2-chloro-1-[3-hydroxy-2-(tetrahydropyran-2-yloxy)propyl]-4-nitroimidazole | 683276-62-2

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 唑类
• 英文名称: 2-chloro-1-[3-hydroxy-2-(tetrahydropyran-2-yloxy)propyl]-4-nitroimidazole
• 英文别名: 3-(2-Chloro-4-nitroimidazol-1-yl)-2-(oxan-2-yloxy)propan-1-ol
• CAS: 683276-62-2
• 化学式: C₁₁H₁₆ClN₃O₅
• 分子量: 305.718
• InChiKey: AEFONMRCCJYAER-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.2
• 重原子数：
  20
• 可旋转键数：
  5
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.73
• 拓扑面积：
  102
• 氢给体数：
  1
• 氢受体数：
  6

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。
• Nitroimidazole Compounds
  申请人：Jiricek Jan

  公开号：US20080275035A1

  公开（公告）日：2008-11-06

  The present invention relates to certain nitroimidazole compounds, which have interesting pharmaceutical properties. In particular, the compounds are useful in the treatment and/or prevention of infections such as those caused by Mycobacterium tuberculosis, Trypanosoma cruzi or Leishmania donovani . The invention also relates to pharmaceutical compositions containing the compounds, as well as processes for their preparation.

  本发明涉及某些硝基咪唑化合物，具有有趣的药理特性。特别地，这些化合物在治疗和/或预防由结核分枝杆菌、克鲁兹锥虫或唇鞭毛虫等引起的感染方面是有用的。该发明还涉及含有这些化合物的药物组合物，以及它们的制备方法。
• 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。