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3-(4-trifluoromethylphenyl)-2-propenyl (S)-4-{3-[4-nitro-2-(2-nitrophenylthio)imidazol-1-yl]-2-hydroxy-2-methylpropyl}piperazin-1-carboxylate | 683276-75-7

中文名称
——
中文别名
——
英文名称
3-(4-trifluoromethylphenyl)-2-propenyl (S)-4-{3-[4-nitro-2-(2-nitrophenylthio)imidazol-1-yl]-2-hydroxy-2-methylpropyl}piperazin-1-carboxylate
英文别名
3-(4-Trifluoromethylphenyl)-2-propenyl(s)-4-{3-[4-nitro-2-(2-nitrophenylthio)imidazol-1-yl]-2-hydroxy-2-methylpropyl}piperazin-1-carboxylate;3-[4-(trifluoromethyl)phenyl]prop-2-enyl 4-[(2S)-2-hydroxy-2-methyl-3-[4-nitro-2-(2-nitrophenyl)sulfanylimidazol-1-yl]propyl]piperazine-1-carboxylate
3-(4-trifluoromethylphenyl)-2-propenyl (S)-4-{3-[4-nitro-2-(2-nitrophenylthio)imidazol-1-yl]-2-hydroxy-2-methylpropyl}piperazin-1-carboxylate化学式
CAS
683276-75-7
化学式
C28H29F3N6O7S
mdl
——
分子量
650.635
InChiKey
XJNOHGVIWYKJEL-MHZLTWQESA-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):
    4.6
  • 重原子数:
    45
  • 可旋转键数:
    10
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.36
  • 拓扑面积:
    188
  • 氢给体数:
    1
  • 氢受体数:
    13

反应信息

点击查看最新优质反应信息

文献信息

  • 1-substituted-4-nitroimidazole compound and process for producing the same
    申请人:Goto Fumitake
    公开号:US20060079697A1
    公开(公告)日:2006-04-13
    The present invention relates to a 1-substituted-4-nitroimidazole compound represented by the general formula (1) or a salt thereof, (wherein R is a hydrogen atom, a lower alkoxy group-substituted lower alkyl group, a phenyl-lower alkoxy group-substituted lower alkyl group, a cyano-substituted lower alkyl group, a phenyl-lower alkyl group which may have lower alkoxy groups as the substituents in the phenyl ring or a group of the formula —CH 2 R A ; X is a halogen atom or a group of the formula —S(O)n—R 1 ) and method for preparing the same. The compound of the formula (1) is a useful compound as an intermediate for synthesis of various pharmaceutical and agricultural chemicals, particularly, as intermediates for antitubercular agents.
    本发明涉及一种1-取代-4-硝基咪唑化合物,其通式为(1),或其盐,其中R是氢原子,低烷氧基取代的低烷基,苯基-低烷氧基取代的低烷基,氰基取代的低烷基,苯基-低烷基(苯环上可能有低烷氧基取代物)或式子-CH2RA的基团;X是卤素原子或式子-S(O)n-R1的基团。本发明还涉及其制备方法。式(1)的化合物是一种有用的化合物,可用作合成各种药物和农药化学品的中间体,特别是抗结核药物的中间体。
  • 1-Substituted-4-nitroimidazole compound and method for preparing the same
    申请人:Goto Fumitaka
    公开号:US20080200689A1
    公开(公告)日:2008-08-21
    The present invention relates to a 1-substituted-4-nitroimidazole compound represented by the general formula (1) or a salt thereof, (wherein R is a hydrogen atom, a lower alkoxy group-substituted lower alkyl group, a phenyl-lower alkoxy group-substituted lower alkyl group, a cyano-substituted lower alkyl group, a phenyl-lower alkyl group which may have lower alkoxy groups as the substituents in the phenyl ring or a group of the formula —CH 2 R A ; X is a halogen atom or a group of the formula —S(O)n-R 1 ) and method for preparing the same. The compound of the formula (1) is a useful compound as an intermediate for synthesis of various pharmaceutical and agricultural chemicals, particularly, as intermediates for antitubercular agents.
    本发明涉及一种由通式(1)表示的1-取代-4-硝基咪唑化合物或其盐(其中R是氢原子、较低烷氧基取代的较低烷基、苯基-较低烷氧基取代的较低烷基、氰基取代的较低烷基、苯基-较低烷基(苯环上可能存在较低烷氧基作为取代基)或式子—CH2RA的基团;X是卤素原子或式子—S(O)n-R1的基团),以及其制备方法。通式(1)的化合物是一种有用的化合物,可用作合成各种药物和农药化学品的中间体,特别是用作抗结核药物的中间体。
  • 1-substituted-4-nitroimidazole compound and method for preparing the same
    申请人:Goto Fumitaka
    公开号:US20080097107A1
    公开(公告)日:2008-04-24
    The present invention relates to a 1-substituted-4-nitroimidazole compound represented by the general formula (1) or a salt thereof, (wherein R is a hydrogen atom, a lower alkoxy group-substituted lower alkyl group, a phenyl-lower alkoxy group-substituted lower alkyl group, a cyano-substituted lower alkyl group, a phenyl-lower alkyl group which may have lower alkoxy groups as the substituents in the phenyl ring or a group of the formula —CH 2 R A ; X is a halogen atom or a group of the formula —S(O)n-R 1 ) and method for preparing the same. The compound of the formula (1) is a useful compound as an intermediate for synthesis of various pharmaceutical and agricultural chemicals, particularly, as intermediates for antitubercular agents.
    本发明涉及一种由通式(1)表示的1-取代-4-硝基咪唑化合物或其盐,其中R是氢原子、低位烷氧基取代的低碳基、苯基-低位烷氧基取代的低碳基、氰基取代的低碳基、苯基-低碳基(苯环上可能有低位烷氧基取代物)或公式-CH2RA的基团;X是卤素原子或公式-S(O)n-R1的基团。本发明还涉及制备该化合物的方法。式(1)的化合物是一种有用的化合物,可用作合成各种制药和农业化学品的中间体,特别是抗结核药物的中间体。
  • 1-Substituted-4-Nitroimidazole Compound and Method for Preparing the Same
    申请人:GOTO Fumitaka
    公开号:US20120130082A1
    公开(公告)日:2012-05-24
    The present invention relates to a 1-substituted-4-nitroimidazole compound represented by the general formula (1) or a salt thereof, (wherein R is a hydrogen atom, a lower alkoxy group-substituted lower alkyl group, a phenyl-lower alkoxy group-substituted lower alkyl group, a cyano-substituted lower alkyl group, a phenyl-lower alkyl group which may have lower alkoxy groups as the substituents in the phenyl ring or a group of the formula —CH 2 R A ; X is a halogen atom or a group of the formula —S(O)n-R 1 ) and method for preparing the same. The compound of the formula (1) is a useful compound as an intermediate for synthesis of various pharmaceutical and agricultural chemicals, particularly, as intermediates for antitubercular agents.
    本发明涉及一种由通式(1)表示的1-取代-4-硝基咪唑化合物或其盐(其中R为氢原子,低烷氧基取代的低烷基,苯基-低烷氧基取代的低烷基,氰基取代的低烷基,苯基-低烷基,其苯环上可能带有低烷氧基取代物,或者为公式—CH2RA的基团;X为卤素原子或公式—S(O)n-R1的基团),以及制备该化合物的方法。公式(1)的化合物是一种有用的中间体,可用于合成各种医药和农业化学品,特别是抗结核药物的中间体。
  • EP1553088
    申请人:——
    公开号:——
    公开(公告)日:——
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