Methyl 2-fluoro-4-piperidin-2-ylbenzoate | 1337517-09-5

• 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: Methyl 2-fluoro-4-piperidin-2-ylbenzoate
• CAS: 1337517-09-5
• 化学式: C₁₃H₁₆FNO₂
• 分子量: 237.274
• InChiKey: KHGWMCHBTVWSTF-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.1
• 重原子数：
  17
• 可旋转键数：
  3
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.46
• 拓扑面积：
  38.3
• 氢给体数：
  1
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  Methyl 2-fluoro-4-piperidin-2-ylbenzoate 、 氯甲酸苄酯 在 potassium carbonate 作用下， 以 1,4-二氧六环 、 水 为溶剂， 反应 4.0h， 以7.5 g的产率得到benzyl 2-(3-fluoro-4-(methoxycarbonyl)-phenyl)piperidine-1-carboxylate
  参考文献：
  名称：

  Optimization of Phenyl-Substituted Benzimidazole Carboxamide Poly(ADP-Ribose) Polymerase Inhibitors: Identification of (S)-2-(2-Fluoro-4-(pyrrolidin-2-yl)phenyl)-1H-benzimidazole-4-carboxamide (A-966492), a Highly Potent and Efficacious Inhibitor

  摘要：

  We have developed a series of phenylpyrrolidine- and phenylpiperidine-substituted benzimidazole carboxamide poly(ADP-ribose) polymerase (PARP) inhibitors with excellent PARP enzyme potency as well as single-digit nanomolar cellular potency. These efforts led to the identification of (S)-2-(2-fluoro-4-(pyrrolidin-2-yl)phenyl)-1H-benzimidazole-4-carboxamide (22b, A-966492). Compound 22b displayed excellent potency against the PARP-1 enzyme with a K-i of 1 nM and an EC50 of 1 nM in a whole cell assay. In addition, 22b is orally bioavailable across multiple species, crosses the blood brain barrier, and appears to distribute into tumor tissue. It also demonstrated good in vivo efficacy in a B16F10 subcutaneous murine melanoma model in combination with temozolomide and in an MX-1 breast cancer xenograft model both as a single agent and in combination with carboplatin.

  DOI：

  10.1021/jm901775y
• 作为产物：
  描述：

  methyl 2-fluoro-4-(pyridin-2-yl)benzoate 在 platinum on carbon 、 氢气 作用下， 以 甲醇 为溶剂， 反应 10.0h， 生成 Methyl 2-fluoro-4-piperidin-2-ylbenzoate
  参考文献：
  名称：

  Optimization of Phenyl-Substituted Benzimidazole Carboxamide Poly(ADP-Ribose) Polymerase Inhibitors: Identification of (S)-2-(2-Fluoro-4-(pyrrolidin-2-yl)phenyl)-1H-benzimidazole-4-carboxamide (A-966492), a Highly Potent and Efficacious Inhibitor

  摘要：

  We have developed a series of phenylpyrrolidine- and phenylpiperidine-substituted benzimidazole carboxamide poly(ADP-ribose) polymerase (PARP) inhibitors with excellent PARP enzyme potency as well as single-digit nanomolar cellular potency. These efforts led to the identification of (S)-2-(2-fluoro-4-(pyrrolidin-2-yl)phenyl)-1H-benzimidazole-4-carboxamide (22b, A-966492). Compound 22b displayed excellent potency against the PARP-1 enzyme with a K-i of 1 nM and an EC50 of 1 nM in a whole cell assay. In addition, 22b is orally bioavailable across multiple species, crosses the blood brain barrier, and appears to distribute into tumor tissue. It also demonstrated good in vivo efficacy in a B16F10 subcutaneous murine melanoma model in combination with temozolomide and in an MX-1 breast cancer xenograft model both as a single agent and in combination with carboplatin.

  DOI：

  10.1021/jm901775y

文献信息

• Piperidinyl-Indole Derivatives Complement Factor B Inhibitors and Uses Thereof
  申请人：ADAMS Christopher

  公开号：US20160152605A1

  公开（公告）日：2016-06-02

  The present invention provides a compound of formula I: (I) a method for manufacturing the compounds of the invention, and its therapeutic uses as inhibitors of the complement alternative pathway, in particular of Factor B. The present invention further provides a combination of pharmacologically active agents and a pharmaceutical composition.

  本发明提供了一种公式I的化合物：(I)，一种用于制造本发明化合物的方法，并且本发明化合物具有治疗作用，可作为替代途径补体的抑制剂，特别是因子B的抑制剂。本发明还提供了一种药理活性剂的组合和一种制药组合物。
• PIPERIDINYL-INDOLE DERIVATIVES COMPLEMENT FACTOR B INHIBITORS AND USES THEREOF
  申请人：Novartis AG

  公开号：EP3299365A1

  公开（公告）日：2018-03-28

  The present invention provides a compound of formula I: a method for manufacturing the compounds of the invention, and its therapeutic uses. The present invention further provides a combination of pharmacologically active agents and a pharmaceutical composition.

  本发明提供了一种式 I 的化合物： 一种制造本发明化合物的方法及其治疗用途。本发明进一步提供了一种药理活性剂组合和药物组合物。
• Piperidinyl-indole derivatives complement factor B inhibitors and uses thereof
  申请人：Novartis AG

  公开号：US10093663B2

  公开（公告）日：2018-10-09

  The present invention provides a compound of formula I: a method for manufacturing the compounds of the invention, and its therapeutic uses. The present invention further provides a combination of pharmacologically active agents and a pharmaceutical composition.

  本发明提供了一种式 I 的化合物： 一种制造本发明化合物的方法及其治疗用途。本发明还提供了一种药理活性剂组合和药物组合物。
• PIPERIDINYL INDOLE DERIVATIVES AND THEIR USE AS COMPLEMENT FACTOR B INHIBITORS
  申请人：Novartis AG

  公开号：EP3022192B1

  公开（公告）日：2017-10-11
• US9682968B2
  申请人：——

  公开号：US9682968B2

  公开（公告）日：2017-06-20