2(S)-[acetoxymethyl]-1-[chloromethyloxycarbonyl]pyrrolidine | 338990-23-1

• 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(S)-[acetoxymethyl]-1-[chloromethyloxycarbonyl]pyrrolidine
• 英文别名: chloromethyl (2S)-2-(acetyloxymethyl)pyrrolidine-1-carboxylate
• CAS: 338990-23-1
• 化学式: C₉H₁₄ClNO₄
• 分子量: 235.667
• InChiKey: AVLIGFWZQUEATB-QMMMGPOBSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.3
• 重原子数：
  15
• 可旋转键数：
  5
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.78
• 拓扑面积：
  55.8
• 氢给体数：
  0
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  2(S)-[acetoxymethyl]-1-[chloromethyloxycarbonyl]pyrrolidine 、 艾沙康唑 在 sodium iodide 作用下， 以 乙腈 为溶剂， 以92%的产率得到[[2(S)-(acetoxymethyl)pyrrolidin-1-yl]carbonyloxy]methyl-1-[(2R,3R)-2-(2,5-difluorophenyl)-2-hydroxy-3-[4-(4-cyanophenyl)thiazol-2-yl]butyl]-1H-[1,2,4]triazol-4-ium iodide
  参考文献：
  名称：

  Design, synthesis and antifungal activity of a novel water soluble prodrug of antifungal triazole

  摘要：

  A highly potent water soluble triazole antifungal prodrug, RO0098557 (1), has been identified from its parent, the novel antifungal agent RO0094815 (2). The prodrug includes a triazolium salt linked to an aminocarboxyl moiety, which undergoes enzymatic activation followed by spontaneous chemical degradation to release 2. Prodrug 1 showed high chemical stability and water solubility and exhibited strong antifungal activity against systemic candidiasis and aspergillosis as well as pulmonary aspergillosis in rats. (C) 2002 Elsevier Science Ltd. All rights reserved.

  DOI：

  10.1016/s0960-894x(02)00892-2
• 作为产物：
  描述：

  L-脯氨醇 在 吡啶 、 三乙胺 作用下， 以 二氯甲烷 为溶剂， 生成 2(S)-[acetoxymethyl]-1-[chloromethyloxycarbonyl]pyrrolidine
  参考文献：
  名称：

  Design, synthesis and antifungal activity of a novel water soluble prodrug of antifungal triazole

  摘要：

  A highly potent water soluble triazole antifungal prodrug, RO0098557 (1), has been identified from its parent, the novel antifungal agent RO0094815 (2). The prodrug includes a triazolium salt linked to an aminocarboxyl moiety, which undergoes enzymatic activation followed by spontaneous chemical degradation to release 2. Prodrug 1 showed high chemical stability and water solubility and exhibited strong antifungal activity against systemic candidiasis and aspergillosis as well as pulmonary aspergillosis in rats. (C) 2002 Elsevier Science Ltd. All rights reserved.

  DOI：

  10.1016/s0960-894x(02)00892-2

文献信息

• [EN] COMPOUNDS AND THERAPEUTIC USES THEREOF<br/>[FR] COMPOSÉS ET LEURS UTILISATIONS THÉRAPEUTIQUES
  申请人：ALZHEIMER S INST OF AMERICA INC

  公开号：WO2014004884A1

  公开（公告）日：2014-01-03

  The invention relates to compounds, pharmaceutical compositions and methods useful for treating cancer, systemic or chronic inflammation, rheumatoid arthritis, diabetes, obesity, T-cell mediated autoimmune disease, ischemia, and other complications associated with these diseases and disorders.

  这项发明涉及化合物、药物组合物和方法，用于治疗癌症、全身性或慢性炎症、类风湿性关节炎、糖尿病、肥胖症、T细胞介导的自身免疫疾病、缺血以及与这些疾病和疾病相关并发症。
• Intermediates for N-substituted carbamoyloxyalkyl-azolium derivatives
  申请人：Fukuda Hiroshi

  公开号：US20050038075A1

  公开（公告）日：2005-02-17

  N-substituted carbamoyloxyalkyl-azolium derivatives which have antifungal activity and are useful for the treatment of fungal diseases.

  N-取代的碳酰氧基烷基-唑类衍生物具有抗真菌活性，可用于治疗真菌病。
• N-phenyl substituted carbamoyloxyalkyl-azolium derivatives
  申请人：Fukuda Hiroshi

  公开号：US20050038038A1

  公开（公告）日：2005-02-17

  N-substituted carbamoyloxyalkyl-azolium derivatives Which have antifungal activity and are useful for the treatment of fungal diseases.

  N-取代的氨基甲酰氧基烷基-唑烷盐衍生物，具有抗真菌活性，可用于治疗真菌病。
• N-substituted carbamoyloxyalkyl-azolium derivatives
  申请人：Fukuda Hiroshi

  公开号：US20070027322A1

  公开（公告）日：2007-02-01

  N-substituted carbamoyloxyalkyl-azolium derivatives which have antifungal activity and are useful for the treatment of fungal diseases.

  N-取代的氨基甲酰氧烷基-唑状衍生物具有抗真菌活性，可用于治疗真菌病。
• N-SUBSTITUTED CARBAMOYLOXYALKYL-AZOLIUM DERIVATIVES
  申请人：Basilea Pharmaceutica AG

  公开号：EP1280795A2

  公开（公告）日：2003-02-05