2,2,2-trifluoro-N-(4-fluoro-3-pyridin-4-yl-benzyl)-acetamide hydrochloride | 1208977-19-8

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 吡啶及其衍生物
• 英文名称: 2,2,2-trifluoro-N-(4-fluoro-3-pyridin-4-yl-benzyl)-acetamide hydrochloride
• 英文别名: 2,2,2-trifluoro-N-(4-fluoro-3-pyridin-4-yl-benzyl)acetamide hydrochloride；2,2,2-trifluoro-N-(4-fluoro-3-pyridin-4-ylbenzyl)acetamide hydrochloride；2,2,2-trifluoro-N-[(4-fluoro-3-pyridin-4-ylphenyl)methyl]acetamide;hydrochloride
• CAS: 1208977-19-8
• 化学式: C₁₄H₁₀F₄N₂O*ClH
• 分子量: 334.701
• InChiKey: ZTYPULSVPPCCAY-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.49
• 重原子数：
  22
• 可旋转键数：
  3
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.14
• 拓扑面积：
  42
• 氢给体数：
  2
• 氢受体数：
  6

反应信息

• 作为反应物：
  描述：

  2,2,2-trifluoro-N-(4-fluoro-3-pyridin-4-yl-benzyl)-acetamide hydrochloride 在 铂 氢气 、 乙酸丁酯 、 甲醇 作用下， 以 甲醇 为溶剂， 10.0~50.0 ℃ 、18.38 MPa 条件下， 反应 83.0h， 以to give 112 g (89%) of compound 14 as white solid的产率得到2,2,2-trifluoro-N-(4-fluoro-3-piperidin-4-yl-benzyl)acetamide hydrochloride
  参考文献：
  名称：

  Method and intermediates for the preparation of 2,2,2-trifluoro-N-(4-fluoro-3-pyridin-4-yl-benzyl)-acetamide hydrochloride

  摘要：

  本发明涉及一种制备2,2,2-三氟-N-(4-氟-3-吡啶-4-基苄基)乙酰胺盐酸盐的方法，以及在该方法中使用的反应中间体。

  公开号：

  US08497379B2
• 作为产物：
  描述：

  4-fluoro-3-pyridin-4-yl-benzylamine 、 三氟乙酸酐 在 sodium carbonate 、 盐酸 作用下， 以 乙酸丁酯 、 水 为溶剂， 生成 2,2,2-trifluoro-N-(4-fluoro-3-pyridin-4-yl-benzyl)-acetamide hydrochloride
  参考文献：
  名称：

  [EN] [4-(5-AMINOMETHYL-2-FLUORO-PHENYL)-PIPERIDIN-1-YL]-[7-FLUORO-1-(2-METHOXY-ETHYL)-4-TRIFLUOROMETHOXY-1H-INDOL-3-YL]-METHANONE AS AN INHIBITOR OF MAST CELL TRYPTASE
  [FR] [4-(5-AMINOMÉTHYL-2-FLUORO-PHÉNYL)-PIPÉRIDIN-1-YL]-[7-FLUORO-1-(2-MÉTHOXY-ÉTHYL)-4-TRIFLUOROMÉTHOXY-1H-INDOL-3-YL]-MÉTHANONE EN TANT QU'INHIBITEUR DE LA TRYPTASE DE MASTOCYTES

  摘要：

  公开号：

  WO2010022196A3

文献信息

• [EN] INDOLYL-PIPERIDINYL BENZYLAMINES AS BETA-TRYPTASE INHIBITORS<br/>[FR] INDOLYL-PIPÉRIDINYL BENZYLAMINES INHIBITRICES DE LA BÊTA-TRYPTASE
  申请人：SANOFI SA

  公开号：WO2011079102A1

  公开（公告）日：2011-06-30

  The present invention discloses and claims a series of substituted indolyl-piperidinyl benzylamines of formula (I), wherein R1, R2 and R3 are as described herein. More specifically, the compounds of this invention are inhibitors of β-tryptase and are, therefore, useful as pharmaceutical agents. Additionally, this invention also discloses methods of preparation of substituted indolyl-piperidinyl benzylamines. In one of the embodiments, there is provided the compounds of formula (I) wherein R3 is (II).

  本发明公开并要求一系列取代的吲哚基-哌啶基苄胺化合物，其公式为（I），其中R1、R2和R3如本文所述。更具体地说，本发明的化合物是β-tryptase的抑制剂，因此可用作药物制剂。此外，本发明还公开了取代的吲哚基-哌啶基苄胺的制备方法。在其中一个实施例中，提供了公式（I）的化合物，其中R3是（II）。
• [EN] [4[4-(5-AMINOMETHYL-2-FLUORO-PHENYL)-PIPERIDIN-1-YL]-(1H-PYRROLO-PYRIDIN-YL)-METHANONES AND SYNTHESIS THEREOF<br/>[FR] [4[4-(5-AMINOMÉTHYL-2-FLUORO-PHÉNYL)-PIPÉRIDIN-1-YL]-(1H-PYRROLO-PYRIDIN-YL)-MÉTHANONES ET LEUR SYNTHÈSE
  申请人：SANOFI SA

  公开号：WO2011078984A1

  公开（公告）日：2011-06-30

  The present invention relates herein to compounds and compositions for the treatment and amelioration of inflammatory disease. Specifically the present invention relates to compounds that having a tryptase inhibition activity and the intermediates thereof, pharmaceutical compositions comprising such compounds, and a method of treating subjects suffering from a condition disease or disorder that can be ameliorated by the administration of an inhibitor of tryptase including but not limited to for example asthma and other inflammatory diseases including age-related macular degeneration.

  本发明涉及用于治疗和改善炎症性疾病的化合物和组合物。特别是，本发明涉及具有胰蛋白酶抑制活性的化合物及其中间体，包括这些化合物的药物组合物，以及治疗可通过施用胰蛋白酶抑制剂来改善的状况、疾病或失调的方法，例如但不限于哮喘和其他炎症性疾病，包括年龄相关的黄斑变性。
• [EN] DISUBSTITUTED [4-(5-AMINOMETHYL-PHENYL)-PIPERIDIN-1-YL]-1H-INDOL-3-YL]-METHANONES<br/>[FR] [4-(5-AMINOMÉTHYL-PHÉNYL)-PIPÉRIDIN-1-YL]-1H-INDOL-3-YL]-MÉTHANONES DISUBSTITUÉES
  申请人：SANOFI AVENTIS

  公开号：WO2011022449A1

  公开（公告）日：2011-02-24

  The present invention extends to the compound of formula I: or a prodrug, pharmaceutically acceptable salt, or solvate of said compound. Furthermore, the present invention is directed to a pharmaceutical composition comprising a pharmaceutically effective amount of the compound of formula I, and a pharmaceutically acceptable carrier. Furthermore, the present invention is directed to the use of a compound of formula I as an inhibitor of tryptase, comprising introducing the compound into a composition comprising tryptase. In addition, the present invention is directed to the use of a compound of formula I for treating a patient suffering from, or subject to, a physiological condition in need of amelioration of an inhibitor of tryptase comprising administering to the patient a therapeutically effective amount of the compound of Claim 1. The present invention is directed also to the preparation of a compound of formula I.

  本发明涉及到式I的化合物：或者该化合物的前药、药用可接受的盐或溶剂。此外，本发明涉及一种包括式I化合物的药物组合物，以及药用可接受的载体的药学有效量。此外，本发明涉及将式I化合物用作色氨酸蛋白酶抑制剂的用途，包括将该化合物引入含有色氨酸蛋白酶的组合物中。此外，本发明还涉及将式I化合物用于治疗患有或患有需要改善色氨酸蛋白酶抑制剂的生理状况的患者的用途，包括向患者施用权利要求1中的化合物的治疗有效量。本发明还涉及制备式I化合物。
• [4 [4-(AMINOMETHYL-2-FLUORO-PHENYL)-PIPERIDIN-1-YL]-(1H-PYRROLO-PYRIDIN-YL)-METHANONES AND SYNTHESIS THEREOF
  申请人：CHOI-SLEDESKI Yong Mi

  公开号：US20120245199A1

  公开（公告）日：2012-09-27

  The present invention relates herein to compounds and compositions for the treatment and amelioration of inflammatory disease. Specifically the present invention relates to compounds that having a tryptase inhibition activity and the intermediates thereof, pharmaceutical compositions comprising such compounds, and a method of treating subjects suffering from a condition disease or disorder that can be ameliorated by the administration of an inhibitor of tryptase.

  本发明涉及用于治疗和改善炎症性疾病的化合物和组合物。具体地，本发明涉及具有胰蛋白酶抑制活性及其中间体的化合物，包含这些化合物的药物组合物，以及治疗受试者病情、疾病或障碍的方法，该病情、疾病或障碍可以通过给予胰蛋白酶抑制剂而得到改善。
• DISUBSTITUTED [4-(5-AMINOMETHYL-PHENYL)-PIPERIDIN-1-YL]- 1H-INDOL-3-YL]-METHANONES
  申请人：CHOI-SLEDESKI Yong- Mi

  公开号：US20120142735A1

  公开（公告）日：2012-06-07

  The present invention extends to a compound of formula I: or a pharmaceutically acceptable salt of said compound, or a pharmaceutical composition comprising the compound of formula I and a pharmaceutically acceptable carrier. The invention is also directed to the use of a compound of formula I as an inhibitor of tryptase and for treating a patient suffering from, or subject to, a physiological condition in need of amelioration by an inhibitor of tryptase. The invention further includes methods for the preparation of a compound of formula I.

  本发明涉及式I的化合物：或该化合物的药学上可接受的盐，或包含式I的化合物和药学上可接受的载体的药物组合物。本发明还涉及使用式I的化合物作为组胺酶抑制剂，并用于治疗患有或受到需要组胺酶抑制剂改善的生理状况的患者。本发明还包括制备式I的化合物的方法。