2-propanone-1,3-di-t-butyldicarbonate | 625390-30-9

• 分子结构分类: 有机化合物 - 有机酸及其衍生物 - 有机碳酸及其衍生物
• 英文名称: 2-propanone-1,3-di-t-butyldicarbonate
• 英文别名: 3-propanone-1,3-di-t-butyldicarbonate；t-BuOC(O)OCH2C(O)CH2OC(O)OtBu
• CAS: 625390-30-9
• 化学式: C₁₃H₂₂O₇
• 分子量: 290.313
• InChiKey: HKQLIFSHGQLODA-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.46
• 重原子数：
  20.0
• 可旋转键数：
  4.0
• 环数：
  0.0
• sp3杂化的碳原子比例：
  0.77
• 拓扑面积：
  88.13
• 氢给体数：
  0.0
• 氢受体数：
  7.0

反应信息

• 作为反应物：
  描述：

  2-propanone-1,3-di-t-butyldicarbonate 、 三苯基苄基溴化膦 在 正丁基锂 作用下， 以 四氢呋喃 、 正己烷 为溶剂， 反应 16.0h， 以70%的产率得到
  参考文献：
  名称：

  [EN] 6-11 BICYCLIC KETOLIDE DRIVATIVES
  [FR] DERIVES DE KETOLIDE 6-11 BICYCLIQUES

  摘要：

  本发明公开了具有以下结构的化合物I，或其药学上可接受的盐、酯或前药：Formule (I)，其具有抗菌性能。本发明还涉及包括上述化合物的药物组合物，用于给需要抗生素治疗的受试者使用。该发明还涉及通过给予包含本发明化合物的药物组合物来治疗受试者的细菌感染的方法。该发明还包括制备本发明化合物的方法。

  公开号：

  WO2005061526A1
• 作为产物：
  描述：

  二碳酸二叔丁酯 、 dihydroxyacetone dimer 在 吡啶 、 4-二甲氨基吡啶 作用下， 以 乙醚 、 二氯甲烷 为溶剂， 以39%的产率得到2-propanone-1,3-di-t-butyldicarbonate
  参考文献：
  名称：

  6-11 bicyclic ketolide derivatives

  摘要：

  本发明揭示了公式I的化合物，或其药学上可接受的盐，酯或前药：这些化合物具有抗菌特性。本发明还涉及包含上述化合物的制药组合物，用于治疗需要抗生素治疗的受体。本发明还涉及通过给予含有本发明化合物的制药组合物来治疗受体的细菌感染的方法。本发明还包括制备本发明化合物的方法。

  公开号：

  US06878691B2

文献信息

• [EN] 6-11 BICYCLIC KETOLIDE DERIVATIVES<br/>[FR] DERIVES DE CETOLIDE 6-11 BICYCLIQUES
  申请人：ENANTA PHARM INC

  公开号：WO2003097659A1

  公开（公告）日：2003-11-27

  The present invention discloses compounds of formula (I), or pharmaceutically acceptable salts, esters, or prodrugs thereof: which exhibit antibacterial properties. The present invention further relates to pharmaceutical compositions comprising the aforementioned compounds for administration to a subject in need of antibiotic treatment. The invention also relates to methods of treating a bacterial infection in a subject by administering a pharmaceutical composition comprising the compounds of the present invention. The invention further includes process by which to make the compounds of the present invention.

  本发明公开了以下式(I)的化合物，或其药学上可接受的盐、酯或前药：具有抗菌性能。本发明还涉及包含上述化合物的药物组合物，用于给需要抗生素治疗的受试者使用。该发明还涉及通过给受试者使用包含本发明化合物的药物组合物来治疗受试者的细菌感染的方法。该发明还包括制备本发明化合物的方法。
• [EN] 6,11 BICYCLIC ERYTHROMYCIN DERIVATIVES<br/>[FR] DERIVES DE L'ERYTHROMYCINE 6,11 BICYCLIQUE
  申请人：ENANTA PHARM INC

  公开号：WO2003095466A1

  公开（公告）日：2003-11-20

  The present invention discloses compounds of formula (I), or pharmaceutically acceptable salts, esters, or prodrugs thereof which exhibit antibacterial properties. The present invention further relates to pharmaceutical compositions comprising the aforementioned compounds for administration to a subject in need of antibiotic treatment. The invention also relates to methods of treating a bacterial infection in a subject by administering a pharmaceutical composition comprising the compounds of the present invention. The invention further includes process by which to make the compounds of the present invention.

  本发明公开了具有抗菌性质的化合物(I)的公式，或其药学上可接受的盐、酯或前药。本发明还涉及包含上述化合物的药物组合物，用于治疗需要抗生素治疗的受试者。该发明还涉及通过给予包含本发明化合物的药物组合物来治疗受试者的细菌感染的方法。该发明还包括制备本发明化合物的方法。
• [EN] 6-11 BICYCLIC KETOLIDE DERIVATIVES<br/>[FR] DERIVES KETOLIDES BICYCLIQUES 6-11
  申请人：ENANTA PHARM INC

  公开号：WO2005061525A1

  公开（公告）日：2005-07-07

  The present invention discloses compounds of formula I, or pharmaceutically acceptable salts, esters, or prodrugs thereof: (I) which exhibit antibacterial properties. The present invention further relates to pharmaceutical compositions comprising the aforementioned compounds for administration to a subject in need of antibiotic treatment. The invention also relates to methods of treating a bacterial infection in a subject by administering a pharmaceutical composition comprising the compounds of the present invention. The invention further includes process by which to make the compounds of the present invention.

  本发明公开了具有以下结构的化合物，或其药学上可接受的盐、酯或前药：(I)，这些化合物具有抗菌性能。本发明还涉及包含上述化合物的药物组合物，用于给需要抗生素治疗的受试者进行治疗。该发明还涉及通过给予包含本发明化合物的药物组合物来治疗受试者的细菌感染的方法。该发明还包括制备本发明化合物的方法。
• 6-11 Bicyclic ketolide derivatives
  申请人：Or Sun Yat

  公开号：US20050037982A1

  公开（公告）日：2005-02-17

  The present invention discloses compounds of formula I, or pharmaceutically acceptable salts, esters, or prodrugs thereof: which exhibit antibacterial properties. The present invention further relates to pharmaceutical compositions comprising the aforementioned compounds for administration to a subject in need of antibiotic treatment. The invention also relates to methods of treating a bacterial infection in a subject by administering a pharmaceutical composition comprising the compounds of the present invention. The invention further includes process by which to make the compounds of the present invention.

  本发明揭示了公式I的化合物，或其药学上可接受的盐、酯或前药：其具有抗菌性能。本发明还涉及包含上述化合物的制药组合物，用于给需要抗生素治疗的受体进行治疗。本发明还涉及通过给予包含本发明化合物的制药组合物来治疗受体中的细菌感染的方法。本发明还包括制备本发明化合物的方法。
• Synthesis of Novel 6,11-O-Bridged Bicyclic Ketolides via a Palladium-Catalyzed Bis-allylation
  作者：Guoqiang Wang、Deqiang Niu、Yao-Ling Qiu、Ly Tam Phan、Zhigang Chen、Alexander Polemeropoulos、Yat Sun Or

  DOI：10.1021/ol048336r

  日期：2004.11.1

  A bridging chemistry process was developed to form an ether bridge between 6-O and 11-O of erythromycin A via a tandem or stepwise palladium-catalyzed bis-pi-allylation. By applying this bridging process, new 6,11-O-bridged bicyclic ketolides (BBKs) were synthesized. These BBKs showed good antibacterial activities against the macrolide-susceptible strains as well as mef-resistant strains and served as a good core for further modifications to study the structure-activity relationship (SAR) and to overcome bacterial resistance.