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2-(4-amino-3-(1-ethynyl)phenyl)acetonitrile | 1220285-09-5

中文名称
——
中文别名
——
英文名称
2-(4-amino-3-(1-ethynyl)phenyl)acetonitrile
英文别名
2-(4-Amino-3-ethynylphenyl)acetonitrile
2-(4-amino-3-(1-ethynyl)phenyl)acetonitrile化学式
CAS
1220285-09-5
化学式
C10H8N2
mdl
——
分子量
156.187
InChiKey
UOKHBJHPONZIQO-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):
    1.1
  • 重原子数:
    12
  • 可旋转键数:
    2
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.1
  • 拓扑面积:
    49.8
  • 氢给体数:
    1
  • 氢受体数:
    2

反应信息

  • 作为反应物:
    描述:
    4-戊炔-1-醇2-(4-amino-3-(1-ethynyl)phenyl)acetonitrile三苯基膦氯金silver trifluoromethanesulfonate 作用下, 以 1,2-二氯乙烷 为溶剂, 反应 12.0h, 以71%的产率得到(3-(2-methyltetrahydro-2-furanyl)-1H-5-indolyl)methyl cyanide
    参考文献:
    名称:
    Gold(I)-catalyzed one-pot reaction between 2-alkynylanilines and alkynols leading to the formation of C-3-substituted indoles: a case of formal carboamination of alkynes
    摘要:
    A process involving gold(I)-catalyzed formal carboamination of alkynes for the synthesis of C-3-substituted indoles has been developed. The procedure utilizes easily accessible starting materials such as 2-alkynylanilines and alkynols. A series of C-3-functionalized indoles are accessible by using this one-pot strategy. Mechanistically, the reaction involves three catalytic cycles and each of them is essentially catalyzed by a single metal catalyst, that is, Ph3PAuOTf. (C) 2010 Published by Elsevier Ltd.
    DOI:
    10.1016/j.tetlet.2010.01.036
  • 作为产物:
    描述:
    potassium carbonate 作用下, 以 甲醇 为溶剂, 反应 1.0h, 以92%的产率得到2-(4-amino-3-(1-ethynyl)phenyl)acetonitrile
    参考文献:
    名称:
    Gold(I)-catalyzed one-pot reaction between 2-alkynylanilines and alkynols leading to the formation of C-3-substituted indoles: a case of formal carboamination of alkynes
    摘要:
    A process involving gold(I)-catalyzed formal carboamination of alkynes for the synthesis of C-3-substituted indoles has been developed. The procedure utilizes easily accessible starting materials such as 2-alkynylanilines and alkynols. A series of C-3-functionalized indoles are accessible by using this one-pot strategy. Mechanistically, the reaction involves three catalytic cycles and each of them is essentially catalyzed by a single metal catalyst, that is, Ph3PAuOTf. (C) 2010 Published by Elsevier Ltd.
    DOI:
    10.1016/j.tetlet.2010.01.036
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