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1-(2,2,2-trifluoroethyl)cyclopropan-1-amine hydrochloride | 1461714-70-4

中文名称
——
中文别名
——
英文名称
1-(2,2,2-trifluoroethyl)cyclopropan-1-amine hydrochloride
英文别名
1-(2,2,2-trifluoroethyl)cyclopropan-1-amine;hydrochloride
1-(2,2,2-trifluoroethyl)cyclopropan-1-amine hydrochloride化学式
CAS
1461714-70-4
化学式
C5H8F3N*ClH
mdl
MFCD25970470
分子量
175.581
InChiKey
ZRQIABHOHKJUBM-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

计算性质

  • 辛醇/水分配系数(LogP):
    0.63
  • 重原子数:
    10
  • 可旋转键数:
    1
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    26
  • 氢给体数:
    2
  • 氢受体数:
    4

反应信息

  • 作为反应物:
    描述:
    1-(2,2,2-trifluoroethyl)cyclopropan-1-amine hydrochloride 、 4-chloro-5-(6-chloro-4-methoxypyridin-3-yl)-1-ethyl-N-(((1r,4r)-4-(methylsulfonyl)cyclohexyl)methyl)-1H-pyrazole-3-carboxamide 在 [(2-di-cyclohexylphosphino-3,6-dimethoxy-2’,4’,6’-triisopropyl-1,1‘-biphenyl)-2-(2‘-amino-1,1’-biphenyl)]palladium(II) methanesulfonate 、 sodium t-butanolate 作用下, 以 1,4-二氧六环 为溶剂, 生成 4-chloro-1-ethyl-5-(4-methoxy-6-((1-(2,2,2-trifluoroethyl)cyclopropyl)amino)pyridin-3-yl)-N-(((1r,4r)-4-(methylsulfonyl)cyclohexyl)methyl)-1H-pyrazole-3-carboxamide
    参考文献:
    名称:
    6-AMINOPYRIDIN-3-YL PYRAZOLES AS MODULATORS OF RORgT
    摘要:
    本发明涵盖了Formula I中的化合物,其中:R1、Q、R3、R4、R5、R6、A1和A2在规范中有定义。该发明还涵盖了一种治疗或改善ROR-γ-t介导的综合征、疾病或疾病的方法,包括综合征、疾病或疾病选自风湿性关节炎、银屑病性关节炎和银屑病的群体。该发明还涵盖了通过给哺乳动物施用至少一种Formula I化合物的治疗有效量来调节RORγt活性的方法。
    公开号:
    US20190382373A1
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文献信息

  • POSITIVE ALLOSTERIC MODULATORS OF MUSCARINIC M2 RECEPTOR
    申请人:Bayer Pharma Aktiengesellschaft
    公开号:US20180297994A1
    公开(公告)日:2018-10-18
    The present application relates to positive allosteric modulators of the muscarinic M2 receptor, especially to novel 7-substituted 1-arylnaphthyridine-3-carboxamides, to processes for preparation thereof, to the use thereof, alone or in combinations, for treatment and/or prevention of diseases, and to the use thereof for production of medicaments for treatment and/or prevention of diseases, in particular for treatment and/or prevention of cardiovascular disorders and/or renal disorders.
    本申请涉及肌动蛋白M2受体的阳性变构调节剂,特别是新型的7-取代的1-芳基啶-3-羧酰胺,以及其制备方法,单独或组合使用于治疗和/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/或预防心血管疾病和/或肾脏疾病。
  • Positive allosteric modulators of muscarinic M2 receptor
    申请人:Bayer Pharma Aktiengesellschaft
    公开号:US10435403B2
    公开(公告)日:2019-10-08
    The present application relates to positive allosteric modulators of the muscarinic M2 receptor, especially to novel 7-substituted 1-arylnaphthyridine-3-carboxamides, to processes for preparation thereof, to the use thereof, alone or in combinations, for treatment and/or prevention of diseases, and to the use thereof for production of medicaments for treatment and/or prevention of diseases, in particular for treatment and/or prevention of cardiovascular disorders and/or renal disorders.
    本申请涉及毒蕈碱 M2 受体的正性异位调节剂,特别是新型 7-取代 1-芳基啶-3-羧酰胺,涉及其制备工艺,涉及其单独或组合用于治疗和/或预防疾病,以及涉及其用于生产治疗和/或预防疾病的药物,特别是用于治疗和/或预防心血管疾病和/或肾脏疾病。
  • 6-aminopyridin-3-yl pyrazoles as modulators of RORgT
    申请人:Janssen Pharmaceutica NV
    公开号:US10975057B2
    公开(公告)日:2021-04-13
    The present invention comprises compounds of Formula I. wherein: R1, Q, R3, R4, R5, R6, A1, and A2 are defined in the specification. The invention also comprises a method of treating or ameliorating a ROR-γ-t mediated syndrome, disorder or disease, including wherein the syndrome, disorder or disease is selected from the group consisting of rheumatoid arthritis, psoriatic arthritis, and psoriasis. The invention also comprises a method of modulating RORγt activity in a mammal by administration of a therapeutically effective amount of at least one compound of Formula I.
    本发明包括式 I 的化合物。 其中 R1、Q、R3、R4、R5、R6、A1 和 A2 的定义见说明书。 本发明还包括一种治疗或改善 ROR-γ-t 介导的综合征、紊乱或疾病的方法,其中综合征、紊乱或疾病选自由类风湿性关节炎、屑病关节炎和屑病组成的组。本发明还包括一种通过施用治疗有效量的至少一种式 I 化合物来调节哺乳动物体内 RORγt 活性的方法。
  • NOVEL HETEROARYL-UREA COMPOUNDS AS KV7.2 INHIBITORS
    申请人:[en]ICAGEN, LLC
    公开号:WO2023091554A1
    公开(公告)日:2023-05-25
    The invention provides new heteroaromatic compounds having the general formula (I'), or a solvate or a pharmaceutically acceptable salt thereof, wherein R1, R2, R3, R4, R5, R6, Y1, Y2, Y3, and n are as defined herein, compositions including the compounds, processes of manufacturing the compounds and methods of using the compounds.
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