2-Ethyl-2-[(3S,4R)-3-(3-fluoro-phenyl)-4-formyl-pyrrolidin-1-ylmethyl]-butyric acid benzyl ester | 442876-64-4

• 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-Ethyl-2-[(3S,4R)-3-(3-fluoro-phenyl)-4-formyl-pyrrolidin-1-ylmethyl]-butyric acid benzyl ester
• 英文别名: 2-{[(3R,4S)-3-Formyl-4-(3-fluorophenyl)pyrrolidin-1-yl]methyl}-2-ethylbutyric Acid, Benzyl Ester；benzyl 2-ethyl-2-[[(3S,4R)-3-(3-fluorophenyl)-4-formylpyrrolidin-1-yl]methyl]butanoate
• CAS: 442876-64-4
• 化学式: C₂₅H₃₀FNO₃
• 分子量: 411.517
• InChiKey: NWLMVCJSKLQHOB-FYYLOGMGSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4.3
• 重原子数：
  30
• 可旋转键数：
  10
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.44
• 拓扑面积：
  46.6
• 氢给体数：
  0
• 氢受体数：
  5

反应信息

• 作为反应物：
  描述：

  2-Ethyl-2-[(3S,4R)-3-(3-fluoro-phenyl)-4-formyl-pyrrolidin-1-ylmethyl]-butyric acid benzyl ester 在 palladium on activated charcoal 氢气 、 三乙酰氧基硼氢化钠 作用下， 以 甲醇 、 二氯甲烷 为溶剂， 反应 3.0h， 生成 2-{[(3S,4S)-3-[(4-{3-Benzyl-1-ethyl-1H-pyrazol-5-yl}piperidin-1-yl)methyl]-4-(3-fluorophenyl)pyrrolidin-1-yl]methyl}-2-ethylbutyric Acid
  参考文献：
  名称：

  CCR5 Antagonists:  3-(Pyrrolidin-1-yl)propionic Acid Analogues with Potent Anti-HIV Activity

  摘要：

  graphicA novel approach to alpha,alpha-disubstituted-beta-amino acids (beta(2,2)-amino acids) was employed in the synthesis of a series of 3-(pyrrolidin-1-yl)-propionic acids possessing high affinity for the CCR5 receptor and potent anti-HIV activity. The rat pharmacokinetics for these new analogues featured higher bioavailabilities and lower rates of clearance as compared to cyclopentane 1.

  DOI：

  10.1021/ol034707c
• 作为产物：
  描述：

  2-Ethyl-2-[(3S,4R)-3-(3-fluoro-phenyl)-4-hydroxymethyl-pyrrolidin-1-ylmethyl]-butyric acid benzyl ester 在 草酰氯 、 二甲基亚砜 、 N,N-二异丙基乙胺 作用下， 以 二氯甲烷 为溶剂， 生成 2-Ethyl-2-[(3S,4R)-3-(3-fluoro-phenyl)-4-formyl-pyrrolidin-1-ylmethyl]-butyric acid benzyl ester
  参考文献：
  名称：

  CCR5 Antagonists:  3-(Pyrrolidin-1-yl)propionic Acid Analogues with Potent Anti-HIV Activity

  摘要：

  graphicA novel approach to alpha,alpha-disubstituted-beta-amino acids (beta(2,2)-amino acids) was employed in the synthesis of a series of 3-(pyrrolidin-1-yl)-propionic acids possessing high affinity for the CCR5 receptor and potent anti-HIV activity. The rat pharmacokinetics for these new analogues featured higher bioavailabilities and lower rates of clearance as compared to cyclopentane 1.

  DOI：

  10.1021/ol034707c

文献信息

• Pyrrolidine modulators of CCR5 chemokine receptor activity
  申请人：——

  公开号：US20020094989A1

  公开（公告）日：2002-07-18

  Pyrrolidine compounds of Formula I: 1 (wherein 1 , R 2 , R 3 , R 4 , R 5 ,R 6a , R 6b , R 7 and R 8 are defined herein) are described. The compounds are modulators of CCR5 chemokine receptor activity. The compounds are useful, for example, in the prevention or treatment of infection by HIV and the treatment of AIDS, as compounds or pharmaceutically acceptable salts, or as ingredients in pharmaceutical compositions, optionally in combination with other antivirals, immunomodulators, antibiotics or vaccines. Methods of treating AIDS and methods of preventing or treating infection by HIV are also described.

  描述了式子I：1中的吡咯烷化合物（其中1、R2、R3、R4、R5、R6a、R6b、R7和R8在此定义）。这些化合物是CCR5趋化因子受体活性的调节剂。这些化合物可用于预防或治疗HIV感染和治疗艾滋病，作为化合物或药物可接受的盐，或作为制药组合物的成分，可选择与其他抗病毒药物、免疫调节剂、抗生素或疫苗组合使用。还描述了治疗艾滋病的方法和预防或治疗HIV感染的方法。