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N-Naphthalen-1-ylmethyl-benzamidine | 198065-85-9

中文名称
——
中文别名
——
英文名称
N-Naphthalen-1-ylmethyl-benzamidine
英文别名
N'-(naphthalen-1-ylmethyl)benzenecarboximidamide
N-Naphthalen-1-ylmethyl-benzamidine化学式
CAS
198065-85-9
化学式
C18H16N2
mdl
——
分子量
260.338
InChiKey
XPCPINGFIGQJTH-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):
    3.7
  • 重原子数:
    20
  • 可旋转键数:
    3
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.06
  • 拓扑面积:
    38.4
  • 氢给体数:
    1
  • 氢受体数:
    1

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:
    2-bromo-3-(1-methylethoxy)-2-propenalN-Naphthalen-1-ylmethyl-benzamidinepotassium carbonate 作用下, 以 氯仿 为溶剂, 反应 18.0h, 以35%的产率得到3-Naphthalen-1-ylmethyl-2-phenyl-3H-imidazole-4-carbaldehyde
    参考文献:
    名称:
    A New Regioselective Synthesis of 1,2,5-Trisubstituted 1H-Imidazoles and Its Application to the Development of Eprosartan
    摘要:
    A new method is presented for the preparation of 1,2-disubstitued-1H-imidazole-5-carboxaldehydes by the reaction of N-monosubstituted amidines with 2-halo-3-alkoxy-2-propenals. The reaction is highly regioselective with ratios of 1,2,5:1,2,4-imidazolecarboxaldehydes ranging from 85:15 to 100: 0. This methodology could be extended with similar results to the synthesis of imidazole-g-nitriles by the reaction of 2-bromo-3-methoxy-2-propenenitrile with N-monosubstituted amidines.
    DOI:
    10.1021/jo971304f
  • 作为产物:
    描述:
    1-萘甲基胺Methyl benzimidate三乙胺 作用下, 以 N,N-二甲基甲酰胺 为溶剂, 反应 16.0h, 生成 N-Naphthalen-1-ylmethyl-benzamidine
    参考文献:
    名称:
    A New Regioselective Synthesis of 1,2,5-Trisubstituted 1H-Imidazoles and Its Application to the Development of Eprosartan
    摘要:
    A new method is presented for the preparation of 1,2-disubstitued-1H-imidazole-5-carboxaldehydes by the reaction of N-monosubstituted amidines with 2-halo-3-alkoxy-2-propenals. The reaction is highly regioselective with ratios of 1,2,5:1,2,4-imidazolecarboxaldehydes ranging from 85:15 to 100: 0. This methodology could be extended with similar results to the synthesis of imidazole-g-nitriles by the reaction of 2-bromo-3-methoxy-2-propenenitrile with N-monosubstituted amidines.
    DOI:
    10.1021/jo971304f
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文献信息

  • A New Regioselective Synthesis of 1,2,5-Trisubstituted 1<i>H</i>-Imidazoles and Its Application to the Development of Eprosartan
    作者:Susan C. Shilcrat、Mohamed K. Mokhallalati、Joseph M. D. Fortunak、Lendon N. Pridgen
    DOI:10.1021/jo971304f
    日期:1997.11.1
    A new method is presented for the preparation of 1,2-disubstitued-1H-imidazole-5-carboxaldehydes by the reaction of N-monosubstituted amidines with 2-halo-3-alkoxy-2-propenals. The reaction is highly regioselective with ratios of 1,2,5:1,2,4-imidazolecarboxaldehydes ranging from 85:15 to 100: 0. This methodology could be extended with similar results to the synthesis of imidazole-g-nitriles by the reaction of 2-bromo-3-methoxy-2-propenenitrile with N-monosubstituted amidines.
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