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2-amino-4-(4-hydroxyphenyl)-5-oxo-4H,5H-dihydropyrano[3,2-c]chromene-3-carbonitrile

中文名称
——
中文别名
——
英文名称
2-amino-4-(4-hydroxyphenyl)-5-oxo-4H,5H-dihydropyrano[3,2-c]chromene-3-carbonitrile
英文别名
2-amino-4,5-dihydro-4-(4-hydroxyphenyl)-5-oxopyrano[3,2-c]chromene-3-carbonitrile;2-amino-4,5-dihydro-5-oxo-4-(4-hydroxyphenyl)pyrano[3,2-c]chromene-3-carbonitrile;2-amino-4-(4-hydroxyphenyl)-5-oxo-4,5-dihydropyrano[3,2-c]chromene-3-carbonitrile;2-amino-4-(4-hydroxyphenyl)-5-oxo-4H,5H-pyrano[3,2-c]chromene-3-carbonitrile;2-amino-3-cyano-4-(4-hydroxyphenyl)-4H,5H-pyrano[3,2-c]benzopyran-5-one;2-amino-4-(4-hydroxyphenyl)-4H,5H-pyrano[3,2-c]chromene-3-carbonitrile;2-amino-4-(4-hydroxyphenyl)-5-oxo-4H-pyrano[3,2-c]chromene-3-carbonitrile
2-amino-4-(4-hydroxyphenyl)-5-oxo-4H,5H-dihydropyrano[3,2-c]chromene-3-carbonitrile化学式
CAS
——
化学式
C19H12N2O4
mdl
——
分子量
332.315
InChiKey
XNWKTAYSDXKKJC-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):
    2.7
  • 重原子数:
    25
  • 可旋转键数:
    1
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.05
  • 拓扑面积:
    106
  • 氢给体数:
    2
  • 氢受体数:
    6

反应信息

  • 作为反应物:
    描述:
    2-amino-4-(4-hydroxyphenyl)-5-oxo-4H,5H-dihydropyrano[3,2-c]chromene-3-carbonitrile溶剂黄146 作用下, 生成 1,2-benzo-[1,3-diaza-4-(4-methoxyaniline)-5-(4-hydroxyphenyl)-6-oxo-7,10-dioxa]anthracene
    参考文献:
    名称:
    作为黄嘌呤氧化酶抑制剂的稠合吡喃并[3,2-d]嘧啶衍生物的合成,筛选和对接。
    摘要:
    鉴于开发有效的黄嘌呤氧化酶(XO)酶抑制剂,合成了一系列100种吡喃并[3,2-d]嘧啶衍生物,并对其体外XO酶抑制进行了评估。结构活动关系也已建立。在所有合成的化合物中,发现4d,8d和9d是最有效的酶抑制剂,IC50值分别为8μM,8.5μM和7μM。在酶动力学研究中进一步研究了化合物9d,Lineweaver-Burk图显示化合物9d是混合型抑制剂。还已经计算出最有效的化合物4d,8d和9d的分子性质。进行了对接研究以研究黄嘌呤氧化酶与最有效的XO抑制剂9d之间的识别模式。
    DOI:
    10.1016/j.ejmech.2017.03.002
  • 作为产物:
    参考文献:
    名称:
    在无溶剂和无催化剂条件下,通过多组分串联策略,可见光促进了二氢吡喃并[2,3-c]苯二酚的合成
    摘要:
    首次报道了高度官能化的二氢吡喃并[3,2- c ]苯二酚的光活化,高效,一锅“真实”绿色合成。
    DOI:
    10.1039/c5gc02855h
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文献信息

  • 1-Methylimidazolium tricyanomethanide {[HMIM]C(CN)3} as a nano structure and reusable molten salt catalyst for the synthesis of tetrahydrobenzo[b]pyrans via tandem Knoevenagel-Michael cyclocondensation and 3,4-dihydropyrano[c]chromene derivatives
    作者:Mohammad Ali Zolfigol、Neda Bahrami-Nejad、Fatemeh Afsharnadery、Saeed Baghery
    DOI:10.1016/j.molliq.2016.06.069
    日期:2016.9
    An expeditious, experimentally simple and rapid 1-methylimidazolium tricyanomethanide [HMIM]C(CN)3} nano molten salt (NMS) catalyzed tandem Knoevenagel-Michael cyclocondensation procedure for the synthesis of tetrahydrobenzo[b]pyrans was described via reaction between dimedone, aromatic aldehyde and malononitrile under solvent-free conditions at room temperature. Furthermore, 3,4-dihydropyrano[c]chromene
    通过二甲酮之间的反应,描述了一种快速,实验简单且快速的三氰基甲基1-甲基咪唑鎓[HMIM] C(CN)3 }纳米熔融盐(NMS)催化串联Knoevenagel-Michael环缩合反应合成四氢苯并[ b ]吡喃的方法,室温下在无溶剂条件下的芳族醛和丙二腈。此外,在相同条件下,以[HMIM] C(CN)3 } NMS为催化量,通过4-羟基香豆素,芳香醛和丙二腈的缩合反应合成了3,4-二氢吡喃并[ c ]色烯衍生物。
  • Heterogeneous ditopic ZnFe<sub>2</sub>O<sub>4</sub>catalyzed synthesis of 4H-pyrans: further conversion to 1,4-DHPs and report of functional group interconversion from amide to ester
    作者:Paramita Das、Arghya Dutta、Asim Bhaumik、Chhanda Mukhopadhyay
    DOI:10.1039/c3gc42095g
    日期:——
    Highly stable, environmentally benign ZnFe2O4 nanopowder was prepared, characterized and applied in the one-pot, three-component synthesis of 4H-pyrans in water. The ZnFe2O4 catalyst provides both acidic (Fe3+) and basic functionalities (O2−) as the reaction requires. The advantages of this method lie in its simplicity, cost effectiveness, environmental friendliness and easier scaling up for large scale synthesis. Water was exploited both as a reaction medium as well as a medium for synthesis of the catalyst. Moreover, water was the only byproduct. The present report puts forward an application of 4H-pyrans for the synthesis of 1,4-DHPs. This is the first attempt towards the synthesis of 4H-pyran-3-carboxylate from 4H-pyran-3-carboxamide. The corresponding functional group interconversion from amide to ester is rare in organic synthesis.
    成功制备、表征并应用了一种稳定且对环境友好的ZnFe2O4纳米粉,在水相中实现了4H-吡喃的一锅法三组分合成。ZnFe2O4催化剂同时提供了反应所需的酸性(Fe3+)和碱性(O2−)功能。该方法的优势在于其简单性、成本效益、环境友好性以及更易于放大进行大规模合成。水既被用作反应介质,也被用作催化剂的合成介质。此外,水是唯一的副产品。本报告提出了一种应用4H-吡喃合成1,4-二氢吡啶(1,4-DHPs)的方法。这是首次尝试从4H-吡喃-3-甲酰胺合成4H-吡喃-3-羧酸酯。在有机合成中,从酰胺到酯的功能团转换是罕见的。
  • DBU: a highly efficient catalyst for one-pot synthesis of substituted 3,4-dihydropyrano[3,2-c]chromenes, dihydropyrano[4,3-b]pyranes, 2-amino-4H-benzo[h]chromenes and 2-amino-4H benzo[g]chromenes in aqueous medium
    作者:Jitender M. Khurana、Bhaskara Nand、Pooja Saluja
    DOI:10.1016/j.tet.2010.05.082
    日期:2010.7
    We have reported DBU catalyzed one-pot synthesis of 3,4-dihydropyrano[3,2-c]chromenes, dihydropyrano[4,3-b]pyranes, 2-amino-4H-benzo[h]chromenes and 2-amino-4H-benzo[g]chromenes from aldehydes, active methylene compounds malononitrile/ethyl cyanocacetate, and 4-hydroxycoumarin/4-hydroxy-6-methylpyrone/1-naphthol/2-hydroxynaphthalene-1,4-dione in water under reflux. The attractive features of this process
    我们已经报道了DBU催化一锅合成3,4-二氢吡喃并[3,2- c ]苯并二氢吡喃并[4,3- b ]吡喃,2-氨基-4 H-苯并[ h ]苯并二胺回流下得自醛,活性亚甲基化合物丙二腈/氰基乙酸乙酯和4-羟基香豆素/ 4-羟基-6-甲基吡喃酮/ 1-萘酚/ 2-羟基萘-1,4-二酮的-4 H-苯并[ g ]色酮。该方法的吸引人的特征是温和的反应条件,反应介质的可重​​复使用性,较短的反应时间,易于分离的产物以及优异的产率。
  • Synthesis of a novel dendrimer core of oxo-vanadium phthalocyanine magnetic nano particles: as an efficient catalyst for the synthesis of 3,4-dihydropyrano[c]chromenes derivatives under green condition
    作者:Maliheh Safaiee、Mohammad Ali Zolfigol、Fatemeh Afsharnadery、Saeed Baghery
    DOI:10.1039/c5ra18723k
    日期:——
    Finally, catalytic activity of the prepared Fe3O4@SiO2@SiO2(CH2)3@AVOPc was examined in the synthesis of 3,4-dihydropyrano[c]chromenes derivatives. The nano catalysts provided excellent catalytic activities to yield the desired products in short reaction time, mild and green conditions under solvent-free at room temperature. The catalysts could be easily separated from the reaction mixture by a magnet
    通过将氨基钒氧代酞菁共价结合在具有3-氯丙基部分的二氧化硅包覆的磁铁矿纳米颗粒的表面上,合成了一种新型的可磁性回收的纳米催化剂。使用不同的物理化学方法(例如FT-IR光谱,X射线衍射(XRD),扫描电子显微镜(SEM),透射电子显微镜(TEM),原子力显微镜(AFM)和热重量分析(TGA),能量色散X射线能谱(EDX)和振动样品磁力分析(VSM),Brunauer-Emmett-Teller(BET),X射线荧光(XRF)和电感耦合等离子体(ICP)。最后,制备的Fe 3 O 4 @SiO 2 @SiO 2的催化活性(CH 2)3 @AVOPc在合成3,4-二氢吡喃并[c]色酮衍生物中进行了研究。纳米催化剂提供了出色的催化活性,可在较短的反应时间,温和和绿色条件下于室温下在无溶剂的条件下产生所需的产物。催化剂可以很容易地用磁铁从反应混合物中分离出来,并且可以连续八次循环使用,而不会损失任何
  • A novel magnetically recyclable semi‐dendrimer catalyst‐based ethanolpyridole supported on ferrite nanoparticles (HNPs@Py) for the synthesis of biscoumarin and dihydropyrano[3,2‐ <i>c</i> ]chromene derivatives
    作者:Fatemeh Afsharnadery、Kaveh Khosravi、Mohammad Ali Zolfigol
    DOI:10.1002/aoc.6297
    日期:2021.8
    The novel organic–inorganic nanohybrid magnetic nanoparticles (HNPs@Py) were prepared by a simple method and characterized by FT-IR, XRD, FE-SEM, TGA, VSM, EDX, and MAP. The catalytic activity of this new (HNPs@Py) was studied for green synthesis of biscoumarin and 3,4-dihydropyrano[c]chromene derivatives. The short reaction time, high yields, simple workup, and easy separation of catalyst from the
    通过简单的方法制备了新型有机-无机纳米杂化磁性纳米粒子 (HNPs@Py),并通过 FT-IR、XRD、FE-SEM、TGA、VSM、EDX 和 MAP 进行表征。研究了这种新的 (HNPs@Py) 的催化活性,用于双香豆素和 3,4-二氢吡喃并 [ c ] 色烯衍生物的绿色合成。本协议的主要优点是反应时间短、收率高、后处理简单以及易于从反应混合物中分离催化剂。
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