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9-benzylamino-3,3-dimethyl-3,4-dihydroacridine-1(2H)-one | 146351-97-5

中文名称
——
中文别名
——
英文名称
9-benzylamino-3,3-dimethyl-3,4-dihydroacridine-1(2H)-one
英文别名
9-(benzylamino)-3,3-dimethyl-3,4-dihydroacridin-1(2H)-one;9-(benzylamino)-3,3-dimethyl-2,4-dihydroacridin-1-one
9-benzylamino-3,3-dimethyl-3,4-dihydroacridine-1(2H)-one化学式
CAS
146351-97-5
化学式
C22H22N2O
mdl
MFCD00690560
分子量
330.429
InChiKey
UFEQPHYISGZSKN-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

物化性质

  • 沸点:
    522.9±50.0 °C(Predicted)
  • 密度:
    1.185±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    5.2
  • 重原子数:
    25
  • 可旋转键数:
    3
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.27
  • 拓扑面积:
    42
  • 氢给体数:
    1
  • 氢受体数:
    3

文献信息

  • DERIVATIVES OF 9-AMINOACRIDINE HAVING PSYCHOTROPIC, ANTIAMNESTIC AND LIPID REGULATING PROPERTIES
    申请人:VSESOJUZNY NAUCHNY TSENTR PO BEZOPASNOTI BIOLOGICHESKI ACTIVNYKH VESHCHESTV
    公开号:EP0633251A1
    公开(公告)日:1995-01-11
    New chemical compounds, derivatives of 9-aminoacridine of general formula (I) where R = H, CH₃; R¹ = H, CH₃, Br; R² = H, CH₃; R³ = alkyl-C₁-C₅, arylmethyl, diethylaminoethyl; X = C = O, CHOH; Y = CH₂; X + Y = CH = CH; and their salts with organic and non-organic acids. The desired compounds are obtained by interaction of substituted nitriles of antranyl acid with dimedone with subsequent cyclization of intermediate enaminonitriles into corresponding ketones of 9-aminoacridine after the reduction of which and of their derivatives alkylated or aralkylated on the 9-amino group, the corresponding alcohols are obtained, after hydration of which 9-amino-3,4-dihydroacridines are obtained. When experimented on animals, the said derivatives of 9-aminoacridine have shown psychotropic, antiamnestic and lipid regulating properties, as well as a lower toxicity in comparison with known preparations.
    新的化合物,是9-蒽醌的衍生物,其通式为(I),其中R = H、CH₃;R¹ = H、CH₃、Br;R² = H、CH₃;R³ = 烷基-C₁-C₅、芳基甲基、二乙基乙基;X = C = O、CHOH;Y = CH₂;X + Y = CH = CH;以及它们与有机和非有机酸的盐。所需化合物是通过将替代的酰胺基酸腈与二甲酮反应,随后将中间体烯胺腈环化成相应的9-蒽醌酮,还原后得到它们及其衍生物烷基化或芳基烷基化的相应醇,合后得到9-基-3,4-二氢蒽醌。在动物实验中,所述9-蒽醌的衍生物表现出精神药理、抗遗忘和调脂作用,并且与已知制剂相比毒性更低。
  • US5672707A
    申请人:——
    公开号:US5672707A
    公开(公告)日:1997-09-30
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