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{5-[2-(2,4-dichlorophenyl)-vinyl]-3-methyl-isoxazol-4-ylamino}-acetic acid | 1443511-60-1

中文名称
——
中文别名
——
英文名称
{5-[2-(2,4-dichlorophenyl)-vinyl]-3-methyl-isoxazol-4-ylamino}-acetic acid
英文别名
2-[[5-[(E)-2-(2,4-dichlorophenyl)ethenyl]-3-methyl-1,2-oxazol-4-yl]amino]acetic acid
{5-[2-(2,4-dichlorophenyl)-vinyl]-3-methyl-isoxazol-4-ylamino}-acetic acid化学式
CAS
1443511-60-1
化学式
C14H12Cl2N2O3
mdl
——
分子量
327.167
InChiKey
OBGINNURPSJDRO-HWKANZROSA-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:
    570.9±50.0 °C(Predicted)
  • 密度:
    1.490±0.06 g/cm3(Temp: 20 °C; Press: 760 Torr)(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    3.9
  • 重原子数:
    21
  • 可旋转键数:
    5
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.14
  • 拓扑面积:
    75.4
  • 氢给体数:
    2
  • 氢受体数:
    5

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

反应信息

  • 作为反应物:
    描述:
    {5-[2-(2,4-dichlorophenyl)-vinyl]-3-methyl-isoxazol-4-ylamino}-acetic acid靛红1,4-萘醌 在 ammonium cerium (IV) nitrate 、 氧气 作用下, 以 乙醇 为溶剂, 反应 0.5h, 以94%的产率得到(E)-2-(5-(2,4-dichlorostyryl)-3-methylisoxazol-4-yl)-2,3-dihydrospiro[benzo[f]isoindole-1,3'-indoline]-2',4,9-trione
    参考文献:
    名称:
    A facile synthesis, anti-inflammatory and analgesic activity of isoxazolyl-2,3-dihydrospiro[benzo[f]isoindole-1,3′-indoline]-2′,4,9-triones
    摘要:
    A new series of isoxazolyl-2,3-dihydrospiro[benzo[f]isoindole-1,3'-indoline]-2',4,9-triones (14) were synthesized by reaction of 4-amino-3-methyl-5-styrylisoxazole 10 with chloroacetic acid followed by a three component reaction with substituted isatins 12 and 1,4-naphthoquinone 13 using Ceric ammonium nitrate (CAN) catalyst under aerial oxidation condition. Structures of these compounds were established on the basis of IR, H-1 NMR, C-13 NMR and mass spectral data. The title compounds 14a-j were evaluated for their anti-inflammatory and analgesic activity. Compounds 14d, 14e and 14f exhibited potent anti-inflammatory and analgesic activity as that of standard drugs. (c) 2013 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2013.04.053
  • 作为产物:
    描述:
    5-(2,4-Dichlorostyryl)-3-methylisoxazol-4-amine氯乙酸二氯甲烷 为溶剂, 反应 2.0h, 以78%的产率得到{5-[2-(2,4-dichlorophenyl)-vinyl]-3-methyl-isoxazol-4-ylamino}-acetic acid
    参考文献:
    名称:
    A facile synthesis, anti-inflammatory and analgesic activity of isoxazolyl-2,3-dihydrospiro[benzo[f]isoindole-1,3′-indoline]-2′,4,9-triones
    摘要:
    A new series of isoxazolyl-2,3-dihydrospiro[benzo[f]isoindole-1,3'-indoline]-2',4,9-triones (14) were synthesized by reaction of 4-amino-3-methyl-5-styrylisoxazole 10 with chloroacetic acid followed by a three component reaction with substituted isatins 12 and 1,4-naphthoquinone 13 using Ceric ammonium nitrate (CAN) catalyst under aerial oxidation condition. Structures of these compounds were established on the basis of IR, H-1 NMR, C-13 NMR and mass spectral data. The title compounds 14a-j were evaluated for their anti-inflammatory and analgesic activity. Compounds 14d, 14e and 14f exhibited potent anti-inflammatory and analgesic activity as that of standard drugs. (c) 2013 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2013.04.053
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文献信息

  • A facile synthesis, anti-inflammatory and analgesic activity of isoxazolyl-2,3-dihydrospiro[benzo[f]isoindole-1,3′-indoline]-2′,4,9-triones
    作者:E. Rajanarendar、S. Ramakrishna、K. Govardhan Reddy、D. Nagaraju、Y.N. Reddy
    DOI:10.1016/j.bmcl.2013.04.053
    日期:2013.7
    A new series of isoxazolyl-2,3-dihydrospiro[benzo[f]isoindole-1,3'-indoline]-2',4,9-triones (14) were synthesized by reaction of 4-amino-3-methyl-5-styrylisoxazole 10 with chloroacetic acid followed by a three component reaction with substituted isatins 12 and 1,4-naphthoquinone 13 using Ceric ammonium nitrate (CAN) catalyst under aerial oxidation condition. Structures of these compounds were established on the basis of IR, H-1 NMR, C-13 NMR and mass spectral data. The title compounds 14a-j were evaluated for their anti-inflammatory and analgesic activity. Compounds 14d, 14e and 14f exhibited potent anti-inflammatory and analgesic activity as that of standard drugs. (c) 2013 Elsevier Ltd. All rights reserved.
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