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3-ethyl-6-phenylpyridazine | 68206-06-4

中文名称
——
中文别名
——
英文名称
3-ethyl-6-phenylpyridazine
英文别名
3-Aethyl-6-phenyl-pyridazin
3-ethyl-6-phenylpyridazine化学式
CAS
68206-06-4
化学式
C12H12N2
mdl
——
分子量
184.241
InChiKey
LQUWCIFAXIXJIN-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):
    2.3
  • 重原子数:
    14
  • 可旋转键数:
    2
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.17
  • 拓扑面积:
    25.8
  • 氢给体数:
    0
  • 氢受体数:
    2

反应信息

  • 作为产物:
    描述:
    在 indium(III) triflate 、 hydrazine hydrate 作用下, 以 1,4-二氧六环 为溶剂, 反应 4.0h, 以73%的产率得到3-ethyl-6-phenylpyridazine
    参考文献:
    名称:
    In(OTf)3-mediated synthesis of substituted pyridazines
    摘要:
    In(OTf)(3) (4c)-mediated one-pot (4+2) cyclocondensation of gamma-alkynones 3 with N2H4(aq) in dioxane affords substituted pyridazines 5 in good yields via a sequential desulfonative or dehydrogenative aromatization. The facile transformation proceeds by a facile synthetic sequence starting with an alpha-propargylation of beta-ketosulfones 1 and a cyclocondensation of gamma-alkynones 3 with N2H4(aq). The method provides a mild and efficient condition. Moreover, this route can be enlarged to multigram scale. (C) 2015 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tet.2015.07.025
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文献信息

  • QUINUCLIDINE COMPOUNDS AS ALPHA-7 NICOTINIC ACETYLCHOLINE RECEPTOR LIGANDS
    申请人:Cook, II James H.
    公开号:US20090270405A1
    公开(公告)日:2009-10-29
    The disclosure provides compounds of formula I, including their salts, as well as compositions and methods of using the compounds. The compounds are ligands for the nicotinic α7 receptor and may be useful for the treatment of various disorders of the central nervous system, especially affective and neurodegenerative disorders.
    该披露提供了公式I的化合物,包括它们的盐,以及使用这些化合物的组合物和方法。这些化合物是烟碱性α7受体的配体,可能对治疗中枢神经系统的各种疾病,特别是情感和神经退行性疾病,有用。
  • Quinuclidine Compounds as Alpha-7 Nicotinic Acetylcholine Receptor Ligands
    申请人:Bristol-Myers Squibb Company
    公开号:US20130131064A1
    公开(公告)日:2013-05-23
    The disclosure provides compounds of formula I, including their salts, as well as compositions and methods of using the compounds. The compounds are ligands for the nicotinic α7 receptor and may be useful for the treatment of various disorders of the central nervous system, especially affective and neurodegenerative disorders.
    本披露提供了I式化合物及其盐,以及使用这些化合物的组合物和方法。这些化合物是尼古丁α7受体的配体,可能有助于治疗中枢神经系统的各种疾病,尤其是情感和神经退行性疾病。
  • US7863291B2
    申请人:——
    公开号:US7863291B2
    公开(公告)日:2011-01-04
  • In(OTf)3-mediated synthesis of substituted pyridazines
    作者:Meng-Yang Chang、Yi-Ju Lu、Yu-Chieh Cheng
    DOI:10.1016/j.tet.2015.07.025
    日期:2015.9
    In(OTf)(3) (4c)-mediated one-pot (4+2) cyclocondensation of gamma-alkynones 3 with N2H4(aq) in dioxane affords substituted pyridazines 5 in good yields via a sequential desulfonative or dehydrogenative aromatization. The facile transformation proceeds by a facile synthetic sequence starting with an alpha-propargylation of beta-ketosulfones 1 and a cyclocondensation of gamma-alkynones 3 with N2H4(aq). The method provides a mild and efficient condition. Moreover, this route can be enlarged to multigram scale. (C) 2015 Elsevier Ltd. All rights reserved.
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