(2R,3S)-methyl 2-(2-(isopropylsulfonyl)-5-(methoxycarbonyl)phenyl)pyrrolidine-3-carboxylate hydrochloride salt | 900174-79-0

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 哌啶类
• 英文名称: (2R,3S)-methyl 2-(2-(isopropylsulfonyl)-5-(methoxycarbonyl)phenyl)pyrrolidine-3-carboxylate hydrochloride salt
• 英文别名: (2R,3S)-methyl 2-(2-(isopropylsulfonyl)-5-(methoxycarbonyl)phenyl)pyrrolidine-3-carboxylate hydrochloride salt；(2R,3S)-methyl 2-(2-(isopropylsulfonyl)-5-(methoxycarbonyl)phenyl)pyrrolidine-3-carboxylate hydrochloride
• CAS: 900174-79-0
• 化学式: C₁₇H₂₄N₂O₆S*ClH
• 分子量: 420.914
• InChiKey: NYUBREPQHKUTOM-SBKWZQTDSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.29
• 重原子数：
  27.0
• 可旋转键数：
  5.0
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.53
• 拓扑面积：
  110.8
• 氢给体数：
  2.0
• 氢受体数：
  7.0

反应信息

• 作为反应物：
  描述：

  (2R,3S)-methyl 2-(2-(isopropylsulfonyl)-5-(methoxycarbonyl)phenyl)pyrrolidine-3-carboxylate hydrochloride salt 在 盐酸 、 盐酸-N-乙基-Nˊ-(3-二甲氨基丙基)碳二亚胺 、 N,N-二异丙基乙胺 、 sodium hydroxide 作用下， 以 四氢呋喃 、 1,4-二氧六环 、 甲醇 、 水 、 乙酸乙酯 为溶剂， 反应 5.0h， 生成 (2R,3S)-1-((R)-2-(1-aminoisoquinolin-6-ylamino)-2-(5-ethoxy-2-fluorophenyl)acetyl)-2-(2-(isopropylsulfonyl)-5-(methoxycarbonyl)phenyl)-pyrrolidine-3-carboxylic acid trifluoroacetic acid salt
  参考文献：
  名称：

  Design and Synthesis of Phenylpyrrolidine Phenylglycinamides As Highly Potent and Selective TF-FVIIa Inhibitors

  摘要：

  Inhibitors of the Tissue Factor/Factor VIIa (TF-FVIIa) complex are promising novel anticoagulants that show excellent efficacy and minimal bleeding in preclinical models. On the basis of a zwitterionic phenylglycine acylsulfonamide 1, a phenylglycine benzylamide 2 was shown to possess improved permeability and oral bioavailability. Optimization of the benzylamide, guided by X-ray crystallography, led to a potent TF-FVIIa inhibitor 18i with promising oral bioavailability, but promiscuous activity in an in vitro safety panel of receptors and enzymes. Introducing an acid on the pyrrolidine ring, guided by molecular modeling, resulted in highly potent, selective, and efficacious TF-FVIIa inhibitors with clean in vitro safety profile. The pyrrolidine acid 20 showed a moderate clearance, low volume of distribution, and a short t(1/2) in dog PK studies.

  DOI：

  10.1021/ml400453z
• 作为产物：
  描述：

  1-tert-butyl-3-methyl 2-(2-(isopropylthio)-5-nitrophenyl)pyrrolidine-1,3-dicarboxylate 在 吡啶 、 palladium 10% on activated carbon 、 氢气 、 碳酸氢钠 、 间氯过氧苯甲酸 作用下， 以 四氢呋喃 、 甲醇 、 二氯甲烷 为溶剂， 反应 9.5h， 生成 (2R,3S)-methyl 2-(2-(isopropylsulfonyl)-5-(methoxycarbonyl)phenyl)pyrrolidine-3-carboxylate hydrochloride salt
  参考文献：
  名称：

  Design and Synthesis of Phenylpyrrolidine Phenylglycinamides As Highly Potent and Selective TF-FVIIa Inhibitors

  摘要：

  Inhibitors of the Tissue Factor/Factor VIIa (TF-FVIIa) complex are promising novel anticoagulants that show excellent efficacy and minimal bleeding in preclinical models. On the basis of a zwitterionic phenylglycine acylsulfonamide 1, a phenylglycine benzylamide 2 was shown to possess improved permeability and oral bioavailability. Optimization of the benzylamide, guided by X-ray crystallography, led to a potent TF-FVIIa inhibitor 18i with promising oral bioavailability, but promiscuous activity in an in vitro safety panel of receptors and enzymes. Introducing an acid on the pyrrolidine ring, guided by molecular modeling, resulted in highly potent, selective, and efficacious TF-FVIIa inhibitors with clean in vitro safety profile. The pyrrolidine acid 20 showed a moderate clearance, low volume of distribution, and a short t(1/2) in dog PK studies.

  DOI：

  10.1021/ml400453z

文献信息

• BENZAMIDE FACTOR VIIA INHIBITORS USEFUL AS ANTICOAGULANTS
  申请人：Priestley Eldon Scott

  公开号：US20100227894A1

  公开（公告）日：2010-09-09

  The present invention provides novel benzamide derivatives of Formula (I): or a stereoisomer, tautomer, pharmaceutically acceptable salt, solvate, or prodrug thereof, wherein the variables A, W, Y, Z, R 8 , and R 9 are as defined herein. These compounds are selective inhibitors of factor VIIa which can be used as medicaments.

  本发明提供了式(I)的新型苯甲酰胺衍生物：或其立体异构体、互变异构体、药学上可接受的盐、溶剂合物或前药，其中变量A、W、Y、Z、R8和R9如本文所定义。这些化合物是选择性因子VIIa的抑制剂，可用作药物。
• WO2006/76246
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• WO2008/79759
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