZWpvaW49Im1pdGVyIiBzdHJva2U9InJnYigwJSwgMCUsIDAlKSIgc3Ryb2tlLW9wYWNpdHk9IjEiIHN0cm9rZS1taXRlcmxpbWl0PSIxMCIgZD0iTSAxLjU1NzU2NCAwLjYwMDAwMyBMIDAuODUzMDgyIDAuMTg5MDg2ICIgdHJhbnNmb3JtPSJtYXRyaXgoODQuNjgxMDYxLCAwLCAwLCA4NC42ODEwNjEsIDMuNDEyNDU0LCA3Mi4yNzcwMTkpIi8+CjxwYXRoIGZpbGw9Im5vbmUiIHN0cm9rZS13aWR0aD0iMC4wMzMzMzMzIiBzdHJva2UtbGluZWNhcD0iYnV0dCIgc3Ryb2tlLWxpbmVqb2luPSJtaXRlciIgc3Ryb2tlPSJyZ2IoMCUsIDAlLCAwJSkiIHN0cm9rZS1vcGFjaXR5PSIxIiBzdHJva2UtbWl0ZXJsaW1pdD0iMTAiIGQ9Ik0gMS43MTU5MjQgMS40OTg5MTkgTCAyLjU5ODc0MSAyLjAxMDM1ICIgdHJhbnNmb3JtPSJtYXRyaXgoODQuNjgxMDYxLCAwLCAwLCA4NC42ODEwNjEsIDMuNDEyNDU0LCA3Mi4yNzcwMTkpIi8+CjxwYXRoIGZpbGw9Im5vbmUiIHN0cm9rZS13aWR0aD0iMC4wMzMzMzMzIiBzdHJva2UtbGluZWNhcD0iYnV0dCIgc3Ryb2tlLWxpbmVqb2luPSJtaXRlciIgc3Ryb2tlPSJyZ2IoMCUsIDAlLCAwJSkiIHN0cm9rZS1vcGFjaXR5PSIxIiBzdHJva2UtbWl0ZXJsaW1pdD0iMTAiIGQ9Ik0gMS43MjQyMjggMS41MDM3MTYgTCAwLjg1MTU2IDIuMDAyMzI0ICIgdHJhbnNmb3JtPSJtYXRyaXgoODQuNjgxMDYxLCAwLCAwLCA4NC42ODEwNjEsIDMuNDEyNDU0LCA3Mi4yNzcwMTkpIi8+CjxwYXRoIGZpbGw9Im5vbmUiIHN0cm9rZS13aWR0aD0iMC4wMzMzMzMzIiBzdHJva2UtbGluZWNhcD0iYnV0dCIgc3Ryb2tlLWxpbmVqb2luPSJtaXRlciIgc3Ryb2tlPSJyZ2IoMCUsIDAlLCAwJSkiIHN0cm9rZS1vcGFjaXR5PSIxIiBzdHJva2UtbWl0ZXJsaW1pdD0iMTAiIGQ9Ik0gMS41NTc1NjQgMS40MDY5ODQgTCAwLjg1MjExMyAxLjgxMDAxMiAiIHRyYW5zZm9ybT0ibWF0cml4KDg0LjY4MTA2MSwgMCwgMCwgODQuNjgxMDYxLCAzLjQxMjQ1NCwgNzIuMjc3MDE5KSIvPgo8cGF0aCBmaWxsPSJub25lIiBzdHJva2Utd2lkdGg9IjAuMDMzMzMzMyIgc3Ryb2tlLWxpbmVjYXA9ImJ1dHQiIHN0cm9rZS1saW5lam9pbj0ibWl0ZXIiIHN0cm9rZT0icmdiKDAlLCAwJSwgMCUpIiBzdHJva2Utb3BhY2l0eT0iMSIgc3Ryb2tlLW1pdGVybGltaXQ9IjEwIiBkPSJNIDIuODQ5MTI5IDAuMTQ2NzQgTCAzLjQ3MDQ4NiAwLjUwNDI0ICIgdHJhbnNmb3JtPSJtYXRyaXgoODQuNjgxMDYxLCAwLCAwLCA4NC42ODEwNjEsIDMuNDEyNDU0LCA3Mi4yNzcwMTkpIi8+CjxwYXRoIGZpbGw9Im5vbmUiIHN0cm9rZS13aWR0aD0iMC4wMzMzMzMzIiBzdHJva2UtbGluZWNhcD0iYnV0dCIgc3Ryb2tlLWxpbmVqb2luPSJtaXRlciIgc3Ryb2tlPSJyZ2IoMCUsIDAlLCAwJSkiIHN0cm9rZS1vcGFjaXR5PSIxIiBzdHJva2UtbWl0ZXJsaW1pdD0iMTAiIGQ9Ik0gMi43NjYwMDQgMC4yOTExNyBMIDMuMzAzNzc2IDAuNjAwNjAzICIgdHJhbnNmb3JtPSJtYXRyaXgoODQuNjgxMDYxLCAwLCAwLCA4NC42ODEwNjEsIDMuNDEyNDU0LCA3Mi4yNzcwMTkpIi8+CjxwYXRoIGZpbGw9Im5vbmUiIHN0cm9rZS13aWR0aD0iMC4wMzMzMzMzIiBzdHJva2UtbGluZWNhcD0iYnV0dCIgc3Ryb2tlLWxpbmVqb2luPSJtaXRlciIgc3Ryb2tlPSJyZ2IoMCUsIDAlLCAwJSkiIHN0cm9rZS1vcGFjaXR5PSIxIiBzdHJva2UtbWl0ZXJsaW1pdD0iMTAiIGQ9Ik0gMC44NzAxOTYgLTAuMDAzNTk0MjMgTCAtMC4wMDgzMzAzNCAwLjUwNDI0ICIgdHJhbnNmb3JtPSJtYXRyaXgoODQuNjgxMDYxLCAwLCAwLCA4NC42ODEwNjEsIDMuNDEyNDU0LCA3Mi4yNzcwMTkpIi8+CjxwYXRoIGZpbGw9Im5vbmUiIHN0cm9rZS13aWR0aD0iMC4wMzMzMzMzIiBzdHJva2UtbGluZWNhcD0iYnV0dCIgc3Ryb2tlLWxpbmVqb2luPSJtaXRlciIgc3Ryb2tlPSJyZ2IoMCUsIDAlLCAwJSkiIHN0cm9rZS1vcGFjaXR5PSIxIiBzdHJva2UtbWl0ZXJsaW1pdD0iMTAiIGQ9Ik0gMi41ODIwODggMi4wMTAzNSBMIDMuNDcwNDQgMS40OTc3MTkgIiB0cmFuc2Zvcm09Im1hdHJpeCg4NC42ODEwNjEsIDAsIDAsIDg0LjY4MTA2MSwgMy40MTI0NTQsIDcyLjI3NzAxOSkiLz4KPHBhdGggZmlsbD0ibm9uZSIgc3Ryb2tlLXdpZHRoPSIwLjAzMzMzMzMiIHN0cm9rZS1saW5lY2FwPSJidXR0IiBzdHJva2UtbGluZWpvaW49Im1pdGVyIiBzdHJva2U9InJnYigwJSwgMCUsIDAlKSIgc3Ryb2tlLW9wYWNpdHk9IjEiIHN0cm9rZS1taXRlcmxpbWl0PSIxMCIgZD0iTSAyLjU4MjIyNiAxLjgxNzg1NCBMIDMuMzAzNzc2IDEuNDAxNDk0ICIgdHJhbnNmb3JtPSJtYXRyaXgoODQuNjgxMDYxLCAwLCAwLCA4NC42ODEwNjEsIDMuNDEyNDU0LCA3Mi4yNzcwMTkpIi8+CjxwYXRoIGZpbGw9Im5vbmUiIHN0cm9rZS13aWR0aD0iMC4wMzMzMzMzIiBzdHJva2UtbGluZWNhcD0iYnV0dCIgc3Ryb2tlLWxpbmVqb2luPSJtaXRlciIgc3Ryb2tlPSJyZ2IoMCUsIDAlLCAwJSkiIHN0cm9rZS1vcGFjaXR5PSIxIiBzdHJva2UtbWl0ZXJsaW1pdD0iMTAiIGQ9Ik0gMC44NjgxNjYgMi4wMDIzNyBMIC0wLjAwODMzMDM0IDEuNDk0NjI5ICIgdHJhbnNmb3JtPSJtYXRyaXgoODQuNjgxMDYxLCAwLCAwLCA4NC42ODEwNjEsIDMuNDEyNDU0LCA3Mi4yNzcwMTkpIi8+CjxwYXRoIGZpbGw9Im5vbmUiIHN0cm9rZS13aWR0aD0iMC4wMzMzMzMzIiBzdHJva2UtbGluZWNhcD0iYnV0dCIgc3Ryb2tlLWxpbmVqb2luPSJtaXRlciIgc3Ryb2tlPSJyZ2IoMCUsIDAlLCAwJSkiIHN0cm9rZS1vcGFjaXR5PSIxIiBzdHJva2UtbWl0ZXJsaW1pdD0iMTAiIGQ9Ik0gMy40NjIwOSAwLjQ4OTgwMSBMIDMuNDYyMDkgMS41MTIxNTggIiB0cmFuc2Zvcm09Im1hdHJpeCg4NC42ODEwNjEsIDAsIDAsIDg0LjY4MTA2MSwgMy40MTI0NTQsIDcyLjI3NzAxOSkiLz4KPHBhdGggZmlsbD0ibm9uZSIgc3Ryb2tlLXdpZHRoPSIwLjAzMzMzMzMiIHN0cm9rZS1saW5lY2FwPSJidXR0IiBzdHJva2UtbGluZWpvaW49Im1pdGVyIiBzdHJva2U9InJnYigwJSwgMCUsIDAlKSIgc3Ryb2tlLW9wYWNpdHk9IjEiIHN0cm9rZS1taXRlcmxpbWl0PSIxMCIgZD0iTSAwLjAwMDAxODk5OTIgMC40ODk4MDEgTCAwLjAwMDAxODk5OTIgMS41MDkwMjEgIiB0cmFuc2Zvcm09Im1hdHJpeCg4NC42ODEwNjEsIDAsIDAsIDg0LjY4MTA2MSwgMy40MTI0NTQsIDcyLjI3NzAxOSkiLz4KPHBhdGggZmlsbD0ibm9uZSIgc3Ryb2tlLXdpZHRoPSIwLjAzMzMzMzMiIHN0cm9rZS1saW5lY2FwPSJidXR0IiBzdHJva2UtbGluZWpvaW49Im1pdGVyIiBzdHJva2U9InJnYigwJSwgMCUsIDAlKSIgc3Ryb2tlLW9wYWNpdHk9IjEiIHN0cm9rZS1taXRlcmxpbWl0PSIxMCIgZD0iTSAwLjE2NjY4MyAwLjU4NTk4IEwgMC4xNjY2ODMgMS40MTI5OCAiIHRyYW5zZm9ybT0ibWF0cml4KDg0LjY4MTA2MSwgMCwgMCwgODQuNjgxMDYxLCAzLjQxMjQ1NCwgNzIuMjc3MDE5KSIvPgo8ZyBmaWxsPSJyZ2IoMTklLCAzMSUsIDk3LjAwMDAwMyUpIiBmaWxsLW9wYWNpdHk9IjEiPgo8dXNlIHhsaW5rOmhyZWY9IiNnbHlwaC0wLTEiIHg9IjIxMC40MTQwNjIiIHk9Ijg0LjYyNSIvPgo8L2c+Cjwvc3ZnPgo=" 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