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4-(2-{[4-[[3-(4-Chlorophenyl)propyl](methyl)amino]-6-(1-piperazinyl)-1,3,5-triazin-2-yl]amino}ethyl)phenol | 459873-38-2

中文名称
——
中文别名
——
英文名称
4-(2-{[4-[[3-(4-Chlorophenyl)propyl](methyl)amino]-6-(1-piperazinyl)-1,3,5-triazin-2-yl]amino}ethyl)phenol
英文别名
4-[2-[[4-[3-(4-chlorophenyl)propyl-methylamino]-6-piperazin-1-yl-1,3,5-triazin-2-yl]amino]ethyl]phenol
4-(2-{[4-[[3-(4-Chlorophenyl)propyl](methyl)amino]-6-(1-piperazinyl)-1,3,5-triazin-2-yl]amino}ethyl)phenol化学式
CAS
459873-38-2
化学式
C25H32ClN7O
mdl
——
分子量
482.028
InChiKey
HDYBQLAEZFTWNQ-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):
    5.1
  • 重原子数:
    34
  • 可旋转键数:
    10
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.4
  • 拓扑面积:
    89.4
  • 氢给体数:
    3
  • 氢受体数:
    8

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    4-(2-{[4-[[3-(4-Chlorophenyl)propyl](methyl)amino]-6-(1-piperazinyl)-1,3,5-triazin-2-yl]amino}ethyl)phenol苄磺酰氯N,N-二异丙基乙胺 作用下, 以 二氯甲烷乙腈 为溶剂, 反应 5.0h, 生成 4-{2-[4-{[3-(4-Chloro-phenyl)-propyl]-methyl-amino}-6-(4-phenylmethanesulfonyl-piperazin-1-yl)-[1,3,5]triazin-2-ylamino]-ethyl}-phenol
    参考文献:
    名称:
    A New Series of Estrogen Receptor Modulators That Display Selectivity for Estrogen Receptor β
    摘要:
    A series of 1,3,5-triazine-based estrogen receptor (ER) modulators that are modestly selective for the ERbeta subtype are reported. Compound 1, which displayed modest potency and selectivity for ERbeta vs ERalpha, was identified via high-throughput screening utilizing an ERbeta SPA-based binding assay. Subsequent analogue preparation resulted in the identification of compounds such as 21 and 43 that display 25- to 30-fold selectivity for ERbeta with potencies in the 10-30 nM range. These compounds profile as full antagonists at ERbeta and weak partial agonists at ERalpha in a cell-based reporter gene assay. In addition, the X-ray crystal structure of compound 15 complexed with the ligand binding domain of ERbeta has been solved and was utilized in the design of more conformationally restrained analogues such as 31 in an attempt to increase selectivity for the ERbeta subtype.
    DOI:
    10.1021/jm020291h
  • 作为产物:
    参考文献:
    名称:
    A New Series of Estrogen Receptor Modulators That Display Selectivity for Estrogen Receptor β
    摘要:
    A series of 1,3,5-triazine-based estrogen receptor (ER) modulators that are modestly selective for the ERbeta subtype are reported. Compound 1, which displayed modest potency and selectivity for ERbeta vs ERalpha, was identified via high-throughput screening utilizing an ERbeta SPA-based binding assay. Subsequent analogue preparation resulted in the identification of compounds such as 21 and 43 that display 25- to 30-fold selectivity for ERbeta with potencies in the 10-30 nM range. These compounds profile as full antagonists at ERbeta and weak partial agonists at ERalpha in a cell-based reporter gene assay. In addition, the X-ray crystal structure of compound 15 complexed with the ligand binding domain of ERbeta has been solved and was utilized in the design of more conformationally restrained analogues such as 31 in an attempt to increase selectivity for the ERbeta subtype.
    DOI:
    10.1021/jm020291h
  • 作为试剂:
    描述:
    Tert-butyl 4-(4-[[3-(4-chlorophenyl)propyl](methyl)amino]-6-{[2-(4-hydroxyphenyl)ethyl]amino}-1,3,5-triazin-2-yl)-1-piperazinecarboxylate盐酸碳酸氢钠乙酸乙酯magnesium sulfate 、 silica gel 、 hexanes EtOAc 、 chloroform methanol4-(2-{[4-[[3-(4-Chlorophenyl)propyl](methyl)amino]-6-(1-piperazinyl)-1,3,5-triazin-2-yl]amino}ethyl)phenol 作用下, 以 1,4-二氧六环乙酸乙酯乙醚 为溶剂, 25.0~80.0 ℃ 、355.5 kPa 条件下, 反应 18.0h, 以to afford 925 mgs (80%) of the title compound as a white solid的产率得到4-(2-{[4-[[3-(4-Chlorophenyl)propyl](methyl)amino]-6-(1-piperazinyl)-1,3,5-triazin-2-yl]amino}ethyl)phenol
    参考文献:
    名称:
    Piperazinyltriazines as estrogen receptor modulators
    摘要:
    本文描述了式(I)的三嗪衍生物,其在雌激素受体α(ERα)和β(ERβ)上表现出药理活性。所述发明还包括含有三嗪衍生物的组合物和药物,以及制备和使用这种化合物、组合物和药物的方法。
    公开号:
    US20040072829A1
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文献信息

  • Sulfamide derivatives useful as beta3 agonists and pharmaceutical uses thereof
    申请人:Pfizer Products Inc.
    公开号:EP1236723A1
    公开(公告)日:2002-09-04
    Sulfamide compounds having formula (I) are described as well as their use in the treatment of diseases dependent on the signaling pathways associated with β-adrenergic receptors, such as obesity, diabetes, hypertension, gastrointestinal hypo- or hyper-motility and cardiovascular diseases.
    公式(I)的磺胺化合物被描述,并且它们被用于治疗依赖于与β-肾上腺素受体相关的信号通路的疾病,例如肥胖症、糖尿病、高血压、胃肠道低动力或高动力以及心血管疾病。
  • Beta3 agonists and uses thereof
    申请人:——
    公开号:US20020128247A1
    公开(公告)日:2002-09-12
    Sulfamide compounds having formula (I) are described as well as their use in the treatment of diseases dependent on the signaling pathways associated with &bgr;-adrenergic receptors, such as obesity, diabetes, hypertension, gastrointestinal hypo- or hyper-motility and cardiovascular diseases. 1
    化学式为(I)的磺胺化合物被描述,并且它们在治疗依赖与β-肾上腺素受体相关的信号通路的疾病中的用途也被描述,例如肥胖症、糖尿病、高血压、胃肠道低动力或高动力和心血管疾病。
  • US6939867B2
    申请人:——
    公开号:US6939867B2
    公开(公告)日:2005-09-06
  • US6943162B2
    申请人:——
    公开号:US6943162B2
    公开(公告)日:2005-09-13
  • [EN] PIPERAZINYLTRIAZINES AS ESTROGEN RECEPTOR MODULATORS<br/>[FR] PIPERAZINYLTRIAZINES EN TANT QUE MODULATEURS DE RECEPTEURS D'OESTROGENES
    申请人:SMITHKLINE BEECHAM CORP
    公开号:WO2002072561A1
    公开(公告)日:2002-09-19
    Triazine derivatives of formula (I), which exhibit pharmacological activity at estrogen receptors alpha (ER alpha) and beta (ER beta) are described herein. The described invention also includes compositions and medicaments containing the triazine derivatives as well as processes for the preparation and use of such compounds, compositions and medicaments.
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