(2,5-dioxopyrrolidin-1-yl) N-cycloheptylcarbamate | 1017575-78-8

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 吡咯烷类
• 英文名称: (2,5-dioxopyrrolidin-1-yl) N-cycloheptylcarbamate
• CAS: 1017575-78-8
• 化学式: C₁₂H₁₈N₂O₄
• 分子量: 254.286
• InChiKey: JVGLDLQCDBPIIE-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.4
• 重原子数：
  18
• 可旋转键数：
  3
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.75
• 拓扑面积：
  75.7
• 氢给体数：
  1
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  (2,5-dioxopyrrolidin-1-yl) N-cycloheptylcarbamate 、 (1S,5R)-7-oxo-2,6-diazabicyclo<3.2.0>heptane-6-sulfonic acid 在 水 、 碳酸氢钠 作用下， 以 乙腈 为溶剂， 生成 (1S,5R)-2-(cycloheptylaminocarbonyl)-7-oxo-2,6-diazabicyclo[3.2.0]heptane-6-sulfonic acid
  参考文献：
  名称：

  Side chain SAR of bicyclic β-lactamase inhibitors (BLIs). 1. Discovery of a class C BLI for combination with imipinem

  摘要：

  Bridged monobactam beta-lactamase inhibitors were prepared and evaluated as potential partners for combination with imipenem to overcome class C beta-lactamase mediated resistance. The (S)-azepine analog 2 was found to be effective in both in vitro and in vivo assays and was selected for preclinical development.

  DOI：

  10.1016/j.bmcl.2009.12.069
• 作为产物：
  描述：

  N,N'-二琥珀酰亚胺基碳酸酯 、 环庚胺 以 乙腈 为溶剂， 生成 (2,5-dioxopyrrolidin-1-yl) N-cycloheptylcarbamate
  参考文献：
  名称：

  Side chain SAR of bicyclic β-lactamase inhibitors (BLIs). 1. Discovery of a class C BLI for combination with imipinem

  摘要：

  Bridged monobactam beta-lactamase inhibitors were prepared and evaluated as potential partners for combination with imipenem to overcome class C beta-lactamase mediated resistance. The (S)-azepine analog 2 was found to be effective in both in vitro and in vivo assays and was selected for preclinical development.

  DOI：

  10.1016/j.bmcl.2009.12.069

文献信息

• NOVEL INHIBITORS OF BETA-LACTAMASE
  申请人：Blizzard Timothy A.

  公开号：US20100009957A1

  公开（公告）日：2010-01-14

  A class of 7-oxo-2,6-diazabicyclo-[3.2.0]-heptane-6-sulfonic acid compounds substituted at the two position of the bicyclic ring with a heterocyclylaminocarbonyl group or a carbocyclylaminocarbonyl group are β-lactamase inhibitors. The compounds and their prodrugs and pharmaceutically acceptable salts are useful in the treatment of bacterial infections in combination with β-lactam antibiotics. In particular, the compounds are suitable for use with β-lactam antibiotics (e.g., imipenem and ceftazidime) against micro-organisms resistant to β-lactam antibiotics due to the presence of the β-lactamases.

  一类7-氧代-2,6-二氮杂双环[3.2.0]庚烷-6-磺酸化合物，在双环环上的2位取代了杂环氨基甲酰基团或碳环氨基甲酰基团，是β-内酰胺酶抑制剂。这些化合物及其前药和药学上可接受的盐在联合β-内酰胺类抗生素治疗细菌感染方面非常有用。特别是，这些化合物适用于与β-内酰胺类抗生素（例如亚胺培南和头孢他啶）一起使用，对于由于β-内酰胺酶的存在而对β-内酰胺类抗生素产生耐药性的微生物非常有效。
• [EN] NOVEL INHIBITORS OF BETA-LACTAMASE<br/>[FR] NOUVEAUX INHIBITEURS DE BÊTA-LACTAMASE
  申请人：MERCK & CO INC

  公开号：WO2008039420A2

  公开（公告）日：2008-04-03

  [EN] A class of 7-oxo-2,6-diazabicyclo-[3.2.0]-heptane-6-sulfonic acid compounds substituted at the two position of the bicyclic ring with a heterocyclylaminocarbonyl group or a carbocyclylaminocarbonyl group are ß-lactamase inhibitors. The compounds and their prodrugs and pharmaceutically acceptable salts are useful in the treatment of bacterial infections in combination with ß-lactam antibiotics. In particular, the compounds are suitable for use with ß-lactam antibiotics (e.g., imipenem and ceftazidime) against micro-organisms resistant to ß-lactam antibiotics due to the presence of the ß-lactamases.
  [FR] L'invention concerne une classe de composés d'acide 7-oxo-2,6-diazabicyclo-[3.2.0]-heptane-6-sulfonique, substitués à la position 2 du noyau bicyclique par un groupe hétérocyclylaminocarbonyle ou un groupe carbocyclylaminocarbonyle, qui sont des inhibiteurs de bêta-lactamase. Ces composés, ainsi que leurs promédicaments et leurs sels pharmaceutiquement acceptables, sont utiles dans le traitement d'infections bactériennes lorsqu'ils sont associés à des antibiotiques bêta-lactame (p. ex. imipenem and ceftazidime) pour lutter contre des micro-organismes résistants aux antibiotiques bêta-lactame, du fait de la présence des bêta-lactamases.