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methyl 2-(2-amino-3-pyridyl)-1-(3-methoxypropyl)-1H-benzo[d]imidazole-5-carboxylate | 1430101-82-8

中文名称
——
中文别名
——
英文名称
methyl 2-(2-amino-3-pyridyl)-1-(3-methoxypropyl)-1H-benzo[d]imidazole-5-carboxylate
英文别名
Methyl 2-(2-aminopyridin-3-yl)-1-(3-methoxypropyl)benzimidazole-5-carboxylate;methyl 2-(2-aminopyridin-3-yl)-1-(3-methoxypropyl)benzimidazole-5-carboxylate
methyl 2-(2-amino-3-pyridyl)-1-(3-methoxypropyl)-1H-benzo[d]imidazole-5-carboxylate化学式
CAS
1430101-82-8
化学式
C18H20N4O3
mdl
——
分子量
340.382
InChiKey
VGXJGTOCHMIISP-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):
    1.7
  • 重原子数:
    25
  • 可旋转键数:
    7
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.28
  • 拓扑面积:
    92.3
  • 氢给体数:
    1
  • 氢受体数:
    6

上下游信息

  • 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:
    异氰酸叔丁酯methyl 2-(2-amino-3-pyridyl)-1-(3-methoxypropyl)-1H-benzo[d]imidazole-5-carboxylate苯甲醛scandium tris(trifluoromethanesulfonate) 作用下, 以 neat (no solvent) 为溶剂, 以80%的产率得到methyl 2-[3-(tert-butylamino)-2-phenylimidazo[1,2-a]pyridin-8-yl]-1-(3-methoxypropyl)-1H-benzo[d]imidazole-5-carboxylate
    参考文献:
    名称:
    Multicomponent Solvent-Free Synthesis Of Benzimidazolyl Imidazo[1,2-a]-pyridine Under Microwave Irradiation
    摘要:
    A novel one-pot, three-component reaction employing variously substituted benzimidazole-linked amino pyridines, aldehydes, and isonitriles catalyzed by scandium(III) triflate under solvent-free conditions were accomplished. This new synthetic methodology facilitates the rapid generation of intricate molecular frameworks in three-dimensional fashion leading to benzinaidazole-imidazo [1,2-a] pyridines. This approach is envisioned as an environmentally benign process and a simple operation to the biological interesting compounds. The present synthetic sequence permits the introduction of three points of structural diversity to expand chemical space with high purity and excellent yields.
    DOI:
    10.1021/co400010y
  • 作为产物:
    描述:
    methyl 3-amino-4-[(3-methoxypropyl)amino]benzoate 在 benzotriazol-1-yloxyl-tris-(pyrrolidino)-phosphonium hexafluorophosphate 、 magnesium sulfate 、 三乙胺三氟乙酸 作用下, 以 1,2-二氯乙烷N,N-二甲基甲酰胺 为溶剂, 反应 0.34h, 生成 methyl 2-(2-amino-3-pyridyl)-1-(3-methoxypropyl)-1H-benzo[d]imidazole-5-carboxylate
    参考文献:
    名称:
    Multicomponent Solvent-Free Synthesis Of Benzimidazolyl Imidazo[1,2-a]-pyridine Under Microwave Irradiation
    摘要:
    A novel one-pot, three-component reaction employing variously substituted benzimidazole-linked amino pyridines, aldehydes, and isonitriles catalyzed by scandium(III) triflate under solvent-free conditions were accomplished. This new synthetic methodology facilitates the rapid generation of intricate molecular frameworks in three-dimensional fashion leading to benzinaidazole-imidazo [1,2-a] pyridines. This approach is envisioned as an environmentally benign process and a simple operation to the biological interesting compounds. The present synthetic sequence permits the introduction of three points of structural diversity to expand chemical space with high purity and excellent yields.
    DOI:
    10.1021/co400010y
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文献信息

  • Multicomponent Solvent-Free Synthesis Of Benzimidazolyl Imidazo[1,2-<i>a</i>]-pyridine Under Microwave Irradiation
    作者:Barnali Maiti、Kaushik Chanda、Manikandan Selvaraju、Chih-Chung Tseng、Chung-Ming Sun
    DOI:10.1021/co400010y
    日期:2013.6.10
    A novel one-pot, three-component reaction employing variously substituted benzimidazole-linked amino pyridines, aldehydes, and isonitriles catalyzed by scandium(III) triflate under solvent-free conditions were accomplished. This new synthetic methodology facilitates the rapid generation of intricate molecular frameworks in three-dimensional fashion leading to benzinaidazole-imidazo [1,2-a] pyridines. This approach is envisioned as an environmentally benign process and a simple operation to the biological interesting compounds. The present synthetic sequence permits the introduction of three points of structural diversity to expand chemical space with high purity and excellent yields.
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