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3-氨基-6-氯-5-氟吡啶 | 1256806-83-3

中文名称
3-氨基-6-氯-5-氟吡啶
中文别名
6-氯-5-氟吡啶-3-胺
英文名称
6-Chloro-5-fluoropyridin-3-amine
英文别名
——
3-氨基-6-氯-5-氟吡啶化学式
CAS
1256806-83-3
化学式
C5H4ClFN2
mdl
MFCD18257897
分子量
146.55
InChiKey
HAZMBQGWYYGRES-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:
    283.0±35.0 °C(Predicted)
  • 密度:
    1.449±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    1.2
  • 重原子数:
    9
  • 可旋转键数:
    0
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    38.9
  • 氢给体数:
    1
  • 氢受体数:
    3

安全信息

  • 危险性防范说明:
    P261,P305+P351+P338
  • 危险性描述:
    H302,H315,H319,H335

文献信息

  • PYRIDONE DERIVATIVE HAVING TETRAHYDROPYRANYLMETHYL GROUP
    申请人:DAIICHI SANKYO COMPANY, LIMITED
    公开号:US20170183329A1
    公开(公告)日:2017-06-29
    The present disclosure provides novel compounds or salts thereof, or crystals of the compounds or the salts, which inhibit Axl and are useful in the treatment of a disease caused by hyperfunction of Axl, the treatment of a disease associated with hyperfunction of Axl, and/or the treatment of a disease involving hyperfunction of Axl. The present disclosure provides pyridone derivatives having a tetrahydropyranylmethyl group represented by the following formula (I) having various substituents, or salts thereof, or crystals of the compounds or the salts, wherein R 1 , R 2 , R 3 , R 4 , R 5 , W, X, Y, and Z are each as defined in the specification:
    本公开提供了新颖的化合物或其盐,或者该化合物或盐的晶体,其抑制Axl并在治疗由Axl高功能引起的疾病、与Axl高功能相关的疾病的治疗和/或涉及Axl高功能的疾病的治疗中有用。本公开提供了具有以下式(I)所代表的四氢吡喃基甲基基团的吡啶酮衍生物,具有各种取代基,或其盐,或化合物或盐的晶体,其中R1、R2、R3、R4、R5、W、X、Y和Z均如规范中定义的。
  • PYRIDONE DERIVATIVE HAVING TETRAHYDROPYRANYL METHYL GROUP
    申请人:Daiichi Sankyo Company, Limited
    公开号:EP3168219A1
    公开(公告)日:2017-05-17
    It is intended to provide a novel compound or a salt thereof, or crystals of the compound or the salt, which inhibit Axl and are useful in the treatment of a disease caused by hyperfunction of Axl, the treatment of a disease associated with hyperfunction of Axl, and/or the treatment of a disease involving hyperfunction of Axl. [Solution] The present invention provides a pyridone derivative having a tetrahydropyranylmethyl group represented by the following formula (I) having various substituents, or a salt thereof, or crystals of the compound or the salt (wherein R1, R2, R3, R4, R5, W, X, Y, and Z are each as defined in the specification).
    本发明旨在提供一种新型化合物或其盐,或该化合物或其盐的结晶,该化合物或其盐可抑制 Axl,并可用于治疗由 Axl 功能亢进引起的疾病、治疗与 Axl 功能亢进相关的疾病和/或治疗涉及 Axl 功能亢进的疾病。 [解决方案] 本发明提供一种吡啶酮衍生物,该衍生物具有下式(I)所代表的具有各种取代基的四氢吡喃甲基,或其盐,或该化合物或该盐的结晶(其中R1、R2、R3、R4、R5、W、X、Y和Z各自如说明书中所定义)。
  • Pyridone derivatives having tetrahydropyranylmethyl groups
    申请人:DAIICHI SANKYO COMPANY, LIMITED
    公开号:US10442797B2
    公开(公告)日:2019-10-15
    The present disclosure provides novel compounds or salts thereof, or crystals of the compounds or the salts, which inhibit Axl and are useful in the treatment of a disease caused by hyperfunction of Axl, the treatment of a disease associated with hyperfunction of Axl, and/or the treatment of a disease involving hyperfunction of Axl. The present disclosure provides pyridone derivatives having a tetrahydropyranylmethyl group represented by the following formula (I) having various substituents, or salts thereof, or crystals of the compounds or the salts, wherein R1, R2, R3, R4, R5, W, X, Y, and Z are each as defined in the specification:
    本公开提供了新型化合物或其盐,或化合物或其盐的结晶,它们抑制Axl,可用于治疗由Axl功能亢进引起的疾病、治疗与Axl功能亢进相关的疾病和/或治疗涉及Axl功能亢进的疾病。 本公开提供了具有下式(I)所代表的具有各种取代基的四氢吡喃甲基的吡啶酮衍生物,或其盐,或化合物或其盐的结晶,其中R1、R2、R3、R4、R5、W、X、Y和Z各自如说明书中所定义:
  • Pyrazole derivatives as MALT1 inhibitors
    申请人:Janssen Pharmaceutica NV
    公开号:US10888550B2
    公开(公告)日:2021-01-12
    Disclosed are compounds, compositions and methods for treating of diseases, syndromes, conditions, and disorders that are affected by the modulation of MALT1. Such compounds are represented by Formula (I) as follows: wherein R1, R2, R3, R4, R5, R6, R7, G1 and G2, are defined herein.
    本发明公开了用于治疗受 MALT1 调节影响的疾病、综合征、病症和失调的化合物、组合物和方法。 此类化合物由如下式 (I) 表示:其中 R1、R2、R3、R4、R5、R6、R7、G1 和 G2 在此定义。
  • N-SUBSTITUTED HETERO-BICYCLIC COMPOUNDS AND DERIVATIVES FOR COMBATING ANIMAL PESTS
    申请人:BASF SE
    公开号:EP2694507B1
    公开(公告)日:2017-03-01
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