3-(2-fluorobenzyl)imidazo[1,5-a]pyridine-1-carbonitrile | 1011528-16-7

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 咪唑并吡啶类
• 英文名称: 3-(2-fluorobenzyl)imidazo[1,5-a]pyridine-1-carbonitrile
• 英文别名: 3-[(2-fluorophenyl)methyl]imidazo[1,5-a]pyridine-1-carbonitrile
• CAS: 1011528-16-7
• 化学式: C₁₅H₁₀FN₃
• 分子量: 251.263
• InChiKey: LNSKZAPAOQIRBH-UHFFFAOYSA-N

物化性质

• 密度：
  1.23±0.1 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  4
• 重原子数：
  19
• 可旋转键数：
  2
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.07
• 拓扑面积：
  41.1
• 氢给体数：
  0
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  3-(2-fluorobenzyl)imidazo[1,5-a]pyridine-1-carbonitrile 在 氯(甲基)铝酰胺 作用下， 以 甲苯 为溶剂， 反应 3.0h， 以90%的产率得到
  参考文献：
  名称：

  Soluble guanylate cyclase stimulators for the treatment of hypertension: Discovery of MK-2947

  摘要：

  The NO-sGC-cGMP signaling pathway plays an important role in the cardiovascular system. Loss of nitric oxide tone or impaired signaling has been associated with cardiovascular diseases, such as hypertension, pulmonary hypertension and heart failure. Direct activation of sGC enzyme independent of NO represents a novel approach for modulating NO signaling with tremendous therapeutic potential. Herein, we describe the design of a structurally novel class of heme-dependent sGC stimulators containing the 3,3-dimethylpyrrolidin-2-one moiety which resulted in the identification of the potent, selective stimulator 30 (MK-2947) for the treatment of hypertension.

  DOI：

  10.1016/j.bmcl.2020.127574
• 作为产物：
  描述：

  2-甲基氨基吡啶二盐酸盐 在 1,1'-双(二苯基膦)二茂铁 、 tris-(dibenzylideneacetone)dipalladium(0) 、 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 作用下， 以 二氯甲烷 、 N,N-二甲基甲酰胺 、 乙腈 为溶剂， 反应 22.5h， 生成 3-(2-fluorobenzyl)imidazo[1,5-a]pyridine-1-carbonitrile
  参考文献：
  名称：

  Soluble guanylate cyclase stimulators for the treatment of hypertension: Discovery of MK-2947

  摘要：

  The NO-sGC-cGMP signaling pathway plays an important role in the cardiovascular system. Loss of nitric oxide tone or impaired signaling has been associated with cardiovascular diseases, such as hypertension, pulmonary hypertension and heart failure. Direct activation of sGC enzyme independent of NO represents a novel approach for modulating NO signaling with tremendous therapeutic potential. Herein, we describe the design of a structurally novel class of heme-dependent sGC stimulators containing the 3,3-dimethylpyrrolidin-2-one moiety which resulted in the identification of the potent, selective stimulator 30 (MK-2947) for the treatment of hypertension.

  DOI：

  10.1016/j.bmcl.2020.127574

文献信息

• PYRAZOLOPYRIDINE, INDAZOLE, IMIDAZOPYRIDINE, IMIDAZOPYRIMIDINE, PYRAZOLOPYRAZINE AND PYRAZOLOPYRIDINE DERIVATIVES AS STIMULATORS OF GUANYLATE CYCLASE FOR CARDIOVASCULAR DISORDERS
  申请人：Schirok Hartmut

  公开号：US20100029653A1

  公开（公告）日：2010-02-04

  The present application relates to novel azabicyclic compounds, processes for their preparation, their use alone or in combinations for the treatment and/or prevention of diseases, and their use for producing medicaments for the treatment and/or prevention of diseases, especially for the treatment and/or prevention of cardiovascular disorders.

  本申请涉及新型氮杂双环化合物，其制备方法，它们单独或与其他物质结合用于治疗和/或预防疾病，以及用于生产治疗和/或预防疾病的药物，特别是用于治疗和/或预防心血管疾病。
• Pyrazolopyridine, indazole, imidazopyridine, imidazopyrimidine, pyrazolopyrazine and pyrazolopyridine derivatives as stimulators of guanylate cyclase for cardiovascular disorders
  申请人：Bayer Intellectual Property GmbH

  公开号：US08309551B2

  公开（公告）日：2012-11-13

  The present application relates to novel azabicyclic compounds, processes for their preparation, their use alone or in combinations for the treatment and/or prevention of diseases, and their use for producing medicaments for the treatment and/or prevention of diseases, especially for the treatment and/or prevention of cardiovascular disorders.

  本申请涉及新型杂环双环化合物、其制备过程，它们单独或组合使用用于治疗和/或预防疾病，以及它们用于制造治疗和/或预防疾病的药物，特别是用于治疗和/或预防心血管疾病。
• Acidic triazoles as soluble guanylate cyclase stimulators
  作者：Lee R. Roberts、Paul A. Bradley、Mark E. Bunnage、Katherine S. England、David Fairman、Yvette M. Fobian、David N.A. Fox、Geoff E. Gymer、Steven E. Heasley、Jerome Molette、Graham L. Smith、Michelle A. Schmidt、Michael A. Tones、Kevin N. Dack

  DOI：10.1016/j.bmcl.2011.08.071

  日期：2011.11

  A series of acidic triazoles with activity as soluble guanylate cyclase stimulators is described. Incorporation of the CF(3) triazole improved the overall physicochemical and drug-like properties of the molecule and is exemplified by compound 25. (C) 2011 Elsevier Ltd. All rights reserved.
• US8309551B2
  申请人：——

  公开号：US8309551B2

  公开（公告）日：2012-11-13
• [DE] PYRAZOLOPYRIDIN, INDAZOL, IMIDAZOPYRIDIN, IMIDAZOPYRIMIDIN, PYRAZOLOPYRAZIN UND PYRAZOLOPYRIDIN DERIVATE ALS STIMULATOREN DER GUANYLATCYCLASE ZUR HERZ-KREISLAUFERKRANKUNGEN<br/>[EN] PYRAZOLOPYRIDINE, INDAZOLE, IMIDAZOPYRIDINE, IMIDAZOPYRIMIDINE, PYRAZOLOPYRAZINE AND PYRAZOLOPYRIDINE DERIVATES AS STIMULATORS OF GUANYLATE CYCLASE FOR CARDIOVASCULAR DISORDERS<br/>[FR] DÉRIVÉ DE PYRAZOLOPYRIDINE, INDAZOLE, IMIDAZOPYRIDINE, IMIDAZOPYRIMIDINE, PYRAZOLOPYRAZINE ET PYRAZOLOPYRIDINE EN TANT QUE STIMULANT DE LA GUANYLATCYCLASE POUR LES MALADIES CARDIOVASCULAIRES
  申请人：BAYER HEALTHCARE AG

  公开号：WO2008031513A1

  公开（公告）日：2008-03-20

  [EN] The present application relates to compounds of the formula (I) which act as stimulators of soluble guanylate cyclase and to their use for treatment and/or prevention of heart failure, angina pectoris, hypertension, pulmonary hypertension, ischaemias, vascular disorders, thromboembolic disorders and arteriosclerosis. L-CH₂-M-Q (I) in which L is phenyl, pyridyl, furyl, thienyl, thiazolyl, oxazolyl, isothiazolyl, isoxazolyl or (C₅-C₇)-cycloalkyl, M is a bicyclic heteroaryl group of the formula (a-1), (b-1) or (c-1), in which the attachment site to the group is -CH₂-L, the attachment site to the group is Q, and A, B, D and E are each CH, CR¹ or N, where not more than two of the ring members A, B, D and E are the same, and Q is an unsaturated or aromatic 5- or 6-membered heterocycle having up to four heteroatoms from the group of N, O and/or S.
  [FR] La présente invention concerne un composé de formule (I), qui agit en tant que stimulant de la guanylatcyclase soluble et son utilisation pour le traitement et/ou la prévention de l'insuffisance cardiaque, de l'angine de poitrine, de l'hypertonie, de l'hypertonie pulmonaire, de l'ischémie, des angiopathies, des maladies thromboemboliques et de l'artériosclérose. L-CH₂-M-Q (I) dans laquelle L représente phényle, pyridyle, furyle, thiényle, thiazolyle, oxazolyle, isothiazolyle, isoxazolyle ou un cycloalkyle en (C₅-C₇), M représente un groupement hétéroaryle de formule (a-1), (b-1) ou (c-1), le site de liaison représentant le groupement -CH₂-L, le site de liaison représentant le groupement Q, A, B, D et E représentant chacun CH, CR¹ ou N. Selon l'invention, au plus deux des éléments cycliques A, B, D et E sont identiques et Q représente un hétérocycle insaturé ou aromatique ayant 5 ou 6 éléments, avec jusqu'à quatre hétéroatomes de la série N, O et/ou S.
  [DE] Die vorliegende Anmeldung betrifft Verbindung der Formel (I), die als Simulatoren der löslichen Guanylatcyclase wirken und ihre Verwendung zur Behandlung und/oder Prävention von Herzinsuffizienz, Angina pectoris, Hypertonie, pulmonaler Hypertonie, Ischämien, Gefässerkrankungen, thromboembolischen Erkrankungen und Arteriosklerose. L-CH₂-M-Q (I) in welcher L für Phenyl, Pyridyl, Furyl, Thienyl, Thiazolyl, Oxazolyl, Isothiazolyl, Isoxazolyl oder (C₅-C₇)-Cycloalkyl, M für eine bicyclische Heteroaryl-Gruppe der Formel (a-1), (b-1) oder (c-1) steht, worin die Verknüpfungsstelle mit der Gruppe -CH₂-L bedeutet, die Verknüpfungsstelle mit der Gruppe Q bedeutet, A, B, D und E jeweils CH, CR¹ oder N bedeuten, wobei maximal zwei der Ringglieder A, B, D und E zugleich stehen, und Q für einen ungesättigten oder aromatischen 5- oder 6-gliedrigen Heterocyclus mit bis zu vier Heteroatomen aus der Reihe N1 O und/oder S steht.