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6-methoxy-2-methylquinazoline-4-thiol

中文名称
——
中文别名
——
英文名称
6-methoxy-2-methylquinazoline-4-thiol
英文别名
6-methoxy-2-methyl-1H-quinazoline-4-thione
6-methoxy-2-methylquinazoline-4-thiol化学式
CAS
——
化学式
C10H10N2OS
mdl
——
分子量
206.268
InChiKey
NZOIOMLIKSXIDI-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):
    1.3
  • 重原子数:
    14
  • 可旋转键数:
    1
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.2
  • 拓扑面积:
    65.7
  • 氢给体数:
    1
  • 氢受体数:
    2

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:
    N-((5-(2-bromoacetyl)thiophen-2-yl)methyl)-2-hydroxyacetamide 、 6-methoxy-2-methylquinazoline-4-thiolsodium methylate 作用下, 以 N,N-二甲基甲酰胺 为溶剂, 以16.25 g的产率得到2-hydroxy-N-((5-(2-((6-methoxy-2-methylquinazolin-4-yl)thio)acetyl)thiophen-2-yl)methyl)acetamide
    参考文献:
    名称:
    [EN] COMPOUNDS AND USE THEREOF AS HDAC6 INHIBITORS
    [FR] COMPOSÉS ET LEUR UTILISATION COMME INHIBITEURS D'HDAC6
    摘要:
    The present invention relates to a compound of formula (I) or a pharmaceutically acceptable salt and/or solvate thereof, wherein Y1is a 9- or 10-membered bicyclic heteroaryl, Y2is a 5-membered heteroaryl, Z1is selected from (C=O)-R9, S(O)-R9and S(O2)-R9, L is an alkyl-, cycloalkyl- or heterocycloalkyl-based linker, and R1and R9may be various groups. The present invention further relates to a compound of formula (I) as HDAC6 inhibitor, typically for use in the treatment and/or the prevention of an HDAC6-associated disease, such as cancers, neurodegenerative diseases, neuropathies or cardiovascular diseases.
    公开号:
    WO2023118507A2
  • 作为产物:
    描述:
    2-氨基-5-甲氧基苯甲酰胺劳森试剂 、 sodium hydride 作用下, 以 乙醇甲苯 为溶剂, 反应 24.0h, 生成 6-methoxy-2-methylquinazoline-4-thiol
    参考文献:
    名称:
    [EN] COMPOUNDS AND USE THEREOF AS HDAC6 INHIBITORS
    [FR] COMPOSÉS ET LEUR UTILISATION COMME INHIBITEURS D'HDAC6
    摘要:
    The present invention relates to a compound of formula (I) or a pharmaceutically acceptable salt and/or solvate thereof, wherein Y1is a 9- or 10-membered bicyclic heteroaryl, Y2is a 5-membered heteroaryl, Z1is selected from (C=O)-R9, S(O)-R9and S(O2)-R9, L is an alkyl-, cycloalkyl- or heterocycloalkyl-based linker, and R1and R9may be various groups. The present invention further relates to a compound of formula (I) as HDAC6 inhibitor, typically for use in the treatment and/or the prevention of an HDAC6-associated disease, such as cancers, neurodegenerative diseases, neuropathies or cardiovascular diseases.
    公开号:
    WO2023118507A2
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文献信息

  • [EN] COMPOUNDS AND USE THEREOF AS HDAC6 INHIBITORS<br/>[FR] COMPOSÉS ET LEUR UTILISATION COMME INHIBITEURS D'HDAC6
    申请人:[en]AUGUSTINE THERAPEUTICS
    公开号:WO2023118507A2
    公开(公告)日:2023-06-29
    The present invention relates to a compound of formula (I) or a pharmaceutically acceptable salt and/or solvate thereof, wherein Y1is a 9- or 10-membered bicyclic heteroaryl, Y2is a 5-membered heteroaryl, Z1is selected from (C=O)-R9, S(O)-R9and S(O2)-R9, L is an alkyl-, cycloalkyl- or heterocycloalkyl-based linker, and R1and R9may be various groups. The present invention further relates to a compound of formula (I) as HDAC6 inhibitor, typically for use in the treatment and/or the prevention of an HDAC6-associated disease, such as cancers, neurodegenerative diseases, neuropathies or cardiovascular diseases.
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