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9,9'-(1,4-phenylene)bis(10-(4-chlorophenyl)-3,3,6,6-tetramethyl-3,4,6,7-tetrahydroacridine-1,8(2H,5H,9H,10H)-dione) | 1221445-66-4

中文名称
——
中文别名
——
英文名称
9,9'-(1,4-phenylene)bis(10-(4-chlorophenyl)-3,3,6,6-tetramethyl-3,4,6,7-tetrahydroacridine-1,8(2H,5H,9H,10H)-dione)
英文别名
9,9'-(1,4-Phenylene)bis(10-(4-chlorophenyl)-3,3,6,6-tetramethyl-3,4,6,7-tetrahydroacridine-1,8(2h,5h,9h,10h)-dione);10-(4-chlorophenyl)-9-[4-[10-(4-chlorophenyl)-3,3,6,6-tetramethyl-1,8-dioxo-4,5,7,9-tetrahydro-2H-acridin-9-yl]phenyl]-3,3,6,6-tetramethyl-4,5,7,9-tetrahydro-2H-acridine-1,8-dione
9,9'-(1,4-phenylene)bis(10-(4-chlorophenyl)-3,3,6,6-tetramethyl-3,4,6,7-tetrahydroacridine-1,8(2H,5H,9H,10H)-dione)化学式
CAS
1221445-66-4
化学式
C52H54Cl2N2O4
mdl
——
分子量
841.918
InChiKey
MKLHZUUYQFAOEK-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):
    10.7
  • 重原子数:
    60
  • 可旋转键数:
    4
  • 环数:
    9.0
  • sp3杂化的碳原子比例:
    0.42
  • 拓扑面积:
    74.8
  • 氢给体数:
    0
  • 氢受体数:
    6

反应信息

  • 作为产物:
    描述:
    对苯二甲醛对氯苯胺5,5-二甲基-1,3-环己二酮 在 1-methylimidazolium tricyanomethanide 作用下, 以 neat (no solvent) 为溶剂, 反应 0.5h, 以93%的产率得到9,9'-(1,4-phenylene)bis(10-(4-chlorophenyl)-3,3,6,6-tetramethyl-3,4,6,7-tetrahydroacridine-1,8(2H,5H,9H,10H)-dione)
    参考文献:
    名称:
    一种使用1-甲基咪唑三氰胺{[HMIM] C(CN)3 }作为纳米结构熔融盐催化剂合成1,8-二氧杂硼氢化hydro啶衍生物的简便方法
    摘要:
    达到为1,8- dioxodecahydroacridine衍生物的合成的实用和方便的方法通过在1-甲基咪唑三氰基{[HMIM存在环状1,3-二酮,醛和各种苯胺或乙酸铵的一锅缩合反应] C(CN)3 }在室温下为纳米结构熔盐(NMS)催化剂。在目前的工作中,将首次报告三十多种产品。
    DOI:
    10.1016/j.molliq.2016.03.006
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文献信息

  • Synthesis and antimicrobial activities of novel bisacridine-1,8-dione derivatives
    作者:Muharrem Kaya、Yılmaz Yıldırır、Gökçen Y. Çelik
    DOI:10.1007/s00044-010-9321-6
    日期:2011.4
    A series of bisacridine-1,8-dione derivatives were synthesized by one-pot reaction of aromatic dialdehydes, dimedone or cyclohexane-1,3-dione and primer aromatic amines in acetonitrile to utilizing Amberlyst-15 as a heterogeneous catalyst. The structures of compounds were characterized by FT-IR, NMR, and elemental analysis. Antimicrobial activities of these compounds were determined by using the disc diffusion method against to these gram-positive and gram-negative bacteria and yeast. The results were compared with reference discs.
  • A convenient method for the synthesis of 1,8-dioxodecahydroacridine derivatives using 1-methylimidazolium tricyanomethanide {[HMIM]C(CN)3} as a nanostructured molten salt catalyst
    作者:Mohammad Ali Zolfigol、Neda Bahrami-Nejad、Saeed Baghery
    DOI:10.1016/j.molliq.2016.03.006
    日期:2016.6
    A practical and convenient method for the synthesis of 1,8-dioxodecahydroacridine derivatives was achieved via the one-pot condensation reaction of cyclic 1,3-diketone, aldehydes and various anilines or ammonium acetate in the presence of 1-methylimidazolium tricyanomethanide [HMIM]C(CN)3} as a nanostructured molten salt (NMS) catalyst at room temperature. In the present work, more than thirty products
    达到为1,8- dioxodecahydroacridine衍生物的合成的实用和方便的方法通过在1-甲基咪唑三氰基[HMIM存在环状1,3-二酮,醛和各种苯胺或乙酸铵的一锅缩合反应] C(CN)3 }在室温下为纳米结构熔盐(NMS)催化剂。在目前的工作中,将首次报告三十多种产品。
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