摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

1-(6-chloro-3-pyridinyl)-4-ethylpiperazine | 364794-24-1

中文名称
——
中文别名
——
英文名称
1-(6-chloro-3-pyridinyl)-4-ethylpiperazine
英文别名
1-(6-Chloropyridin-3-yl)-4-ethylpiperazine
1-(6-chloro-3-pyridinyl)-4-ethylpiperazine化学式
CAS
364794-24-1
化学式
C11H16ClN3
mdl
——
分子量
225.721
InChiKey
WWZHDNWJZVUYRA-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

物化性质

  • 沸点:
    352.1±42.0 °C(Predicted)
  • 密度:
    1.154±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    2.1
  • 重原子数:
    15
  • 可旋转键数:
    2
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.55
  • 拓扑面积:
    19.4
  • 氢给体数:
    0
  • 氢受体数:
    3

反应信息

  • 作为反应物:
    描述:
    1-(6-chloro-3-pyridinyl)-4-ethylpiperazine 以 phosphorus tribromide 、 乙酸乙酯 为溶剂, 以940 mg (87%)的产率得到1-(6-bromo-3-pyridinyl)-4-ethylpiperazine
    参考文献:
    名称:
    3-cyanoquinolines, 3-cyano-1,6-naphthyridines, and 3-cyano-1,7-naphthyridines as protein kinase inhibitors
    摘要:
    这项发明提供了具有结构的化合物(I)的公式, 其中T、Z、X、A、R 1 、R 2a 、R 2b 、R 2c 、R 3 、R 4 和n在此处定义,或其药学上可接受的盐,这些化合物可用作抗肿瘤药物,并用于骨质疏松症和多囊肾病的治疗。
    公开号:
    US20020026052A1
  • 作为产物:
    描述:
    N-乙基哌嗪5-溴-2-氯吡啶tris-(dibenzylideneacetone)dipalladium(0)2-二环己膦基-2'-(N,N-二甲胺)-联苯sodium t-butanolate 作用下, 以 乙酸乙酯甲苯 为溶剂, 以269 mg (60%)的产率得到1-(6-chloro-3-pyridinyl)-4-ethylpiperazine
    参考文献:
    名称:
    3-cyanoquinolines, 3-cyano-1,6-naphthyridines, and 3-cyano-1,7-naphthyridines as protein kinase inhibitors
    摘要:
    这项发明提供了具有结构的化合物(I)的公式, 其中T、Z、X、A、R 1 、R 2a 、R 2b 、R 2c 、R 3 、R 4 和n在此处定义,或其药学上可接受的盐,这些化合物可用作抗肿瘤药物,并用于骨质疏松症和多囊肾病的治疗。
    公开号:
    US20020026052A1
点击查看最新优质反应信息

文献信息

  • [EN] 3-CYANOQUINOLINES,3-CYANO-1,6-NAPHTHYRIDINES, AND 3-CYANO-1,7-NAPHTHYRIDINES AS PROTEIN KINASE INHIBITORS<br/>[FR] 3-CYANOQUINOLINES,3-CYANO-1,6-NAPHTHYRIDINES ET 3-CYANO-1,7-NAPHTHYRIDINES UTILISEES COMME INHIBITEURS DE PROTEINEKINASE
    申请人:AMERICAN HOME PROD
    公开号:WO2001072711A1
    公开(公告)日:2001-10-04
    Compounds of Formula (I), having the structure or a pharmaceutically salt thereof are useful as antineoplastic agents and in the treatment of osteoporosis and polycystic kidney disease.
    具有结构式(I)或其药物盐的化合物在抗肿瘤药物和治疗骨质疏松症和多囊肾病方面是有用的。
  • Pyridylamino substituted heterotricyclic compounds, and preparation method and pharmaceutical use thereof
    申请人:SHANGHAI HAIYAN PHARMACEUTICAL TECHNOLOGY CO., LTD.
    公开号:US11168088B2
    公开(公告)日:2021-11-09
    The present disclosure relates to pyridinamine-substituted heterotricyclo compounds, a preparation method thereof, and a use thereof in medicines. Specifically, a compound of formula (I), or a pharmaceutically acceptable salt, stereoisomer, solvate, or prodrug thereof, a preparation method and a use thereof are disclosed, wherein the groups in the formula (I) are as defined in the Description and claims.
    本公开涉及吡啶胺取代的杂环化合物、其制备方法及其在药物中的用途。具体地说,本发明公开了一种式(I)化合物或其药学上可接受的盐、立体异构体、溶液剂或原药,以及其制备方法和用途,其中式(I)中的基团如说明书和权利要求书中所定义。
  • 3-CYANOQUINOLINES,3-CYANO-1,6-NAPHTHYRIDINES, AND 3-CYANO-1,7-NAPHTHYRIDINES AS PROTEIN KINASE INHIBITORS
    申请人:Wyeth
    公开号:EP1268431A1
    公开(公告)日:2003-01-02
  • 3-Cyanoquinolines,3-cyano-1,6-naphthyridines, and 3-cyano-1,7-naphthyridines as protein kinase inhibitors
    申请人:Wyeth
    公开号:US20040176602A1
    公开(公告)日:2004-09-09
    This invention provides compounds of Formula (I), having the structure 1 where T, Z, X, A, R 1 , R 2a , R 2b , R 2c , R 3 , R 4 , and n are defined herein, or a pharmaceutically acceptable salt thereof which are useful as antineoplastic agents and in the treatment of osteoporosis and polycystic kidney disease.
  • PYRIDYLAMINO SUBSTITUTED HETEROTRICYCLIC COMPOUNDS, AND PREPARATION METHOD AND PHARMACEUTICAL USE THEREOF
    申请人:SHANGHAI HAIYAN PHARMACEUTICAL TECHNOLOGY CO., LTD.
    公开号:US20200039983A1
    公开(公告)日:2020-02-06
    The present disclosure relates to pyridinamine-substituted heterotricyclo compounds, a preparation method thereof, and a use thereof in medicines. Specifically, a compound of formula (I), or a pharmaceutically acceptable salt, stereoisomer, solvate, or prodrug thereof, a preparation method and a use thereof are disclosed, wherein the groups in the formula (I) are as defined in the Description and claims.
查看更多