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methyl 6-chloro-2-hydroxy-3,4-dihydro-1-naphthoate | 869699-73-0

中文名称
——
中文别名
——
英文名称
methyl 6-chloro-2-hydroxy-3,4-dihydro-1-naphthoate
英文别名
methyl 6-chloro-2-hydroxy-3,4-dihydronaphthalene-1-carboxylate
methyl 6-chloro-2-hydroxy-3,4-dihydro-1-naphthoate化学式
CAS
869699-73-0
化学式
C12H11ClO3
mdl
——
分子量
238.671
InChiKey
NSJIORQBJFYKRU-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):
    3.1
  • 重原子数:
    16
  • 可旋转键数:
    2
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.25
  • 拓扑面积:
    46.5
  • 氢给体数:
    1
  • 氢受体数:
    3

反应信息

  • 作为反应物:
    描述:
    methyl 6-chloro-2-hydroxy-3,4-dihydro-1-naphthoate吡啶sodium hydroxideN-溴代丁二酰亚胺(NBS)sodium ethanolate 作用下, 以 乙醇 为溶剂, 反应 34.5h, 生成 3-Amino-8-chlorobenzo(f)quinazolin-1(2H)-one
    参考文献:
    名称:
    Benzoquinazoline inhibitors of thymidylate synthase: enzyme inhibitory activity and cytotoxicity of some 3-amino- and 3-methylbenzo[f]quinazolin-1(2H)-ones
    摘要:
    The synthesis and thymidylate synthase (TS) inhibitory activity of a series of simple benzo-[f]-quinazolin-1(2H)-ones are described. Fully aromatic 3-amino compounds with compact lipophilic substituents in the 9-position were found to have I50 values as low as 20 nM on the isolated enzyme, and represent the first examples of potent, folate-based TS inhibitors that completely lack any structural feature corresponding to the (p-aminobenzoyl)glutamate moiety of the cofactor. A number of the compounds also showed moderate growth inhibitory activity against a human colon adenocarcinoma cell line (SW480), with IC50 values as low as 2 muM.
    DOI:
    10.1021/jm00068a004
  • 作为产物:
    描述:
    6-氯-3,4-二氢-2(1H)-萘酮 在 sodium hydride 、 溶剂黄146 作用下, 以 甲苯 为溶剂, 反应 25.0h, 生成 methyl 6-chloro-2-hydroxy-3,4-dihydro-1-naphthoate
    参考文献:
    名称:
    2H-or 3H-benzo[e]indazol-1-yl carbamate derivatives, the preparation and therapeutic use thereof
    摘要:
    与披露中定义的公式(I)相对应的化合物,制备这种化合物的方法,用于这种方法的中间体,含有本发明化合物的药物组合物,以及使用它们的治疗方法。
    公开号:
    US20070105932A1
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文献信息

  • 2H OR 3H-BENZO[E]INDAZOL-1-YL CARBAMATE DERIVATIVES, THE PREPARATION AND THERAPEUTIC USE THEREOF
    申请人:DUBOIS Laurent
    公开号:US20120108584A1
    公开(公告)日:2012-05-03
    Compounds corresponding to the formula (I) as defined in the disclosure, as well as methods for making such compounds, intermediates employed in such methods, pharmaceutical compositions containing the compounds of the invention, and methods of treatment using them.
    本发明涉及与式(I)相对应的化合物,以及制备这些化合物的方法,用于这些方法的中间体,含有本发明化合物的药物组合物,以及使用它们的治疗方法。
  • 2H- or 3H-benzo[e]indazol-1-yl carbamate derivatives, the preparation and therapeutic use thereof
    申请人:Sanofi-Aventis
    公开号:US08114899B2
    公开(公告)日:2012-02-14
    Compounds corresponding to the formula (I) as defined in the disclosure, as well as methods for making such compounds, intermediates employed in such methods, pharmaceutical compositions containing the compounds of the invention, and methods of treatment using them.
    本发明涉及与公式(I)对应的化合物,以及制备这些化合物的方法,用于这些方法的中间体,含有本发明化合物的药物组合物,以及使用它们的治疗方法。
  • 2H -or 3H-benzo[e]indazol-1-yl carbamate derivatives, the preparation and therapeutic use thereof
    申请人:Sanofi-Aventis
    公开号:US07501449B2
    公开(公告)日:2009-03-10
    Compounds corresponding to the formula (I) as defined in the disclosure as well as methods for making such compounds, intermediates employed in such methods, pharmaceutical compositions containing the compounds of the invention, and methods of treatment using them.
    本发明涉及符合公式(I)的化合物,以及制备这些化合物的方法,用于这些方法的中间体,包含本发明化合物的制药组合物,以及使用它们的治疗方法。
  • 2H or 3H-benzo[E]indazol-1-YL carbamate derivatives, the preparation and therapeutic use thereof
    申请人:Sanofi
    公开号:US08258168B2
    公开(公告)日:2012-09-04
    Compounds corresponding to the formula (I) as defined in the disclosure, as well as methods for making such compounds, intermediates employed in such methods, pharmaceutical compositions containing the compounds of the invention, and methods of treatment using them.
    本发明涉及与公式(I)相对应的化合物,以及制备这些化合物的方法,用于这些方法的中间体,含有本发明化合物的药物组合物,以及使用它们的治疗方法。
  • 2H- OR 3H-BENZO[E]INDAZOL-1-YL CARBAMATE DERIVATIVES, THE PREPARATION AND THERAPEUTIC USE THEREOF
    申请人:DUBOIS Laurent
    公开号:US20090143380A1
    公开(公告)日:2009-06-04
    Compounds corresponding to the formula (I) as defined in the disclosure, as well as methods for making such compounds, intermediates employed in such methods, pharmaceutical compositions containing the compounds of the invention, and methods of treatment using them.
    本发明涉及与公式(I)相对应的化合物,以及制备这种化合物的方法,用于这种方法的中间体,含有本发明化合物的药物组合物,以及使用它们的治疗方法。
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