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4-(Methylthio)pyridin-2(1H)-one | 1018443-25-8

中文名称
——
中文别名
——
英文名称
4-(Methylthio)pyridin-2(1H)-one
英文别名
4-methylsulfanyl-1H-pyridin-2-one
4-(Methylthio)pyridin-2(1H)-one化学式
CAS
1018443-25-8
化学式
C6H7NOS
mdl
MFCD19220863
分子量
141.194
InChiKey
VISHERBQTUKZQB-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):
    0.4
  • 重原子数:
    9
  • 可旋转键数:
    1
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.166
  • 拓扑面积:
    54.4
  • 氢给体数:
    1
  • 氢受体数:
    2

反应信息

  • 作为反应物:
    描述:
    4-(Methylthio)pyridin-2(1H)-one 、 (R)-1-(5-iodo-pyridin-2-yl)-pyrrolidin-3-ol 生成 6'-[(3R)-3-hydroxypyrrolidin-1-yl]-4-(methylthio)-2H-1,3'-bipyridin-2-one
    参考文献:
    名称:
    Melanin Concentrating Hormone Receptor-1 Antagonist Pyridinones
    摘要:
    本发明提供了公式(I)的MCHR1拮抗剂化合物及其药学上可接受的盐、溶剂合物和前药,其中取代基如本文所定义,以及其药学上可接受的盐、溶剂合物和前药,其用于治疗拮抗MCHR1受体有益的疾病或病况。
    公开号:
    US20080085884A1
  • 作为产物:
    描述:
    2-氯-4-甲硫基吡啶盐酸 作用下, 反应 1.0h, 生成 4-(Methylthio)pyridin-2(1H)-one
    参考文献:
    名称:
    [EN] GLUCOKINASE ACTIVATORS
    [FR] ACTIVATEURS DE GLUCOKINASE
    摘要:
    公开号:
    WO2008079787A8
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文献信息

  • [EN] SUBSTITUTED 3-AMINO-THIENO[2,3-b]PYRIDINE-2-CARBOXYLIC ACID AMIDE COMPOUNDS AND PROCESSES FOR PREPARING AND THEIR USES<br/>[FR] COMPOSES AMIDE D'ACIDE 3-AMINO-THIENO[2,3-b]PYRIDINE-2-CARBOXYLIQUE SUBSTITUES ET PROCESSUS DE PREPARATION ET D'UTILISATION DE CES COMPOSES
    申请人:BOEHRINGER INGELHEIM PHARMA
    公开号:WO2003103661A1
    公开(公告)日:2003-12-18
    Disclosed are compounds of formula (I), wherein R1 and R2 are defined herein, which are useful as inhibitors of the kinase activity of the IκB kinase (IKK) complex. The compounds are therefore useful in the treatment of IKK mediated diseases including autoimmune diseases inflammatory diseases and cancer. Also disclosed are pharmaceutical compositions comprising these compounds and processes for preparing these compounds.
    公开的是式(I)的化合物,其中R1和R2如本文所定义,这些化合物可用作IκB激酶(IKK)复合物激酶活性的抑制剂。因此,这些化合物在治疗IKK介导的疾病,包括自身免疫疾病、炎症性疾病和癌症方面是有用的。还公开了包含这些化合物的药物组合物以及制备这些化合物的方法。
  • Substituted 3-amino-thieno[2,3-b]pyridine-2-carboxylic acid amide compounds and processes for preparing and their uses
    申请人:Cywin L. Charles
    公开号:US20050288285A1
    公开(公告)日:2005-12-29
    Disclosed are compounds of formula (I): wherein R 1 and R 2 are defined herein, which are useful as inhibitors of the kinase activity of the IκB kinase (IKK) complex. The compounds are therefore useful in the treatment of IKK mediated diseases including autoimmune diseases inflammatory diseases and cancer. Also disclosed are pharmaceutical compositions comprising these compounds and processes for preparing these compounds.
    本发明涉及化合物(I)的公开,其中R1和R2在此定义,这些化合物可用作IκB激酶(IKK)复合物的激酶活性抑制剂。因此,这些化合物可用于治疗由IKK介导的疾病,包括自身免疫性疾病、炎症性疾病和癌症。还公开了包含这些化合物的药物组合物和制备这些化合物的过程。
  • Substituted 3-amino-thieno [2,3-b]pyridine-2-carboxylic acid amide compounds and processes for preparing and their uses
    申请人:Boehringer Ingelheim Pharmaceuticals, Inc.
    公开号:US20040053957A1
    公开(公告)日:2004-03-18
    Disclosed are compounds of formula (I): 1 wherein R 1 and R 2 are defined herein, which are useful as inhibitors of the kinase activity of the I&kgr;B kinase (IKK) complex. The compounds are therefore useful in the treatment of IKK mediated diseases including autoimmune diseases inflammatory diseases and cancer. Also disclosed are pharmaceutical compositions comprising these compounds and processes for preparing these compounds.
    本发明公开了式(I)的化合物:其中R1和R2在此定义,这些化合物可用作IκB激酶(IKK)复合物的激酶活性抑制剂。因此,这些化合物可用于治疗IKK介导的疾病,包括自身免疫性疾病、炎症性疾病和癌症。本发明还公开了包含这些化合物的制药组合物和制备这些化合物的过程。
  • 3-amino-thieno[2,3-b]pyridine-2-carboxylic acid amides
    申请人:Boehringer Ingelheim Pharmaceuticals, Inc.
    公开号:EP2008654A1
    公开(公告)日:2008-12-31
    Disclosed are compounds of formula (I): wherein R1 and R2 are defined herein, which are useful as inhibitors of the kinase activity of the IκB kinase (IKK) complex. The compounds are therefore useful in the treatment of IKK mediated diseases including autoimmune diseases inflammatory diseases and cancer. Also disclosed are pharmaceutical compositions comprising these compounds and processes for preparing these compounds.
    所公开的是式 (I) 化合物: 其中 R1 和 R2 在此定义,可用作 IκB 激酶(IKK)复合物激酶活性的抑制剂。因此,这些化合物可用于治疗 IKK 介导的疾病,包括自身免疫性疾病、炎症性疾病和癌症。此外,还公开了包含这些化合物的药物组合物以及制备这些化合物的工艺。
  • SUBSTITUTED 3-AMINO-THIENO(2,3-b) PYRIDINE-2-CARBOXYLIC ACID AMIDE COMPOUNDS ANDPROCESSES FOR PREPARING AND THEIR USES
    申请人:BOEHRINGER INGELHEIM PHARMACEUTICALS INC.
    公开号:EP1513516A1
    公开(公告)日:2005-03-16
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