4-(2-氯-6-氟苯基)哌啶盐酸盐 | 827017-15-2

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 哌啶类
• 中文名称: 4-(2-氯-6-氟苯基)哌啶盐酸盐
• 英文名称: 4-(2-chloro-6-fluoro-phenyl)-piperidine hydrochloride
• 英文别名: 4-(2-chloro-6-fluorophenyl)piperidine hydrochloride；4-(2-chloro-6-fluorophenyl)piperidine;hydrochloride
• CAS: 827017-15-2
• 化学式: C₁₁H₁₃ClFN*ClH
• 分子量: 250.143
• InChiKey: OFMGFJJFGLEERG-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.37
• 重原子数：
  15
• 可旋转键数：
  1
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.45
• 拓扑面积：
  12
• 氢给体数：
  2
• 氢受体数：
  2

反应信息

• 作为反应物：
  描述：

  4-(2-氯-6-氟苯基)哌啶盐酸盐 在 sodium hydride 、 溶剂黄146 、 N,N'-羰基二咪唑 作用下， 以 1,4-二氧六环 、 水 、 N,N-二甲基甲酰胺 、 乙腈 为溶剂， 反应 20.0h， 生成 [3-[4-(2-chloro-6-fluoro-phenyl)-piperidin-1-ylmethyl]-5-fluoro-2-(morpholine-4-carbonyl)-indol-1-yl]-acetic acid tert-butyl ester
  参考文献：
  名称：

  WO2008/818

  摘要：

  公开号：

文献信息

• [EN] SUBSTITUTED INDOLE LIGANDS FOR THE ORL-1 RECEPTOR<br/>[FR] LIGANDS D'INDOLE SUBSTITUES DESTINES UN RECEPTEUR ORL-1
  申请人：GLAXOSMITHKLINE SPA

  公开号：WO2005005411A1

  公开（公告）日：2005-01-20

  New ligands for the ORL-1 receptor are described, useful for modulating the activity of said receptors in a patient in need thereof, and for preventing and treating illnesses dependent on the stimulation of this receptor. The new compounds conform to structural formula (I), wherein Q is a moiety of formula (II) and R, R0, R1, R2, R3, R4, R5, R6 are further defined in the description.

  描述了用于调节ORL-1受体活性的新配体，适用于需要此类受体的患者，并用于预防和治疗依赖于该受体刺激的疾病。这些新化合物符合结构式（I），其中Q是式（II）的一个部分，而R、R0、R1、R2、R3、R4、R5、R6在描述中进一步定义。
• [EN] BENZOSUBERONYLPIPERIDINE COMPOUNDS AS ANALGESICS<br/>[FR] COMPOSES DE BENZOSUBERONYLPIPERIDINE COMME ANALGESIQUES
  申请人：SMITHKLINE BEECHAM SPA

  公开号：WO2001083454A1

  公开（公告）日：2001-11-08

  Compounds of formula (I) or a derivative thereof, wherein; R is C1-6alkyl, C3-7cycloalkyl, C1-6alkoxy, hydroxy, halo, C1-6alkenyl, C1-6alkynyl, amino, C1-6alkylamino, di(C1-6alkyl)amino, hydroxyC1-6alkyl, C1-6alkoxyC1-6alkyl, aminoC1-6alkyl, (C1-6alkyl)aminoC1-6alkyl, di(C1-6alkyl)aminoC1-6alkyl; R1 is hydrogen or R; R2 is hydroxy, C¿1-6?alkoxy, amino, C1-6alkylamino, di(C1-6alkyl)amino; R?3¿ is hydrogen or C¿1-6?alkyl; R?4 and R5¿ are each independently selected from the list consisting of perhaloC¿1-6?alkyl, hydrogen, halo, C1-6alkyl, C1-6alkoxy, hydroxy, amino, C1-6alkylamino, di(C1-6alkyl)amino, hydroxyC1-6alkyl, C1-6alkoxyC1-6alkyl, aminoC1-6alkyl, (C1-6alkyl)aminoC1-6alkyl, di(C1-6alkyl)aminoC1-6alkyl, aryl, and COX wherein X may be hydroxy, C1-6alkoxy, C1-6alkyl, amino, C1-6alkylamino, or di(C1-6alkyl)amino; with the proviso that, when R?3¿ is hydrogen, then R?4 and R5¿ are not both hydrogen; and wherein any alkyl group or the alkyl moiety of any group containing such a moiety may be substituted one or more times by halo; are ligands of the ORL-1 receptor and are useful in therapy.

  式(I)或其衍生物的化合物，其中：R为C1-6烷基，C3-7环烷基，C1-6烷氧基，羟基，卤素，C1-6烯基，C1-6炔基，氨基，C1-6烷基氨基，二（C1-6烷基）氨基，羟基C1-6烷基，C1-6烷氧基C1-6烷基，氨基C1-6烷基，（C1-6烷基）氨基C1-6烷基，二（C1-6烷基）氨基C1-6烷基；R1为氢或R；R2为羟基，C1-6烷氧基，氨基，C1-6烷基氨基，二（C1-6烷基）氨基；R3为氢或C1-6烷基；R4和R5各自独立地从以下列表中选择：全卤素C1-6烷基，氢，卤素，C1-6烷基，C1-6烷氧基，羟基，氨基，C1-6烷基氨基，二（C1-6烷基）氨基，羟基C1-6烷基，C1-6烷氧基C1-6烷基，氨基C1-6烷基，（C1-6烷基）氨基C1-6烷基，二（C1-6烷基）氨基C1-6烷基，芳基和COX，其中X可以是羟基，C1-6烷氧基，C1-6烷基，氨基，C1-6烷基氨基或二（C1-6烷基）氨基；但是，当R3为氢时，R4和R5不同时为氢；其中任何烷基或含有此类基团的任何基团的烷基部分均可被卤素取代一次或多次；是ORL-1受体的配体，并且在治疗中有用。
• Benzosuberonylpiperdine compounds as analgesics
  申请人：——

  公开号：US20040029917A1

  公开（公告）日：2004-02-12

  Compounds of formula (I) or a derivative thereof, wherein; R is C 1-6 allkyl, C 3-7 cycloalkyl, C 1-6 alkoxy, hydroxy, halo, C 1-6 alkenyl, C 1-6 allkynyl, amino, C 1-6 alkylamino, di(C 1-6 alkyl)amino, hydroxyC 1-6 alkyl, C 1-6 akoxyC 1-6 alkyl, aminoC 1-6 allkyl, (C 1-6 allkyl)aminoC 1-6 alkyl, di(C 1-6 allkyl)aminoC 1-6 alkyl; R 1 is hydrogen or R; R 2 is hydroxy, C 1-6 alkoxy, amino, C 1-6 alkylamino, di(C 1-6 alkyl)amino; R 3 is hydrogen or C 1-6 alkyl; R 4 and R 5 are each independently selected from the list consisting of perhaloC 1-6 alkyl, hydrogen, halo, C 1-6 alkyl, C 1-6 alkoxy, hydroxy, amino, C 1-6 akylamino, di(C 1-4 alkyl)amino, hydroxyC 1-6 alkyl, C 1-6 akoxyC 1-6 alkyl, aminoC 1-6 allkyl, (C 1-4 alkyl)aminoC 1-6 alkyl, di(C 1-4 alkyl)aminoC 1-4 alkyl, aryl, and COX wherein X may be hydroxy, C 1-6 alkoxy, C 1-6 alkyl, amino, C 1-6 alkylamino, or di(C 1-6 allkyl)amino; with the proviso that, when R 3 is hydrogen, then R R 4 and R 5 are not both hydrogen; and wherein any alkyl group or the alkyl moiety of any group containing such a moiety may be substituted one or more times by halo; are ligands of the ORL-1 receptor and are useful in therapy. 1

  式(I)或其衍生物的化合物，其中：R是C1-6烷基，C3-7环烷基，C1-6烷氧基，羟基，卤素，C1-6烯基，C1-6炔基，氨基，C1-6烷基氨基，二（C1-6烷基）氨基，羟基C1-6烷基，C1-6烷氧基C1-6烷基，氨基C1-6烷基，（C1-6烷基）氨基C1-6烷基，二（C1-6烷基）氨基C1-6烷基；R1是氢或R；R2是羟基，C1-6烷氧基，氨基，C1-6烷基氨基，二（C1-6烷基）氨基；R3是氢或C1-6烷基；R4和R5各自独立地选自以下列表中的物种：全卤素C1-6烷基，氢，卤素，C1-6烷基，C1-6烷氧基，羟基，氨基，C1-6烷基氨基，二（C1-4烷基）氨基，羟基C1-6烷基，C1-6烷氧基C1-6烷基，氨基C1-6烷基，（C1-4烷基）氨基C1-6烷基，二（C1-4烷基）氨基C1-4烷基，芳基，和COX，其中X可以是羟基，C1-6烷氧基，C1-6烷基，氨基，C1-6烷基氨基或二（C1-6烷基）氨基；但是，当R3是氢时，R、R4和R5不能同时为氢；其中任何烷基或含有此类基团的任何基团的烷基部分可以被卤素取代一次或多次；是ORL-1受体的配体，并且在治疗中有用。
• Substituted indole ligands for the orl-1 receptor
  申请人：Consonni Alessandra

  公开号：US20070197603A1

  公开（公告）日：2007-08-23

  New ligands for the ORL-1 receptor are described, useful for modulating the activity of said receptors in a patient in need thereof, and for preventing and treating illnesses dependent on the stimulation of this receptor. The new compounds conform to structural formula (I), wherein Q is a moiety of formula: and R, R 0 , R 1 , R 2 , R 3 , R 4 , R 5 , R 6 are further defined in the description.

  本文描述了ORL-1受体的新配体，可用于调节患者中该受体的活性，并用于预防和治疗依赖于该受体刺激的疾病。新化合物符合结构式（I），其中Q是以下式子的一个基团：而R，R0，R1，R2，R3，R4，R5，R6在描述中进一步定义。
• BENZOSUBERONYLPIPERIDINE COMPOUNDS AS ANALGESICS
  申请人：GlaxoSmithKline S.p.A.

  公开号：EP1278729A1

  公开（公告）日：2003-01-29