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

4-Hydroxy-1-(3-trifluoromethoxyphenyl)-3-(4-trifluoromethylphenylacetyl)-1,8-naphthyridin-2(1H)-one | 929612-49-7

中文名称
——
中文别名
——
英文名称
4-Hydroxy-1-(3-trifluoromethoxyphenyl)-3-(4-trifluoromethylphenylacetyl)-1,8-naphthyridin-2(1H)-one
英文别名
4-hydroxy-1-(3-trifluoromethoxyphenyl)-3-(4-trifluoromethylphenylacetyl)-1,8-naphthyridine-2(1H)-one;4-hydroxy-1-[3-(trifluoromethoxy)phenyl]-3-[2-[4-(trifluoromethyl)phenyl]acetyl]-1,8-naphthyridin-2-one
4-Hydroxy-1-(3-trifluoromethoxyphenyl)-3-(4-trifluoromethylphenylacetyl)-1,8-naphthyridin-2(1H)-one化学式
CAS
929612-49-7
化学式
C24H14F6N2O4
mdl
——
分子量
508.377
InChiKey
XOXGDXGKWAAJAP-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):
    5.8
  • 重原子数:
    36
  • 可旋转键数:
    5
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.12
  • 拓扑面积:
    79.7
  • 氢给体数:
    1
  • 氢受体数:
    11

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

反应信息

  • 作为反应物:
    描述:
    4-Hydroxy-1-(3-trifluoromethoxyphenyl)-3-(4-trifluoromethylphenylacetyl)-1,8-naphthyridin-2(1H)-one 作用下, 以 N,N-二甲基甲酰胺 为溶剂, 反应 2.0h, 以32%的产率得到5-(3-trifluoromethoxyphenyl)-3-(4-trifluoromethylbenzyl)-1H-pyrazolo[4,3-c][1,8]naphthyridin-4(5H)-one
    参考文献:
    名称:
    HETEROCYCLIC COMPOUND, AND PRODUCTION PROCESS AND USE THEREOF
    摘要:
    公开号:
    EP1925617B1
  • 作为产物:
    描述:
    4-hydroxy-1-(3-trifluoromethoxyphenyl)-1,8-naphthyridin-2(1H)-one 、 2-[4-(三氟甲基)苯基]乙酰氯 在 sodium hydride 作用下, 以 N,N-二甲基甲酰胺 为溶剂, 反应 1.0h, 以42%的产率得到4-Hydroxy-1-(3-trifluoromethoxyphenyl)-3-(4-trifluoromethylphenylacetyl)-1,8-naphthyridin-2(1H)-one
    参考文献:
    名称:
    HETEROCYCLIC COMPOUND, AND PRODUCTION PROCESS AND USE THEREOF
    摘要:
    公开号:
    EP1925617B1
点击查看最新优质反应信息

文献信息

  • Heterocycle compound, and production process and application thereof
    申请人:Aska Pharmaceutical Co., Ltd.
    公开号:US08193356B2
    公开(公告)日:2012-06-05
    The compound of the present invention is a novel compound which has a specific heterocycle skeleton, particularly a pyrazolonaphthyridine or pyrazoloquinoline skeleton having an organic group (e.g., a carbocycle and a heterocycle) bonding through an alkylene group at 3-position and a carbocycle bonding at 5-position and has a phosphodiesterase IV inhibitory activity. At least one of the ring (the carbocycle or the heterocycle) bonding at 3-position of the pyrazolonaphthyridine skeleton and the carbocycle bonding at 5-position may have a halogenated alkyl group and/or a halogenated alkoxy group as a substituent. Such a compound or a salt thereof is useful as a phosphodiesterase IV inhibitor and the like. According to the present invention, a novel compound having a high phosphodiesterase IV inhibitory effect can be provided.
    本发明的化合物是一种具有特定杂环骨架的新型化合物,特别是具有通过3位的烷基与5位的碳环键合的有机基团(例如,碳环和杂环)的吡唑啉萘或吡唑喹啉骨架,并具有磷酸二酯酶IV抑制活性。在吡唑啉萘骨架的3位和5位的碳环键合中,至少一个环(碳环或杂环)可能具有卤代烷基和/或卤代烷氧基作为取代基。这样的化合物或其盐对于磷酸二酯酶IV抑制剂等具有用途。根据本发明,可以提供一种具有高磷酸二酯酶IV抑制效果的新型化合物。
  • Heterocycle Compound, and Production Process and Application Thereof
    申请人:Kanazawa Hashime
    公开号:US20090131467A1
    公开(公告)日:2009-05-21
    The compound of the present invention is a novel compound which has a specific heterocycle skeleton, particularly a pyrazolonaphthyridine or pyrazoloquinoline skeleton having an organic group (e.g., a carbocycle and a heterocycle) bonding through an alkylene group at 3-position and a carbocycle bonding at 5-position and has a phosphodiesterase IV inhibitory activity. At least one of the ring (the carbocycle or the heterocycle) bonding at 3-position of the pyrazolonaphthyridine skeleton and the carbocycle bonding at 5-position may have a halogenated alkyl group and/or a halogenated alkoxy group as a substituent. Such a compound or a salt thereof is useful as a phosphodiesterase IV inhibitor and the like. According to the present invention, a novel compound having a high phosphodiesterase IV inhibitory effect can be provided.
    本发明的化合物是一种新型化合物,具有特定的杂环骨架,特别是具有通过3位的烷基与5位的碳环键合的有机基团(例如,碳环和杂环)的吡唑萘啶或吡唑喹啉骨架,并具有磷酸二酯酶IV抑制活性。在吡唑萘啶骨架的3位键合的环(碳环或杂环)和5位键合的碳环中,至少有一个可以具有卤代烷基和/或卤代烷氧基作为取代基。这种化合物或其盐可用作磷酸二酯酶IV抑制剂等。根据本发明,可以提供一种具有高磷酸二酯酶IV抑制效果的新型化合物。
  • US8193356B2
    申请人:——
    公开号:US8193356B2
    公开(公告)日:2012-06-05
  • HETEROCYCLIC COMPOUND, AND PRODUCTION PROCESS AND USE THEREOF
    申请人:ASKA Pharmaceutical Co., Ltd.
    公开号:EP1925617B1
    公开(公告)日:2012-11-14
查看更多