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N-(4-chlorophenyl)-5-(4-methoxyphenyl)-1,3,4-oxadiazol-2-amine | 1257256-94-2

中文名称
——
中文别名
——
英文名称
N-(4-chlorophenyl)-5-(4-methoxyphenyl)-1,3,4-oxadiazol-2-amine
英文别名
——
N-(4-chlorophenyl)-5-(4-methoxyphenyl)-1,3,4-oxadiazol-2-amine化学式
CAS
1257256-94-2
化学式
C15H12ClN3O2
mdl
——
分子量
301.732
InChiKey
CDEKUVIQRBCLCA-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):
    3.9
  • 重原子数:
    21
  • 可旋转键数:
    4
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.07
  • 拓扑面积:
    60.2
  • 氢给体数:
    1
  • 氢受体数:
    5

反应信息

  • 作为产物:
    描述:
    p-chlorophenyl isoselenocyanate对甲氧基苯甲酰肼 在 air 作用下, 以 N,N-二甲基甲酰胺 为溶剂, 反应 4.0h, 以94%的产率得到N-(4-chlorophenyl)-5-(4-methoxyphenyl)-1,3,4-oxadiazol-2-amine
    参考文献:
    名称:
    Synthesis of 2-amino-1,3,4-oxadiazoles from isoselenocyanates via cyclodeselenization
    摘要:
    An efficient one-pot method to access 2-amino-1,3,4-oxadiazoles from isoselenocyanates and hydrazides or dihydrazides was developed via cyclodeselenization. Without any harsh reagents, various 2-amino-1,3,4-oxadiazoles were obtained in considerably high yields (82%-97%) and purities (>99%) directly with simple crystallization in ethanol. And the formed precipitated Se powder during the reaction could be recycled for preparation of isoselenocyanates efficiently. A plausible mechanism is proposed for the formation of the target products. (C) 2011 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tet.2011.05.100
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文献信息

  • Synthesis of 2-amino-1,3,4-oxadiazoles from isoselenocyanates via cyclodeselenization
    作者:Yuanyuan Xie、Junli Liu、Ping Yang、Xiangjun Shi、Jianjun Li
    DOI:10.1016/j.tet.2011.05.100
    日期:2011.7
    An efficient one-pot method to access 2-amino-1,3,4-oxadiazoles from isoselenocyanates and hydrazides or dihydrazides was developed via cyclodeselenization. Without any harsh reagents, various 2-amino-1,3,4-oxadiazoles were obtained in considerably high yields (82%-97%) and purities (>99%) directly with simple crystallization in ethanol. And the formed precipitated Se powder during the reaction could be recycled for preparation of isoselenocyanates efficiently. A plausible mechanism is proposed for the formation of the target products. (C) 2011 Elsevier Ltd. All rights reserved.
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