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3-chloro-4-(4-ethylpiperazin-1-yl)aniline | 626223-64-1

中文名称
——
中文别名
——
英文名称
3-chloro-4-(4-ethylpiperazin-1-yl)aniline
英文别名
——
3-chloro-4-(4-ethylpiperazin-1-yl)aniline化学式
CAS
626223-64-1
化学式
C12H18ClN3
mdl
MFCD03848247
分子量
239.748
InChiKey
OGIDRFDLWCRRNN-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):
    2.2
  • 重原子数:
    16
  • 可旋转键数:
    2
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.5
  • 拓扑面积:
    32.5
  • 氢给体数:
    1
  • 氢受体数:
    3

上下游信息

  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量
    • 1
    • 2

反应信息

  • 作为反应物:
    描述:
    3-chloro-4-(4-ethylpiperazin-1-yl)aniline3-(三氟甲基)苯甲酰氯 在 polymer-supported DIEA 、 polymer-supported trisamine 作用下, 以 二氯甲烷 为溶剂, 生成 N-(3-chloro-4-(4-ethylpiperazin-1-yl)phenyl)-3-(trifluoromethyl)benzamide
    参考文献:
    名称:
    Synthesis and SAR of N-(4-(4-alklylpiperazin-1-yl)phenyl)benzamides as muscarinic acetylcholine receptor subtype 1 (M1) anatgonists
    摘要:
    This Letter describes the synthesis and SAR, developed through an iterative analog library approach, of a novel series of selective M-1 mAChR antagonists, based on an N-(4-(4-alkylpiperazin-1-yl)phenyl)benzamide scaffold for the potential treatment of Parkinson's disease, dystonia and other movement disorders. Compounds in this series possess M-1 antagonist IC(50)s in the 350 nM to >10 mu M range with varying degrees of functional selectivity versus M-2-M-5. (C) 2010 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2010.02.041
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文献信息

  • [EN] PYRROLO[2,3-D]PYRIMIDINE DERIVATIVES AND THEIR USE IN THE TREATMENT OF CANCER<br/>[FR] DÉRIVÉS DE PYRROLO[2,3-D]PYRIMIDINE ET LEUR UTILISATION DANS LE TRAITEMENT DU CANCER
    申请人:SENTINEL ONCOLOGY LTD
    公开号:WO2021074251A1
    公开(公告)日:2021-04-22
    The invention provides compounds of the formula (1): or a salt or tautomer thereof wherein A, R1, R2, R3, R4, R5 and R6 are as defined herein. The compounds are inhibitors of Wee1 and/or PLK1 kinase and are envisaged to be useful in the treatment of cancers.
    这项发明提供了式(1)的化合物:或其盐或互变异构体,其中A、R1、R2、R3、R4、R5和R6如本文所定义。这些化合物是Wee1和/或PLK1激酶的抑制剂,预计在癌症治疗中有用。
  • 1,3-Dihydro-Imidazo [4,5-C] Quinolin-2-Ones as Lipid Kinase Inhibitors
    申请人:Garcia-Echeverria Carlos
    公开号:US20080194579A1
    公开(公告)日:2008-08-14
    The invention relates to novel organic compounds of formula (I) processes for the preparation thereof, the application thereof in a process for the treatment of the human or animal body, the use thereof—alone or in combination with one or more other pharmaceutically active compounds—for the treatment of an inflammatory or obstructive airway disease, such as asthma, disorders commonly occurring in connection with transplantation, or a proliferative disease, such as a tumor disease.
    本发明涉及公式(I)的新有机化合物,其制备方法,其在治疗人体或动物的过程中的应用,其单独或与一种或多种其他药物活性化合物结合使用,用于治疗炎症或阻塞性呼吸道疾病,如哮喘,与移植相关的常见疾病或增生性疾病,如肿瘤疾病。
  • 1,3-DIHYDRO-IMIDAZO[4,5-C]QUINOLIN-2-ONES AS LIPID KINASE INHIBITORS
    申请人:Garcia-Echeverria Carlos
    公开号:US20100056558A1
    公开(公告)日:2010-03-04
    The invention relates to novel organic compounds of formula (I) processes for the preparation thereof, the application thereof in a process for the treatment of the human or animal body, the use thereof—alone or in combination with one or more other pharmaceutically active compounds—for the treatment of an inflammatory or obstructive airway disease, such as asthma, disorders commonly occurring in connection with transplantation, or a proliferative disease, such as a tumor disease.
    本发明涉及公式(I)的新有机化合物,其制备方法,其在处理人或动物体的过程中的应用,其单独使用或与一个或多个其他药物活性化合物结合使用,用于治疗炎症或阻塞性呼吸道疾病,如哮喘,与移植有关的常见疾病或增生性疾病,如肿瘤疾病。
  • Imidazoquinolines as lipid kinase inhibitors
    申请人:Garcia-Echeverria Carlos
    公开号:US20120207751A1
    公开(公告)日:2012-08-16
    The invention relates to a combination comprising compounds of formula (I) and one or more other antiproliferative compounds, hormones or radiation, pharmaceutical preparations comprising the combination thereof, and the application thereof in a process for the treatment of tumors.
    本发明涉及一种组合物,包括式(I)的化合物和一种或多种其他抗增殖化合物、激素或辐射,以及包含该组合物的药物制剂,以及其在肿瘤治疗过程中的应用。
  • 1,3-Dihydro-imidazo[4,5-c]quinolin-2-ones as Lipid Kinase Inhibitors
    申请人:GARCIA-ECHEVERRIA Carlos
    公开号:US20110251202A1
    公开(公告)日:2011-10-13
    The invention relates to novel organic compounds of formula (I) processes for the preparation thereof, the application thereof in a process for the treatment of the human or animal body, the use thereof—alone or in combination with one or more other pharmaceutically active compounds—for the treatment of an inflammatory or obstructive airway disease, such as asthma, disorders commonly occurring in connection with transplantation, or a proliferative disease, such as a tumor disease.
    本发明涉及式(I)的新型有机化合物,其制备方法,其在用于治疗人或动物体内的过程中的应用,其使用-单独或与一种或多种其他药物活性化合物结合使用-用于治疗炎症性或阻塞性呼吸道疾病,如哮喘,与移植有关的常见疾病或增殖性疾病,如肿瘤疾病。
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