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4-mercapto-2-phenyl-pyrimidine-5-carboxylic acid (2-diethylamino-ethyl)-amide | 186130-56-3

中文名称
——
中文别名
——
英文名称
4-mercapto-2-phenyl-pyrimidine-5-carboxylic acid (2-diethylamino-ethyl)-amide
英文别名
N-[2-(diethylamino)ethyl]-2-phenyl-6-sulfanylidene-1H-pyrimidine-5-carboxamide
4-mercapto-2-phenyl-pyrimidine-5-carboxylic acid (2-diethylamino-ethyl)-amide化学式
CAS
186130-56-3
化学式
C17H22N4OS
mdl
——
分子量
330.454
InChiKey
GOLRICUZMHEUDD-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):
    1.8
  • 重原子数:
    23
  • 可旋转键数:
    7
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.35
  • 拓扑面积:
    88.8
  • 氢给体数:
    2
  • 氢受体数:
    4

反应信息

  • 作为反应物:
    描述:
    4-mercapto-2-phenyl-pyrimidine-5-carboxylic acid (2-diethylamino-ethyl)-amide 以to give 2.25 g of the title compound的产率得到2-[2-(Diethylamino)ethyl]-6-phenyl-isothiazolo[5,4-d] pyrimidin-3(2H)-one
    参考文献:
    名称:
    Isothiazolones
    摘要:
    异噻唑酮具有一般结构##STR1##其中A是单环或双环环,可能包含最多3个从O、S和N中选择的杂原子;R.sup.1和R.sup.2是取代基,例如烷基、烷氧基、羟基、硝基、氰基、氨基和羧基;而R.sup.5是烷基、环烷基、苯基和Het。异噻唑酮可用作抗逆转录病毒药物、抗炎药物和抗动脉粥样硬化药物。
    公开号:
    US05889034A1
  • 作为产物:
    描述:
    4-chloro-2-phenyl-pyrimidine-5-carboxylic acid (2-diethylamino-ethyl)-amide 、 Sodium hydrogen sulphide 以to afford 4.2 g of the title compound, mp 178°-180° C.的产率得到4-mercapto-2-phenyl-pyrimidine-5-carboxylic acid (2-diethylamino-ethyl)-amide
    参考文献:
    名称:
    Isothiazolone compounds
    摘要:
    异噻唑啉具有一般结构##STR1## 其中A是单环或双环环,可能包含最多3个从O、S和N中选择的杂原子;R.sup.1和R.sup.2是取代基,例如烷基,烷氧基,羟基,硝基,氰基,氨基和羧基;而R.sup.5是烷基,环烷基,苯基和Het。异噻唑啉可用作抗逆转录病毒剂,抗炎剂和抗动脉粥样硬化剂。
    公开号:
    US05733921A1
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文献信息

  • Isothiazolones
    申请人:Warner-Lambert Company
    公开号:US05620997A1
    公开(公告)日:1997-04-15
    Isothiazolones having the general structure ##STR1## where A is a monocyclic or bicyclic ring which may contain up to 3 heteroatoms selected from O, S, and N; R.sup.1 and R.sup.2 are substituent groups such as alkyl, alkoxy, hydroxy, nitro, cyano, amino, and carboxy; and R.sup.5 is alkyl, cycloalkyl, phenyl, and Het. The isothiazolones are useful as anti-retroviral agents, anti-inflammatory agents, and anti-atherosclerotic agents.
    异噻唑酮具有一般结构##STR1##其中A是单环或双环环,可包含最多3个来自O、S和N的杂原子;R.sup.1和R.sup.2是取代基,例如烷基、烷氧基、羟基、硝基、氰基、氨基和羧基;而R.sup.5是烷基、环烷基、苯基和Het。异噻唑酮可用作抗逆转录病毒药物、抗炎药物和抗动脉粥样硬化药物。
  • Isothiazolones lower plasma levels of lipoprotein(a)
    申请人:——
    公开号:US05668162A1
    公开(公告)日:1997-09-16
    Plasma levels of Lp(a) are lowered by administering an isothiazolone having the general structure ##STR1## where A is a monocyclic or bicyclic ring which may contain up to 3 heteroatoms selected from O, S, and N; R.sup.1 and R.sup.2 are substituent groups such as alkyl, alkoxy, hydroxy, nitro, cyano, amino, and carboxy; and R.sup.5 is alkyl, cycloalkyl, phenyl, and Het.
    通过给予具有一般结构##STR1##的异噻唑啉,可以降低Lp(a)的血浆水平,其中A是可以包含最多3个来自O,S和N的杂原子的单环或双环环;R.sup.1和R.sup.2是取代基,例如烷基,烷氧基,羟基,硝基,氰基,氨基和羧基;R.sup.5是烷基,环烷基,苯基和Het。
  • Isothiazolone compounds
    申请人:Warner-Lambert Company
    公开号:US05733921A1
    公开(公告)日:1998-03-31
    Isothiazolones having the general structure ##STR1## where A is a monocyclic or bicyclic ring which may contain up to 3 heteroatoms selected from O, S, and N; R.sup.1 and R.sup.2 are substituent groups such as alkyl, alkoxy, hydroxy, nitro, cyano, amino, and carboxy; and R.sup.5 is alkyl, cycloalkyl, phenyl, and Het. The isothiazolones are useful as anti-retroviral agents, anti-inflammatory agents, and anti-atherosclerotic agents.
    异噻唑啉具有一般结构##STR1## 其中A是单环或双环环,可能包含最多3个从O、S和N中选择的杂原子;R.sup.1和R.sup.2是取代基,例如烷基,烷氧基,羟基,硝基,氰基,氨基和羧基;而R.sup.5是烷基,环烷基,苯基和Het。异噻唑啉可用作抗逆转录病毒剂,抗炎剂和抗动脉粥样硬化剂。
  • Isothiazolones and pharmaceutical formulations
    申请人:Warner-Lambert Company
    公开号:US06133270A1
    公开(公告)日:2000-10-17
    Isothiazolones having the general structure ##STR1## where A is a monocyclic or bicyclic ring which may contain up to 3 heteroatoms selected from O, S, and N; R.sup.1 and R.sup.2 are substituent groups such as alkyl, alkoxy, hydroxy, nitro, cyano, amino, and carboxy; and R.sup.5 is alkyl, cycloalkyl, phenyl, and Het. The isothiazolones are useful as anti-retroviral agents, anti-inflammatory agents, and anti-atherosclerotic agents.
    Isothiazolones具有一般结构##STR1##其中A是单环或双环,可以含有最多3个来自O,S和N的杂原子;R.sup.1和R.sup.2是取代基,例如烷基,烷氧基,羟基,硝基,氰基,氨基和羧基;而R.sup.5是烷基,环烷基,苯基和Het。Isothiazolones可用作抗逆转录病毒药物,抗炎药物和抗动脉粥样硬化药物。
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