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4-(Piperidin-3-yl)aniline hydrochloride | 19733-57-4

中文名称
——
中文别名
——
英文名称
4-(Piperidin-3-yl)aniline hydrochloride
英文别名
4-piperidin-3-ylaniline;hydrochloride
4-(Piperidin-3-yl)aniline hydrochloride化学式
CAS
19733-57-4
化学式
C11H17ClN2
mdl
——
分子量
212.72
InChiKey
FNBFLNPVBYZZQT-UHFFFAOYSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

物化性质

  • 熔点:
    225-227 °C

计算性质

  • 辛醇/水分配系数(LogP):
    2.16
  • 重原子数:
    14
  • 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:
    38
  • 氢给体数:
    3
  • 氢受体数:
    2

安全信息

  • 海关编码:
    2933399090

文献信息

  • [EN] PYRAZOLE CARBOXAMIDE DERIVATIVES AS TAAR MODULATORS FOR USE IN THE TREATMENT OF SEVERAL DISORDERS, SUCH AS DEPRESSION, DIABETES AND PARKINSON'S DISEASE<br/>[FR] DÉRIVÉS DE PYRAZOLE-CARBOXAMIDE EN TANT QUE MODULATEURS DE TAAR POUR UTILISATION DANS LE TRAITEMENT DE PLUSIEURS TROUBLES, TELS QUE LA DÉPRESSION, LE DIABÈTE ET LA MALADIE DE PARKINSON
    申请人:HOFFMANN LA ROCHE
    公开号:WO2014041007A1
    公开(公告)日:2014-03-20
    The present invention relates to compounds of formula (I) wherein R1 is phenyl, optionally substituted by halogen, lower alkyl, lower cycloalkyl, lower alkoxy, cyano, lower alkyl substituted by halogen, lower alkyl substituted by hydroxy, lower alkoxy substituted by halogen or lower alkoxy substituted by hydroxy; or is pyridine-2, 3 or 4-yl, optionally substituted by halogen, lower alkyl, lower cycloalkyl, cyano, lower alkyl substituted by halogen, lower alkyl substituted by hydroxy, lower alkoxy, lower alkoxy substituted by halogen or lower alkoxy substituted by hydroxyl; or is pyrimidin-2, 4 or 5-yl, optionally substituted by halogen, lower alkyl, lower cycloalkyl, lower alkyl substituted by hydroxy or lower alkyl substituted by halogen; or is pyrazin-2-yl, optionally substituted by halogen, lower alkyl, lower cycloalkyl, lower alkyl substituted by halogen, lower alkyl substituted by hydroxy or cyano; or is 2,2-difluorobenzo[d][l,3]dioxol-5-yl, or is thiazolyl, optionally substituted by lower alkyl substituted by halogen; R2 is hydrogen or lower alkyl; R3 is hydrogen, amino or lower alkyl; Z is a bond, -CH2- or -O-; or to a pharmaceutically suitable acid addition salt thereof. It has now been found that the compounds of formulas I have a good affinity to the trace amine associated receptors (TAARs), especially for TAAR1. The compounds may be used for the treatment of depression, anxiety disorders, bipolar disorder, attention deficit hyperactivity disorder (ADHD), stress-related disorders, psychotic disorders such as schizophrenia, neurological diseases such as Parkinson's disease, neurodegenerative disorders such as Alzheimer's disease, epilepsy, migraine, hypertension, substance abuse and metabolic disorders such as eating disorders, diabetes, diabetic complications, obesity, dyslipidemia, disorders of energy consumption and assimilation, disorders and malfunction of body temperature homeostasis, disorders of sleep and circadian rhythm, and cardiovascular disorders.
    本发明涉及以下式(I)的化合物,其中R1是苯基,可以被卤素、较低烷基、较低环烷基、较低烷氧基、基、被卤素取代的较低烷基、被羟基取代的较低烷基、被卤素取代的较低烷氧基或被羟基取代的较低烷氧基;或是吡啶-2、3或4-基,可以被卤素、较低烷基、较低环烷基、基、被卤素取代的较低烷基、被羟基取代的较低烷基、较低烷氧基、被卤素取代的较低烷氧基或被羟基取代的较低烷氧基取代;或是嘧啶-2、4或5-基,可以被卤素、较低烷基、较低环烷基、被羟基取代的较低烷基或被卤素取代的较低烷基取代;或是吡嗪-2-基,可以被卤素、较低烷基、较低环烷基、被卤素取代的较低烷基、被羟基取代的较低烷基或基取代;或是2,2-二氟苯并[d][1,3]二氧杂环-5-基,或是噻唑基,可以被被卤素取代的较低烷基取代;R2是氢或较低烷基;R3是氢、基或较低烷基;Z是键,-CH2-或-O-;或其药学上适用的酸盐。现已发现,式I的化合物对追踪胺相关受体(TAARs)有很好的亲和力,尤其是对TAAR1。这些化合物可用于治疗抑郁症、焦虑症、双相情感障碍、注意力缺陷多动障碍(ADHD)、与压力相关的障碍、精神分裂症等精神障碍、帕森病等神经系统疾病、阿尔茨海默病等神经退行性疾病、癫痫、偏头痛、高血压、物质滥用以及代谢障碍,如进食障碍、糖尿病、糖尿病并发症、肥胖症、血脂异常、能量消耗和吸收障碍、体温稳态障碍、睡眠和昼夜节律障碍,以及心血管疾病。
  • PYRAZOLE CARBOXAMIDE COMPOUNDS AND USES THEREOF
    申请人:Hoffmann-La Roche Inc.
    公开号:US20150218131A1
    公开(公告)日:2015-08-06
    The present invention relates to compounds of formula wherein R 1 is phenyl, optionally substituted by halogen, lower alkyl, lower cycloalkyl, lower alkoxy, cyano, lower alkyl substituted by halogen, lower alkyl substituted by hydroxy, lower alkoxy substituted by halogen or lower alkoxy substituted by hydroxy; or is pyridine-2, 3 or 4-yl, optionally substituted by halogen, lower alkyl, lower cycloalkyl, cyano, lower alkyl substituted by halogen, lower alkyl substituted by hydroxy, lower alkoxy, lower alkoxy substituted by halogen or lower alkoxy substituted by hydroxyl; or is pyrimidin-2, 4 or 5-yl, optionally substituted by halogen, lower alkyl, lower cycloalkyl, lower alkyl substituted by hydroxy or lower alkyl substituted by halogen; or is pyrazin-2-yl, optionally substituted by halogen, lower alkyl, lower cycloalkyl, lower alkyl substituted by halogen, lower alkyl substituted by hydroxy or cyano; or is 2,2-difluorobenzo[d][1,3]dioxol-5-yl, or is thiazolyl, optionally substituted by lower alkyl substituted by halogen; R 2 is hydrogen or lower alkyl; R 3 is hydrogen, amino or lower alkyl; Z is a bond, —CH 2 — or —O—; or to a pharmaceutically suitable acid addition salt thereof. It has now been found that the compounds of formulas I have a good affinity to the trace amine associated receptors (TAARs), especially for TAAR1. The compounds may be used for the treatment of depression, anxiety disorders, bipolar disorder, attention deficit hyperactivity disorder (ADHD), stress-related disorders, psychotic disorders such as schizophrenia, neurological diseases such as Parkinson's disease, neurodegenerative disorders such as Alzheimer's disease, epilepsy, migraine, hypertension, substance abuse and metabolic disorders such as eating disorders, diabetes, diabetic complications, obesity, dyslipidemia, disorders of energy consumption and assimilation, disorders and malfunction of body temperature homeostasis, disorders of sleep and circadian rhythm, and cardiovascular disorders.
    本发明涉及以下式的化合物: 其中, R1是苯基,可以被卤素、低烷基、低环烷基、低烷氧基、基、被卤素取代的低烷基、被羟基取代的低烷基、被卤素取代的低烷氧基或被羟基取代的低烷氧基;或是吡啶-2、3或4-基,可以被卤素、低烷基、低环烷基、基、被卤素取代的低烷基、被羟基取代的低烷基、低烷氧基、被卤素取代的低烷氧基或被羟基取代的低烷氧基取代; 或是嘧啶-2、4或5-基,可以被卤素、低烷基、低环烷基、被羟基取代的低烷基或被卤素取代的低烷基取代; 或是吡唑-2-基,可以被卤素、低烷基、低环烷基、被卤素取代的低烷基、被羟基取代的低烷基或基取代; 或是2,2-二氟苯并[d][1,3]二氧杂环-5-基; 或是噻唑基,可以被被卤素取代的低烷基取代; R2是氢或低烷基; R3是氢、基或低烷基; Z是键,-CH2-或-O-; 或是其药学上适宜的酸盐。 现已发现,式I的化合物对微量胺基关联受体(TAARs)具有良好的亲和力,尤其是对TAAR1。 该化合物可用于治疗抑郁症、焦虑症、双相情感障碍、注意力缺陷多动障碍(ADHD)、压力相关障碍、精神疾病如精神分裂症、神经疾病如帕森病、神经退行性疾病如阿尔茨海默病、癫痫、偏头痛、高血压、物质滥用和代谢性疾病如进食障碍、糖尿病、糖尿病并发症、肥胖症、血脂异常、能量消耗和吸收障碍、体温稳态障碍、睡眠和昼夜节律障碍以及心血管疾病的治疗。
  • SUBSTITUTED BENZAMIDES
    申请人:Hoffmann-La Roche Inc.
    公开号:US20160264596A1
    公开(公告)日:2016-09-15
    The invention relates to compounds of formula wherein R, R 1 , R 2 , X, and Y are as defined herein and to a pharmaceutically suitable acid addition salt thereof. Compounds of formula I have a good affinity to the trace amine associated receptors (TAARs), especially for TAAR1. The compounds can be used for the treatment of depression, anxiety disorders, bipolar disorder, attention deficit hyperactivity disorder (ADHD), stress-related disorders, psychotic disorders such as schizophrenia, neurological diseases such as Parkinson's disease, neurodegenerative disorders such as Alzheimer's disease, epilepsy, migraine, hypertension, substance abuse and metabolic disorders such as eating disorders, diabetes, diabetic complications, obesity, dyslipidemia, disorders of energy consumption and assimilation, disorders and malfunction of body temperature homeostasis, disorders of sleep and circadian rhythm, and cardiovascular disorders.
    本发明涉及以下式的化合物,其中R,R1,R2,X和Y如本文所定义,以及其药物适宜性酸盐。公式I的化合物对痕量胺相关受体(TAARs)具有良好的亲和力,尤其是对TAAR1。这些化合物可用于治疗抑郁症,焦虑症,双相情感障碍,注意力缺陷多动障碍(ADHD),与压力相关的障碍,精神疾病如精神分裂症,神经疾病如帕森病,神经退行性疾病如阿尔茨海默病,癫痫,偏头痛,高血压,物质滥用和代谢障碍如进食障碍,糖尿病,糖尿病并发症,肥胖症,血脂异常,能量消耗和吸收障碍,体温稳态障碍和功能障碍,睡眠和昼夜节律障碍以及心血管疾病。
  • SUBSTITUTED BENZAMIDE DERIVATIVES
    申请人:F.Hoffmann-La Roche AG
    公开号:EP2516392A1
    公开(公告)日:2012-10-31
  • PYRAZOLE CARBOXAMIDE DERIVATIVES AS TAAR MODULATORS FOR USE IN THE TREATMENT OF SEVERAL DISORDERS, SUCH AS DEPRESSION, DIABETES AND PARKINSON'S DISEASE
    申请人:F.Hoffmann-La Roche AG
    公开号:EP2895477A1
    公开(公告)日:2015-07-22
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