(R)-1-(6-methoxypyridin-3-yl)propylamine | 767351-04-2

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: (R)-1-(6-methoxypyridin-3-yl)propylamine
• 英文别名: 1(R)-(6-methoxypyridin-3-yl)propylamine；(R)-1-(6-Methoxypyridin-3-yl)propan-1-amine；(1R)-1-(6-methoxypyridin-3-yl)propan-1-amine
• CAS: 767351-04-2
• 化学式: C₉H₁₄N₂O
• 分子量: 166.223
• InChiKey: QHQMNKOGFJRYTE-MRVPVSSYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  0.9
• 重原子数：
  12
• 可旋转键数：
  3
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.44
• 拓扑面积：
  48.1
• 氢给体数：
  1
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  (R)-1-(6-methoxypyridin-3-yl)propylamine 、 8-((R)-1-phenylpropylcarbamoyl)-3,4-dihydro-1H-pyrrolo[2,1-c][1,4]oxazine-6-carboxylic acid 在 1-羟基苯并三唑 、 盐酸-N-乙基-Nˊ-(3-二甲氨基丙基)碳二亚胺 作用下， 以 N,N-二甲基甲酰胺 为溶剂， 反应 2.67h， 以78%的产率得到3,4-dihydro-1H-pyrrolo[2,1-c][1,4]oxazine-6,8-dicarboxylic acid 6-{[(R)-1-(6-methoxypyridin-3-yl)propyl]amide} 8-[((R)-1-phenylpropyl)amide]
  参考文献：
  名称：

  [EN] FUSED PYRROLEDICARBOXAMIDES AND THEIR USE AS PHARMACEUTICALS
  [FR] PYRROLEDICARBOXAMIDES FUSIONNÉS ET LEUR UTILISATION EN TANT QUE PRODUITS PHARMACEUTIQUES

  摘要：

  本发明涉及公式（I）中的融合吡咯二羧酰胺，其中R1至R9、X、m和n如权利要求中所定义。公式（I）化合物是酸敏感钾通道TASK-1的抑制剂，适用于治疗TASK-1通道介导的疾病，如心律失常，特别是心房心律失常，如心房颤动或心房扑动，以及呼吸系统疾病，特别是与睡眠相关的呼吸系统疾病，如睡眠呼吸暂停症等。

  公开号：

  WO2013113860A1
• 作为产物：
  描述：

  1-(6-methoxypyridin-3-yl)propan-1-amine 生成 (R)-1-(6-methoxypyridin-3-yl)propylamine 、 1(S)-(6-methoxypyridin-3-yl)propylamine
  参考文献：
  名称：

  2-(Butyl-1-sulfonylamino)-N-[1(R)-(6-methoxypyridin-3-yl)propyl] benzamide, its use as a medicament, and pharmaceutical preparations comprising it

  摘要：

  该发明涉及化合物2-(丁基-1-磺酰氨基)-N-[1(R)-(6-甲氧基吡啶-3-基)丙基]苯甲酰胺（化学式I1）及其药用可接受的盐，它们的制备和用途，特别用于治疗和预防心房心律失常，例如心房颤动或心房扑动。

  公开号：

  US20040192738A1

文献信息

• SUBSTITUTED 2-(CHROMAN-6-YLOXY)-THIAZOLES AND THEIR USE AS PHARMACEUTICALS
  申请人：CZECHTIZKY Werngard

  公开号：US20130065859A1

  公开（公告）日：2013-03-14

  The present invention relates to substituted 2-(chroman-6-yloxy)-thiazoles of the formula I, in which Ar, R2, R3 and R4 are as defined in the claims. The compounds of the formula I are inhibitors of the sodium-calcium exchanger (NCX), especially of the sodium-calcium exchanger of subtype 1 (NCX1), and are suitable for the treatment of diverse disorders in which intracellular calcium homeostasis is disturbed, such as arrhythmias, heart failure and stroke. The invention furthermore relates to processes for the preparation of the compounds of the formula I, their use as pharmaceuticals, and pharmaceutical compositions comprising them.

  本发明涉及式I的取代2-(色甘醇-6-氧基)-噻唑衍生物，其中Ar、R2、R3和R4如权利要求中所定义。式I的化合物是钠-钙交换蛋白（NCX）的抑制剂，特别是亚型1的钠-钙交换蛋白（NCX1），适用于处理细胞内钙离子稳态受扰的各种疾病，如心律失常、心力衰竭和中风。本发明还涉及制备式I的化合物的方法，它们作为药物的用途，以及包含它们的药物组合物。
• SULFONYLAMINOBENZOIC ACID AND SALT
  申请人：Brendel Joachim

  公开号：US20080081926A1

  公开（公告）日：2008-04-03

  The invention relates to a compound selected from the group consisting of which is suitable for use in the synthesis of 2-(butyl-1-sulfonylamino)-N-[1(R)-(6-methoxypyridin-3-yl)propyl]benzamide.

  本发明涉及一种化合物，选自以下组合物，适用于2-(丁基-1-磺酰氨基)-N-[1(R)-(6-甲氧基吡啶-3-基)丙基]苯甲酰胺的合成。
• SUBSITUTED 2-(CHROMAN-6-YLOXYL)-THIAZOLES AND THEIR USE AS PHARMACEUTICALS
  申请人：Sanofi

  公开号：US20140243292A1

  公开（公告）日：2014-08-28

  The present invention relates to substituted 2-(chroman-6-yloxy)-thiazoles of the formula I, in which Ar, R2, R3 and R4 are as defined in the claims. The compounds of the formula I are inhibitors of the sodium-calcium exchanger (NCX), especially of the sodium-calcium exchanger of subtype 1 (NCX1), and are suitable for the treatment of diverse disorders in which intracellular calcium homeostasis is disturbed, such as arrhythmias, heart failure and stroke. The invention furthermore relates to processes for the preparation of the compounds of the formula I, their use as pharmaceuticals, and pharmaceutical compositions comprising them.

  本发明涉及式I的取代2-(色烯-6-氧基)-噻唑，其中Ar，R2，R3和R4如权利要求所定义。公式I化合物是钠钙交换器（NCX）的抑制剂，特别是钠钙交换器亚型1（NCX1）的抑制剂，并适用于治疗细胞内钙离子稳态受到干扰的多种疾病，如心律失常，心力衰竭和中风。本发明还涉及制备公式I化合物的方法，它们作为药物的用途，以及包含它们的制药组合物。
• 2-(Butyl-1-sulfonylamino)-n-[1(R)-(6-methoxy-pyridin-3-yl)-propyl]-benzamid, the use thereof in the form of drug an pharmaceutical preparations containing said compound
  申请人：BRENDEL Joachim

  公开号：US20090209767A1

  公开（公告）日：2009-08-20

  The invention relates to 2-(butyl-1-sulfonylamino)-N-[1(R)-(6-methoxy-pyridin-3-yl)propyl]benzamide of the formula I and to its pharmaceutically acceptable salts, their preparation and use, in particular for the treatment and prophylaxis of atrial arrhythmias, for example atrial fibrillation or atrial flutters.

  该发明涉及公式I的2-(丁基-1-磺酰氨基)-N-[1(R)-(6-甲氧基-吡啶-3-基)丙基]苯甲酰胺及其药学上可接受的盐，它们的制备和用途，特别是用于治疗和预防心房心律失常，例如心房颤动或心房扑动。
• Fused Pyrroledicarboxamides and Their Use as Pharmaceuticals
  申请人：SANOFI

  公开号：US20160159793A1

  公开（公告）日：2016-06-09

  The present invention relates in fused pyrroledicarboxamides of the formula (I), in which R1 to R9, X, m and n are as defined in claims. The compounds of the formula (I) are inhibitors of the acid-sensitive potassium channel TASK-1 and suitable for the treatment of TASK-1 channel-mediated diseases such as arrhythmias, in particular atrial arrhythmias like atrial fibrillation or atrial flutter, and respiratory disorders, in particular sleep-related respiratory disorders like sleep apnea, for example.

  本发明涉及式(I)的融合吡咯二酰胺，其中R1至R9、X、m和n如权利要求中所定义。公式(I)化合物是酸敏感钾通道TASK-1的抑制剂，适用于治疗TASK-1通道介导的疾病，如心律失常，特别是房颤或心房扑动，以及呼吸系统疾病，特别是睡眠相关呼吸障碍，如睡眠呼吸暂停等。