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1-(1-(4-bromophenyl)-4-(4-methoxyphenyl)-2-methyl-1H-pyrrol-3-yl)ethanone | 1208334-50-2

中文名称
——
中文别名
——
英文名称
1-(1-(4-bromophenyl)-4-(4-methoxyphenyl)-2-methyl-1H-pyrrol-3-yl)ethanone
英文别名
1-[1-(4-Bromophenyl)-4-(4-methoxyphenyl)-2-methylpyrrol-3-yl]ethanone
1-(1-(4-bromophenyl)-4-(4-methoxyphenyl)-2-methyl-1H-pyrrol-3-yl)ethanone化学式
CAS
1208334-50-2
化学式
C20H18BrNO2
mdl
——
分子量
384.272
InChiKey
QDPILBQXOLEVBT-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):
    4.7
  • 重原子数:
    24
  • 可旋转键数:
    4
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.15
  • 拓扑面积:
    31.2
  • 氢给体数:
    0
  • 氢受体数:
    2

反应信息

  • 作为产物:
    描述:
    1-(4-甲氧苯基)-2-硝基乙烯乙酰丙酮4-溴苯胺 在 iron(III) chloride 作用下, 以 硝基甲烷 为溶剂, 反应 7.0h, 以84%的产率得到1-(1-(4-bromophenyl)-4-(4-methoxyphenyl)-2-methyl-1H-pyrrol-3-yl)ethanone
    参考文献:
    名称:
    氯化铁催化三组分偶联合成多取代的N-芳基吡咯
    摘要:
    摘要描述了在可持续和环境友好的金属催化剂 FeCl3 存在下,高效且操作简单的三组分偶联合成各种 N-芳基取代吡咯。该方法提供了一种直接的方法,用于从易于获得的起始材料(如硝基烯烃、1,3-二羰基化合物和伯芳香胺)以良好的收率合成 N-芳基取代的吡咯。该反应通过 Fe(III) 催化的胺化/迈克尔/环异构化反应的催化序列进行。补充材料可用于本文。转至出版商的 Synthetic Communications® 在线版以查看免费的补充文件。图形概要
    DOI:
    10.1080/00397911.2011.650273
点击查看最新优质反应信息

文献信息

  • The acidic ionic liquid [BSO<sub>3</sub>HMIm]HSO<sub>4</sub>: a novel and efficient catalyst for one-pot, three-component syntheses of substituted pyrroles
    作者:Yuan Luo、Bao-Qiang Zhang、Yan-Hong He、Zhi Guan
    DOI:10.1515/znb-2014-0108
    日期:2015.1.1
    was used as an efficient catalyst for the synthesis of a variety of pyrrole derivatives via a one-pot, three-component condensation of amines, nitroolefins, and 1,3-dicarbonyl compounds. Good to excellent yields of 72–96% were obtained under reflux in ethanol. The catalyst could easily be recovered and recycled up to six times, resulting in good yields without prolonging the reaction time. This method
    摘要 酸性离子液体 3-甲基-2-(1-磺丁基)-1H-咪唑硫酸氢盐 [BSO3HMIm]HSO4 被用作一种有效的催化剂,通过一锅、三胺、硝基烯烃和 1,3-二羰基化合物的组分缩合。在乙醇中回流下获得了 72-96% 的良好收率。催化剂可以很容易地回收和循环使用多达六次,从而在不延长反应时间的情况下获得良好的收率。这种方法在大规模制备中也是有效的。该程序可以很容易地扩展为一锅四组分反应。这种离子液体催化的反应为吡咯生物的合成提供了一种环境友好的替代方法。
  • Iron(III)-Catalyzed Four-Component Coupling Reaction of 1,3-Dicarbonyl Compounds, Amines, Aldehydes, and Nitroalkanes: A Simple and Direct Synthesis of Functionalized Pyrroles
    作者:Sukhendu Maiti、Srijit Biswas、Umasish Jana
    DOI:10.1021/jo902661y
    日期:2010.3.5
    A simple, convenient, and multicomponent coupling strategy for the synthesis of highly functionalized pyrroles catalyzed by iron(III) salts has been developed. This strategy demonstrated four-component coupling reactions of 1,3-dicarbonyl compounds, amines, aromatic aldehydes, and nitroalkanes without an inert atmosphere. This methodology provides an alternative approach for easy access of highly substituted
    已经开发出一种简单,方便和多组分的偶联策略,用于合成(III)盐催化的高度官能化的吡咯。该策略证明了1,3-二羰基化合物,胺,芳族醛和硝基烷的四组分偶联反应无需惰性气氛。这种方法学提供了一种替代方法,可通过一锅串联反应,使用四个简单易用的构建基块,以中等到非常高的收率轻松获得高度取代的吡咯。值得注意的是,与现有方法相比,该方法非常便宜,直接且对环境友好。
  • [Bmim]HSO4 loaded on Graphene Oxide: A Green and Retrievable Nanocatalyst for the Synthesis of Polysubstituted Pyrroles; Some of Which are Fluorinated
    作者:Maral Shekarchi、Farahnaz K. Behbahani
    DOI:10.2174/1570178617999200601170128
    日期:2021.3
    <p>1-Butyl-3-methylimidazolium hydrogen sulfate [bmim]HSO<sub>4</sub> as a non-halogenated ionic liquid was loaded on graphene oxide ([bmim]HSO<sub>4</sub>/GO) and employed as a green, reusable, solid nanocatalyst for the preparation of polysubstituted pyrroles in the presence of amines (such as benzeneamine, 2-amino-4-methylthiazole, adenine (9H-purin-6-amine)), benzaldehydes or cinnamaldehyde or furfural, 1,3-dicarbonyl compounds, and nitromethane at 90-95°C. The advantages of this protocol are the synthesis of some novel polysubstituted pyrroles containing fluorine atoms, thiazole and adenine nuclei that are very important in pharmaceutical and drug discovery research in comparison to previously reported results.</p></sec></div> <div class="value-text ch">1-丁基-3-甲基<a href=https://www.molaid.com/MS_52697 target="_blank">咪唑</a><a href=https://www.molaid.com/MS_37639 target="_blank">氢硫酸盐</a>[bmim]HSO<sub>4</sub>作为一种非卤化<a href=https://www.molaid.com/fenzi/4437 target="_blank">离子液体</a>被加载到氧化<a href=https://www.molaid.com/fenzi/4322 target="_blank">石墨烯</a>([bmim]HSO<sub>4</sub>/GO)上,并作为一种绿色、可重复使用的固体纳米催化剂,用于在<a href=https://www.molaid.com/MS_37224 target="_blank">氨</a>基(如<a href=https://www.molaid.com/MS_10829 target="_blank">苯胺</a>、<a href=https://www.molaid.com/MS_303334 target="_blank">2-氨基-4-甲基噻唑</a>、<a href=https://www.molaid.com/MS_15842 target="_blank">腺嘌呤</a>(9H-<a href=https://www.molaid.com/MS_51494 target="_blank">嘌呤</a>-6-胺))、<a href=https://www.molaid.com/MS_11107 target="_blank">苯甲醛</a>或<a href=https://www.molaid.com/MS_16816 target="_blank">肉桂醛</a>或<a href=https://www.molaid.com/MS_18895 target="_blank">糠醛</a>、1,3-二羰基化合物和<a href=https://www.molaid.com/MS_22319 target="_blank">硝基甲烷</a>存在的条件下在90-95°C下制备多取代<a href=https://www.molaid.com/MS_54252 target="_blank">吡咯</a>。该方法的优点在于合成一些新型含<a href=https://www.molaid.com/MS_38453 target="_blank">氟</a>原子、<a href=https://www.molaid.com/MS_51010 target="_blank">噻唑</a>和<a href=https://www.molaid.com/MS_15842 target="_blank">腺嘌呤</a>核的多取代<a href=https://www.molaid.com/MS_54252 target="_blank">吡咯</a>,与先前报道的结果相比,在制药和药物发现研究中具有重要意义。</div> </div> </li> <li class="feature-list-item"> <div class="content-title">Efficient, Three-Component Synthesis of Pyrrole Derivatives Catalyzed by Iodobenzene and Oxone</div> <div class="value"> <div class="value-text"> <span>作者:</span>Prashant B. Jagadhane、Nikhil C. Jadhav、Omkar P. Herlekar、Vikas N. Telvekar </div> <div class="value-text"> <span>DOI:</span>10.1080/00397911.2015.1066392 </div> <div class="value-text"> <span>日期:</span>2015.9.17 </div> <div class="value-text en">A simple and highly efficient three-component method using easily available amines, nitrostyrene, and diketones in one pot has been developed for synthesis of pyrroles in the presence of catalytic amounts of iodobenzene and Oxone as oxidant. The protocol has been used to afford wide range of pyrroles in moderate to good yields.</div> <div class="value-text ch"></div> </div> </li> </ul> <a href="https://chem.molaid.com/material/detail?source=UserSourcePortal&id=310193ar80ed278157N0&inchikey=QDPILBQXOLEVBT-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_415" class="compound-item" title="黄胆红酸">黄胆红酸</a> <a target="_blank" href="https://www.molaid.com/MS_923" class="compound-item" title="高树蛙毒素">高树蛙毒素</a> <a target="_blank" href="https://www.molaid.com/MS_1418" class="compound-item" title="颜料红2254">颜料红2254</a> <a target="_blank" href="https://www.molaid.com/MS_3010" class="compound-item" title="阿根诺卡菌素">阿根诺卡菌素</a> <a target="_blank" href="https://www.molaid.com/MS_3139" class="compound-item" 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href="https://www.molaid.com/fenzi/22" class="compound-item" title="碳氢化合物">碳氢化合物</a> <a href="https://www.molaid.com/fenzi/23" class="compound-item" title="有机卤素化合物">有机卤素化合物</a> <a href="https://www.molaid.com/fenzi/27" class="compound-item" title="有机磷化合物">有机磷化合物</a> <a href="https://www.molaid.com/fenzi/31" class="compound-item" title="有机盐">有机盐</a> <a href="https://www.molaid.com/fenzi/13" class="compound-item" title="苯丙烷和聚酮">苯丙烷和聚酮</a> <a href="https://www.molaid.com/fenzi/25" class="compound-item" title="有机金属化合物">有机金属化合物</a> </div> </div> </div> <div class="right"> <div class="module"> <link rel="stylesheet" href="https://www-buffer.molaid.com/assets/css/common/hot-molecular.css?v=202505121"> <div class="component-card hot-molecular-card" style="--color: #FF4539;"> <div class="title"> <h3 class="title-name">热门分子</h3> </div> <div class="card-content"> <ul class="list"> <li class="item item-special" data-sort="TOP" onclick="targetBlank(this)"> <div class="item-img"> <img src="data:image/svg+xml;base64,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" 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