methyl 2-chloro-5-[3-[[2-(cyclopropylmethyl)-1-oxo-3H-isoindol-5-yl]oxymethyl]phenyl]benzoate | 1260224-99-4

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 英文名称: methyl 2-chloro-5-[3-[[2-(cyclopropylmethyl)-1-oxo-3H-isoindol-5-yl]oxymethyl]phenyl]benzoate
• CAS: 1260224-99-4
• 化学式: C₂₇H₂₄ClNO₄
• 分子量: 461.945
• InChiKey: OVEGJHUCKYNPRO-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  5.3
• 重原子数：
  33
• 可旋转键数：
  8
• 环数：
  5.0
• sp3杂化的碳原子比例：
  0.26
• 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：

  methyl 2-chloro-5-[3-[[2-(cyclopropylmethyl)-1-oxo-3H-isoindol-5-yl]oxymethyl]phenyl]benzoate 在 水 、 lithium hydroxide 作用下， 以 四氢呋喃 为溶剂， 以39%的产率得到4-chloro-3'-((2-(cyclopropylmethyl)-1-oxoisoindolin-5-yloxy)methyl)biphenyl-3-carboxylic acid
  参考文献：
  名称：

  Design and Synthesis of an Orally Active Metabotropic Glutamate Receptor Subtype-2 (mGluR2) Positive Allosteric Modulator (PAM) That Decreases Cocaine Self-Administration in Rats

  摘要：

  The modification of 3'((2-cyclopentyl-6,7-dimethyl-1-oxo-2,3-dihydro-1 H-inden-5-yloxy)methyl)biphenyl 4-carboxylic acid (BINA, 1) by incorporating heteroatoms into the structure and replacing the cyclopentyl moiety led to the development of new mGluR2 positive allosteric modulators (PAMs) with optimized potency and superior druglike properties These analogues are more potent than 1 in vitro and are highly selective for mGluR2 vs other mGluR subtypes They have significantly improved pharmacokinetic (PK) properties, with excellent oral bioavailability and brain penetration The benzisothiazol-3-one derivative 14 decreased cocaine self-administration in rats, providing proof-of-concept for the use of mGluR2 PAMs for the treatment of cocaine dependence

  DOI：

  10.1021/jm1012165
• 作为产物：
  描述：

  4-羟基邻苯二甲酸 在 potassium carbonate 、 溶剂黄146 、 锌 作用下， 以 丙酮 、 甲苯 为溶剂， 反应 12.08h， 生成 methyl 2-chloro-5-[3-[[2-(cyclopropylmethyl)-1-oxo-3H-isoindol-5-yl]oxymethyl]phenyl]benzoate
  参考文献：
  名称：

  Design and Synthesis of an Orally Active Metabotropic Glutamate Receptor Subtype-2 (mGluR2) Positive Allosteric Modulator (PAM) That Decreases Cocaine Self-Administration in Rats

  摘要：

  The modification of 3'((2-cyclopentyl-6,7-dimethyl-1-oxo-2,3-dihydro-1 H-inden-5-yloxy)methyl)biphenyl 4-carboxylic acid (BINA, 1) by incorporating heteroatoms into the structure and replacing the cyclopentyl moiety led to the development of new mGluR2 positive allosteric modulators (PAMs) with optimized potency and superior druglike properties These analogues are more potent than 1 in vitro and are highly selective for mGluR2 vs other mGluR subtypes They have significantly improved pharmacokinetic (PK) properties, with excellent oral bioavailability and brain penetration The benzisothiazol-3-one derivative 14 decreased cocaine self-administration in rats, providing proof-of-concept for the use of mGluR2 PAMs for the treatment of cocaine dependence

  DOI：

  10.1021/jm1012165

文献信息

• Design and Synthesis of an Orally Active Metabotropic Glutamate Receptor Subtype-2 (mGluR2) Positive Allosteric Modulator (PAM) That Decreases Cocaine Self-Administration in Rats
  作者：Raveendra-Panickar Dhanya、Shyama Sidique、Douglas J. Sheffler、Hilary Highfield Nickols、Ananda Herath、Li Yang、Russell Dahl、Robert Ardecky、Svetlana Semenova、Athina Markou、P. Jeffrey Conn、Nicholas D. P. Cosford

  DOI：10.1021/jm1012165

  日期：2011.1.13

  The modification of 3'((2-cyclopentyl-6,7-dimethyl-1-oxo-2,3-dihydro-1 H-inden-5-yloxy)methyl)biphenyl 4-carboxylic acid (BINA, 1) by incorporating heteroatoms into the structure and replacing the cyclopentyl moiety led to the development of new mGluR2 positive allosteric modulators (PAMs) with optimized potency and superior druglike properties These analogues are more potent than 1 in vitro and are highly selective for mGluR2 vs other mGluR subtypes They have significantly improved pharmacokinetic (PK) properties, with excellent oral bioavailability and brain penetration The benzisothiazol-3-one derivative 14 decreased cocaine self-administration in rats, providing proof-of-concept for the use of mGluR2 PAMs for the treatment of cocaine dependence