4-({(1S,2R)-5,5-difluoro-2-[1-(4-methoxybenzyl)-1H-pyrazol-4-yl]cyclohexyl}oxy)-N-(2,4-dimethoxybenzyl)-2-fluoro-5-methyl-N-(pyrimidin-4-yl)benzenesulfonamide | 1450599-27-5

• 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: 4-({(1S,2R)-5,5-difluoro-2-[1-(4-methoxybenzyl)-1H-pyrazol-4-yl]cyclohexyl}oxy)-N-(2,4-dimethoxybenzyl)-2-fluoro-5-methyl-N-(pyrimidin-4-yl)benzenesulfonamide
• 英文别名: 4-({(1S*,2R*)-5,5-difluoro-2-[1-(4-methoxybenzyl)-1H-pyrazol-4-yl]cyclohexyl}oxy)-N-(2,4-dimethoxybenzyl)-2-fluoro-5-methyl-N-(pyrimidin-4-yl)benzenesulfonamide；4-[(1S,2R)-5,5-difluoro-2-[1-[(4-methoxyphenyl)methyl]pyrazol-4-yl]cyclohexyl]oxy-N-[(2,4-dimethoxyphenyl)methyl]-2-fluoro-5-methyl-N-pyrimidin-4-ylbenzenesulfonamide
• CAS: 1450599-27-5
• 化学式: C₃₇H₃₈F₃N₅O₆S
• 分子量: 737.8
• InChiKey: XWINRYJBHMKKLR-HKFHRXRESA-N

计算性质

• 辛醇/水分配系数(LogP)：
  6.3
• 重原子数：
  52
• 可旋转键数：
  13
• 环数：
  6.0
• sp3杂化的碳原子比例：
  0.32
• 拓扑面积：
  126
• 氢给体数：
  0
• 氢受体数：
  13

反应信息

• 作为反应物：
  描述：

  4-({(1S,2R)-5,5-difluoro-2-[1-(4-methoxybenzyl)-1H-pyrazol-4-yl]cyclohexyl}oxy)-N-(2,4-dimethoxybenzyl)-2-fluoro-5-methyl-N-(pyrimidin-4-yl)benzenesulfonamide 在 三乙基硅烷 、 三氟乙酸 作用下， 以 二氯甲烷 为溶剂， 反应 1.0h， 以94%的产率得到4-{[(1S,2R)-5,5-difluoro-2-(1H-pyrazol-4-yl)cyclohexyl]oxy}-2-fluoro-5-methyl-N-(pyrimidin-4-yl)benzenesulfonamide
  参考文献：
  名称：

  호흡기 질환용 약

  摘要：

  这段文字是关于药物化学的内容，描述了用于治疗呼吸道疾病或钠通道相关疾病的药物的有效成分。由于内容较为专业和复杂，建议您咨询专业医学人士或药剂师以获取更详细的解释和信息。

  公开号：

  KR20150126620A

文献信息

• Cycloalkane Derivatives
  申请人：Daiichi Sankyo Company, Limited

  公开号：US20140045862A1

  公开（公告）日：2014-02-13

  Disclosed herein are therapeutic agents and/or preventive agents for pain or therapeutic agents and/or preventive agents for a sodium channel associated disease. The present invention provides compounds represented by the following formula (I) or pharmacologically acceptable salts thereof:

  本文揭示了用于疼痛的治疗剂和/或预防剂，或者用于钠通道相关疾病的治疗剂和/或预防剂。本发明提供以下式（I）所代表的化合物或其药理学上可接受的盐：
• Cycloalkane derivatives
  申请人：Daiichi Sankyo Company, Limited

  公开号：US08889741B2

  公开（公告）日：2014-11-18

  Disclosed herein are therapeutic agents and/or preventive agents for pain or therapeutic agents and/or preventive agents for a sodium channel associated disease. The present invention provides compounds represented by the following formula (I) or pharmacologically acceptable salts thereof:

  本文披露了用于疼痛的治疗剂和/或预防剂，或用于钠通道相关疾病的治疗剂和/或预防剂。本发明提供以下公式（I）所代表的化合物或其药理学上可接受的盐：
• CYCLOALKANE DERIVATIVES
  申请人：Daiichi Sankyo Company, Limited

  公开号：US20150018551A1

  公开（公告）日：2015-01-15

  Disclosed herein are therapeutic agents and/or preventive agents for pain or therapeutic agents and/or preventive agents for a sodium channel associated disease. The present invention provides compounds represented by the following formula (I) or pharmacologically acceptable salts thereof:

  本文公开了治疗或预防疼痛的治疗剂和/或预防剂，或与钠通道相关疾病的治疗剂和/或预防剂。本发明提供以下公式（I）所代表的化合物或其药学上可接受的盐：
• DRUG FOR RESPIRATORY DISEASES
  申请人：DAIICHI SANKYO COMPANY, LIMITED

  公开号：US20160038486A1

  公开（公告）日：2016-02-11

  It is intended to provide a therapeutic agent and/or a preventive agent for a respiratory disease or a therapeutic agent and/or a preventive agent for a sodium channel associated disease. The present invention provides a pharmaceutical comprising a compound represented by the following formula (I) or a pharmacologically acceptable salt thereof as an active ingredient: Ar 1 and Ar 2 : a heteroaryl group or an aryl group; R 1 , R 2 and R 3 : a hydrogen atom, a halogen atom, a C1-C6 alkyl group, a halogenated C1-C6 alkyl group, a hydroxy C1-C6 alkyl group, a C1-C6 alkoxy C1-C6 alkyl group or a C3-C7 cycloalkyl group or a cyano group; R 4 and R 5 : a hydrogen atom, a halogen atom, a C1-C6 alkyl group, a halogenated C1-C6 alkyl group, a hydroxyl group, a hydroxy C1-C6 alkyl group, a C1-C6 alkoxy C1-C6 alkyl group, a C3-C7 cycloalkyl group or a C1-C6 alkoxy group; n: an integer of 1 to 3; and the heteroaryl or aryl group optionally has one or two groups independently selected from a halogen atom, a C1-C6 alkyl group, a halogenated C1-C6 alkyl group, a hydroxyl group, a hydroxy C1-C6 alkyl group, a C1-C6 alkoxy C1-C6 alkyl group, a C3-C7 cycloalkyl group, a carboxyl group, a cyano group, an amino group, a C1-C3 alkylamino group and a di-C1-C3 alkylamino group, and when the heteroaryl or aryl group has two such groups, the two groups are the same as or different from each other.

  本发明旨在提供一种治疗剂和/或预防剂，用于呼吸系统疾病或钠通道相关疾病的治疗剂和/或预防剂。本发明提供一种药物，其中包含以下式（I）表示的化合物或其药理学上可接受的盐作为活性成分：Ar1和Ar2：杂环芳基或芳基；R1，R2和R3：氢原子，卤素原子，C1-C6烷基，卤代C1-C6烷基，羟基C1-C6烷基，C1-C6烷氧基C1-C6烷基或C3-C7环烷基或氰基；R4和R5：氢原子，卤素原子，C1-C6烷基，卤代C1-C6烷基，羟基，羟基C1-C6烷基，C1-C6烷氧基C1-C6烷基，C3-C7环烷基或C1-C6烷氧基；n：1到3的整数；杂环芳基或芳基可以选择具有一个或两个独立选择的基团，包括卤素原子，C1-C6烷基，卤代C1-C6烷基，羟基，羟基C1-C6烷基，C1-C6烷氧基C1-C6烷基，C3-C7环烷基，羧基，氰基，氨基，C1-C3烷基氨基和二C1-C3烷基氨基，当杂环芳基或芳基具有两个这样的基团时，这两个基团相同或不同。
• CYCLOALKANE DERIVATIVE
  申请人：Daiichi Sankyo Co., Ltd.

  公开号：EP2813491A1

  公开（公告）日：2014-12-17

  It is intended to provide a therapeutic agent and/or a preventive agent for pain or a therapeutic agent and/or a preventive agent for a sodium channel associated disease. The present invention provides a compound represented by the following formula (I) or a pharmacologically acceptable salt thereof: Ar1 and Ar2: a heteroaryl group or an aryl group; R1, R2 and R3: a hydrogen atom, a halogen atom, a C1-C6 alkyl group, a halogenated C1-C6 alkyl group, a hydroxy C1-C6 alkyl group, a C1-C6 alkoxy C1-C6 alkyl group or a C3-C7 cycloalkyl group or a cyano group; R4 and R5: a hydrogen atom, a halogen atom, a C1-C6 alkyl group, a halogenated C1-C6 alkyl group, a hydroxyl group, a hydroxy C1-C6 alkyl group, a C1-C6 alkoxy C1-C6 alkyl group, a C3-C7 cycloalkyl group or a C1-C6 alkoxy group; n: an integer of 1 to 3; and the heteroaryl group or the aryl group optionally has one or two groups independently selected from a halogen atom, a C1-C6 alkyl group, a halogenated C1-C6 alkyl group, a hydroxyl group, a hydroxy C1-C6 alkyl group, a C1-C6 alkoxy C1-C6 alkyl group, a C3-C7 cycloalkyl group, a carboxyl group, a cyano group, an amino group, a C1-C3 alkylamino group and a di-Cl-C3 alkylamino group, and when the heteroaryl group or the aryl group has two such groups, the two groups are the same as or different from each other.

  本发明旨在提供一种疼痛治疗剂和/或预防剂，或一种钠通道相关疾病的治疗剂和/或预防剂。本发明提供了由下式（I）代表的化合物或其药理学上可接受的盐： Ar1和Ar2：杂芳基或芳基； R1、R2和R3：氢原子、卤素原子、C1-C6烷基、卤代C1-C6烷基、羟基C1-C6烷基、C1-C6烷氧基C1-C6烷基或C3-C7环烷基或氰基； R4和R5：氢原子、卤素原子、C1-C6 烷基、卤代 C1-C6 烷基、羟基、羟基 C1-C6 烷基、C1-C6 烷氧基 C1-C6 烷基、C3-C7 环烷基或 C1-C6 烷氧基； n：1 至 3 的整数；以及 杂芳基或芳基任选具有一个或两个独立选自卤素原子、C1-C6 烷基、卤代 C1-C6 烷基、羟基、羟基 C1-C6 烷基、C1-C6 烷氧基 C1-C6 烷基、C3-C7 环烷基、羧基、氰基、氨基、C1-C3 烷基氨基和二-C3 烷基氨基的基团，当杂芳基或芳基具有两个此类基团时，这两个基团彼此相同或不同。