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3-(Bromomethyl)-6,6-difluorobicyclo[3.1.0]hexane | 1393569-74-8

中文名称
——
中文别名
——
英文名称
3-(Bromomethyl)-6,6-difluorobicyclo[3.1.0]hexane
英文别名
——
3-(Bromomethyl)-6,6-difluorobicyclo[3.1.0]hexane化学式
CAS
1393569-74-8
化学式
C7H9BrF2
mdl
——
分子量
211.05
InChiKey
HVJUHLMGAMROFL-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):
    2.7
  • 重原子数:
    10
  • 可旋转键数:
    1
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    0
  • 氢给体数:
    0
  • 氢受体数:
    2

文献信息

  • HETEROCYCLIC P2X7 ANTAGONISTS
    申请人:AXXAM S.p.A.
    公开号:EP3619200A1
    公开(公告)日:2020-03-11
  • [EN] HETEROCYCLIC P2X7 ANTAGONISTS<br/>[FR] ANTAGONISTES HÉTÉROCYCLIQUES DE P2X7
    申请人:AXXAM SPA
    公开号:WO2018202694A1
    公开(公告)日:2018-11-08
    The present invention refers to compounds of the following formula (I) or a pharmaceutically acceptable salt thereof, to pharmaceutical compositions containing them and to a process for the preparation of said compounds: Formula (I), wherein: R1 is independently selected from hydrogen atom, amine group, monocyclic or bicyclic aliphatic, aromatic, heteroaliphatic or heteroaromatic ring, optionally substituted by one or more substituents selected from C1-C4 alkyl optionally substituted by one or more halogen atom(s), halogen, C1-C4 alkoxy or phenyl group, optionally substituted by C1-C4 alkyl; R2 is independently selected from monocyclic or bicylic aliphatic, heteroaliphatic, aromatic or heteroaromatic ring, C1-C6 alkyl, alkenyl or alkynyl chain, optionally substituted by one or more substituents selected from C1-C4 alkyl optionally substituted by one or more halogen atom(s), halogen, C1-C4 alkoxy, cyano, C1-C4 alkylthio, SO-C1-C4 alkyl, SO2-C1-C4 alkyl, N(C1-C4 alkyl)2; n is 1 or 2; preferably n is 1; m is 0, 1 or 2; preferably m is 0; R3 and R4 can be, independently, -H, -F, C1-C4 alkyl, -OH, -OC1-C4 alkyl; preferably they are both -H; X is O or S; R5 is -H or -CH3 optionally substituted by one or more fluorine atoms; preferably R5 is hydrogen. The compounds of the invention can be used in the treatment of conditions or diseases mediated by P2X7 receptor.
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