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Ethyl 8-methoxycarbonyl-4-oxo-10-propyl-6(4-toluenesulphonamido)-4H-pyrano[3,2-g]quinoline-2-carboxylate | 86694-89-5

中文名称
——
中文别名
——
英文名称
Ethyl 8-methoxycarbonyl-4-oxo-10-propyl-6(4-toluenesulphonamido)-4H-pyrano[3,2-g]quinoline-2-carboxylate
英文别名
2-O-ethyl 8-O-methyl 6-[(4-methylphenyl)sulfonylamino]-4-oxo-10-propylpyrano[3,2-g]quinoline-2,8-dicarboxylate
Ethyl 8-methoxycarbonyl-4-oxo-10-propyl-6(4-toluenesulphonamido)-4H-pyrano[3,2-g]quinoline-2-carboxylate化学式
CAS
86694-89-5
化学式
C27H26N2O8S
mdl
——
分子量
538.578
InChiKey
OJTSDLQWQUEAPA-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:
    718.4±70.0 °C(Predicted)
  • 密度:
    1.383±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    4.7
  • 重原子数:
    38
  • 可旋转键数:
    10
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.26
  • 拓扑面积:
    146
  • 氢给体数:
    1
  • 氢受体数:
    10

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量
  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    参考文献:
    名称:
    Predictive structure-activity relationships in a series of pyranoquinoline derivatives. A new primate model for the identification of antiallergic activity
    摘要:
    A new primate model has been developed for the evaluation of antiallergic agents. Compounds are tested for their ability to inhibit anti-IgE induced histamine release from the bronchoalveolar mast cells lavaged from the lungs of Macaca arctoides infected with the parasite Ascaris suum. A number of 6-substituted pyranoquinoline derivatives have been evaluated and the activities were subjected to Hansch analysis. A highly significant correlation with lipophilicity (pi) and Hammett sigma p values was obtained. The relationship was used to predict further compounds for synthesis giving rise to new, potent analogues. Some apparently anomalous results could be explained by differences in the ionization of, or tautomerism in, the quinoline ring.
    DOI:
    10.1021/jm00402a033
  • 作为产物:
    描述:
    对甲基苯磺酰异氰酸酯2-ethyl 8-methyl 6,9-dihydro-4,6-dioxo-10-propyl-4H-pyrano<3,2-g>quinoline-2,8-dicarboxylate1,1-二氯乙烷 为溶剂, 反应 16.0h, 以to give the sub-title compound as brillant yellow cubes, 44.0 g (82%), m.p. 219° C.的产率得到Ethyl 8-methoxycarbonyl-4-oxo-10-propyl-6(4-toluenesulphonamido)-4H-pyrano[3,2-g]quinoline-2-carboxylate
    参考文献:
    名称:
    Certain hydrolysis or reductive cleavage reaction involving
    摘要:
    本发明涉及一种制备式I的化合物的方法,其中R是氢或烷基Cl至6,而R.sub.5和R.sub.10可以相同也可以不同,分别是氢或烷基Cl至6,或其药学上可接受的衍生物。该方法包括从式II的化合物中去除活化基团,式II为:##STR2##或其适当的衍生物,其中R,R.sub.5和R.sub.10如上所定义,X代表活化基团,并且如果需要,将所得的式I的化合物转化为其药学上可接受的衍生物,或反之亦然。本发明还涉及一种制备式II的化合物的方法,其中R是氢或其适当的衍生物,该方法包括将式III的化合物与式IV的化合物反应,式III为:##STR3##或其适当的衍生物,其中R.sub.5和R.sub.10如上所定义,式IV为X--N.dbd.C.dbd.O,X如上所定义。
    公开号:
    US04471119A1
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文献信息

  • Process for the production of quinoline containing heterocycles, intermediates, and process for the production of the intermediates
    申请人:FISONS plc
    公开号:EP0077090A1
    公开(公告)日:1983-04-20
    There is described a process for the production of a compound of formula 1, in which R is hydrogen or alkyl CI to 6, and R5 and R10, which may be the same or different, are each hydrogen or alkyl CI to 6, or a pharmaceutically acceptable derivative thereof, which comprises removal of an activating group from a compound of formula II, or a suitable derivative thereof, in which R, R5 and R,o are as defined above, and X represents an activating group, and if desired or necessary converting the resulting compound of formula I to a pharmaceutically acceptable derivative thereof, or vice versa. There is also described a process for the production of a compound of formula II in which R is hydrogen, or a suitable derivative thereof, which comprises reaction of a compound of formula III, or a suitable derivative thereof, in which R5 and R10 are as defined above, with a compound of formula IV, in which X is as defined above.
    这里介绍一种生产式 1 化合物的工艺、 其中 R 是氢或 CI-6 烷基,R5 和 R10(可以相同或不同)各自是氢或 CI-6 烷基,或其药学上可接受的衍生物,该工艺包括从式 II.或其适当衍生物中去除活化基团,其中 R、R5 和 R,o 如上文所定义,X 代表活化基团、 或其适当的衍生物,其中 R、R5 和 R,o 如上文所定义,X 代表活化基团,如果需要或必要,将得到的式 I 化合物转化为其药学上可接受的衍生物,反之亦然。 还描述了一种生产式 II 化合物(其中 R 为氢)或其适当衍生物的工艺,该工艺包括式 III、 或其适当衍生物(其中 R5 和 R10 如上文所定义)与式 IV 的化合物反应、 其中 X 如上所定义。
  • A Simple One-Pot Conversion of Alkyl 4-Oxo-1,4-dihydroquinoline-2-carboxylates to 4-Aminoquinoline-2-carboxylates using Reactive Isocyanates
    作者:R. Gordon Mcr. Wright
    DOI:10.1055/s-1984-31080
    日期:——
  • WRIGHT, R. G. MCR., SYNTHESIS, BRD, 1984, N 12, 1058-1061
    作者:WRIGHT, R. G. MCR.
    DOI:——
    日期:——
  • GOULD, KEN J.;MANNERS, CAROL N.;PAYLING, DAVID W.;SUSCHITZKY, JOHN L.;WEL+, J. MED. CHEM., 31,(1988) N 7, 1445-1453
    作者:GOULD, KEN J.、MANNERS, CAROL N.、PAYLING, DAVID W.、SUSCHITZKY, JOHN L.、WEL+
    DOI:——
    日期:——
  • US4471119A
    申请人:——
    公开号:US4471119A
    公开(公告)日:1984-09-11
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