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6-(4-Bromophenyl)-2-[(6-methyl-1-benzofuran-3-yl)methyl]imidazo[2,1-b][1,3,4]thiadiazole-5-carbaldehyde | 1061271-01-9

中文名称
——
中文别名
——
英文名称
6-(4-Bromophenyl)-2-[(6-methyl-1-benzofuran-3-yl)methyl]imidazo[2,1-b][1,3,4]thiadiazole-5-carbaldehyde
英文别名
——
6-(4-Bromophenyl)-2-[(6-methyl-1-benzofuran-3-yl)methyl]imidazo[2,1-b][1,3,4]thiadiazole-5-carbaldehyde化学式
CAS
1061271-01-9
化学式
C21H14BrN3O2S
mdl
——
分子量
452.331
InChiKey
ZFUBYHUTHLIZGL-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):
    5.7
  • 重原子数:
    28
  • 可旋转键数:
    4
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.1
  • 拓扑面积:
    88.6
  • 氢给体数:
    0
  • 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
  • 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:
    描述:
    6-(4-Bromophenyl)-2-[(6-methyl-1-benzofuran-3-yl)methyl]imidazo[2,1-b][1,3,4]thiadiazole-5-carbaldehyde吡啶盐酸羟胺 作用下, 反应 6.0h, 以61%的产率得到6-(4-bromophenyl)-2-(6-methylbenzofuran-3-ylmethyl)-imidazo[2,1-b][1,3,4]thiadiazole-5-carbaldehyde oxime
    参考文献:
    名称:
    Synthesis and anti-inflammatory evaluation of methylene bridged benzofuranyl imidazo[2,1-b][1,3,4]thiadiazoles
    摘要:
    A series of 6-substituted and 5,6-disubstituted 2-(6-methyl-benzofuran-3-ylmethyl)-imidazo[2,1-b] [ 1,3,4]thiadiazoles have been synthesized. The new compounds have been tested for their in vivo analgesic, anti-inflammatory activities. Qualitative SAR studies indicate that the chloro substitution in the imidazole ring and introduction of formyl group at C-5 position of the imidazole ring increased the anti-inflammatory and analgesic activity. All the newly synthesized compounds have been characterized by spectral data and ORTEP diagram of one of the intermediates 6-(4-chlorophenyl)-2-(6-methyl-benzofuran-3-ylmethyl)-5-morpholin-4-ylmethyl imidazo[2,1-b][1,3,4]thiadiazole is reported herein. (c) 2007 Elsevier Masson SAS. All rights reserved.
    DOI:
    10.1016/j.ejmech.2007.06.023
  • 作为产物:
    描述:
    6-(4-Bromophenyl)-2-[(6-methyl-1-benzofuran-3-yl)methyl]imidazo[2,1-b][1,3,4]thiadiazoleN,N-二甲基甲酰胺三氯氧磷 作用下, 以60%的产率得到6-(4-Bromophenyl)-2-[(6-methyl-1-benzofuran-3-yl)methyl]imidazo[2,1-b][1,3,4]thiadiazole-5-carbaldehyde
    参考文献:
    名称:
    Synthesis and anti-inflammatory evaluation of methylene bridged benzofuranyl imidazo[2,1-b][1,3,4]thiadiazoles
    摘要:
    A series of 6-substituted and 5,6-disubstituted 2-(6-methyl-benzofuran-3-ylmethyl)-imidazo[2,1-b] [ 1,3,4]thiadiazoles have been synthesized. The new compounds have been tested for their in vivo analgesic, anti-inflammatory activities. Qualitative SAR studies indicate that the chloro substitution in the imidazole ring and introduction of formyl group at C-5 position of the imidazole ring increased the anti-inflammatory and analgesic activity. All the newly synthesized compounds have been characterized by spectral data and ORTEP diagram of one of the intermediates 6-(4-chlorophenyl)-2-(6-methyl-benzofuran-3-ylmethyl)-5-morpholin-4-ylmethyl imidazo[2,1-b][1,3,4]thiadiazole is reported herein. (c) 2007 Elsevier Masson SAS. All rights reserved.
    DOI:
    10.1016/j.ejmech.2007.06.023
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