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N-(2-(pyridin-2-yl)ethyl)pivalamide | 109902-32-1

中文名称
——
中文别名
——
英文名称
N-(2-(pyridin-2-yl)ethyl)pivalamide
英文别名
2,2-dimethyl-N-(2-pyridin-2-ylethyl)propanamide
N-(2-(pyridin-2-yl)ethyl)pivalamide化学式
CAS
109902-32-1
化学式
C12H18N2O
mdl
——
分子量
206.288
InChiKey
GXAYUAKGAZGTMD-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):
    1.5
  • 重原子数:
    15
  • 可旋转键数:
    4
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.5
  • 拓扑面积:
    42
  • 氢给体数:
    1
  • 氢受体数:
    2

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为产物:
    描述:
    参考文献:
    名称:
    Highly Regioselective Carbonylation of Unactivated C(sp3)–H Bonds by Ruthenium Carbonyl
    摘要:
    The regioselective carbonylation of unactivated C(sp(3))-H bonds of aliphatic amides was achieved using Ru-3(CO)(12) as a catalyst. The presence of a 2-pyridinylmethylamine moiety in the amide is crucial for a successful reaction. The reaction shows a preference for C-H bonds of methyl groups as opposed to methylene C-H bonds and tolerates a variety of functional groups. The stoichiometric reaction of an amide with Ru-3(CO)(12) gave a dinuclear ruthenium complex in which the 2-pyridinylmethylamino moiety was coordinated to the ruthenium center in an N,N manner.
    DOI:
    10.1021/ja2001709
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文献信息

  • HEPATITIS C VIRUS INHIBITORS AND USES THEREOF IN PREPARATION OF DRUGS
    申请人:CHANGZHOU YINSHENG PHARMACEUTICAL CO., LTD.
    公开号:US20170253614A1
    公开(公告)日:2017-09-07
    A series of hepatitis C virus (HCV) inhibitors and compositions and applications thereof in the preparation of drugs for treating chronic HCV infection. Especially, a series of compounds that are used as NS5A inhibitors, and compositions and uses thereof in the preparations of drugs.
    一系列丙型肝炎病毒(HCV)抑制剂及其组合物,以及在制备用于治疗慢性HCV感染的药物时的应用。特别是一系列用作NS5A抑制剂的化合物,以及在药物制剂中的组合物和用途。
  • ARBOVIRUS INHIBITORS AND USES THEREOF
    申请人:Larsen Scott
    公开号:US20120252807A1
    公开(公告)日:2012-10-04
    The present invention relates to chemical compounds, methods for their discovery, and their therapeutic use. In particular, the present invention provides compounds as inhibitors of arboviruses.
    本发明涉及化学化合物、其发现方法以及其治疗用途。具体而言,本发明提供了作为虫媒病毒抑制剂的化合物。
  • DIARYLAMINE-CONTAINING COMPOUNDS AND COMPOSITIONS, AND THEIR USE AS MODULATORS OF C-KIT RECEPTORS
    申请人:Molteni Valentina
    公开号:US20090012094A1
    公开(公告)日:2009-01-08
    Described herein are compounds that include a diarylamine structural feature. Also described herein are methods for making such compounds, methods for using such compounds to modulate the activity of c-kit receptors, and pharmaceutical compositions and medicaments comprising such compounds. Also described herein are methods of using such compounds, pharmaceutical compositions and medicaments to treat and/or prevent and/or inhibit and/or ameliorate the pathology and/or symptomology diseases or conditions associated with the activity of c-kit receptors.
    本文介绍了一种包含二芳胺结构特征的化合物。还介绍了制备这种化合物的方法,使用这种化合物调节c-kit受体活性的方法,以及包含这种化合物的制药组合物和药物。本文还介绍了使用这种化合物、制药组合物和药物治疗和/或预防和/或抑制和/或改善与c-kit受体活性相关的病理学和/或症状学疾病或状况的方法。
  • HYDRAZIDE COMPOUND AND THROMBOPOIETIN RECEPTOR ACTIVATOR
    申请人:Miyaji Katsuaki
    公开号:US20090253751A1
    公开(公告)日:2009-10-08
    Compounds effective for preventing, treatment or improving diseases against which activation of the thrombopoietin receptor is effective are provided. A compound represented by the formula (I) (wherein R 1 , R 2 , R 3 , L 1 , L 2 , X and Y are defined in the description), a tautomer, prodrug or pharmaceutically acceptable salt of the compound or a solvate thereof.
    提供了一种用于预防、治疗或改善激活血小板生成素受体有效对抗的疾病的化合物。该化合物由式(I)所表示(其中R1、R2、R3、L1、L2、X和Y在描述中被定义),该化合物的互变异构体、前药或药物可接受的盐或其溶剂化物。
  • Diarylamine-Containing Compounds and Compositions, and their use as Modulators of C-Kit Receptors
    申请人:Molteni Valentina
    公开号:US20070149538A1
    公开(公告)日:2007-06-28
    Described herein are compounds that include a diarylamine structural feature. Also described herein are methods for making such compounds, methods for using such compounds to modulate the activity of c-kit receptors, and pharmaceutical compositions and medicaments comprising such compounds. Also described herein are methods of using such compounds, pharmaceutical compositions and medicaments to treat and/or prevent and/or inhibit and/or ameliorate the pathology and/or symptomology diseases or conditions associated with the activity of c-kit receptors.
    本文描述了包含二芳胺结构特征的化合物。还描述了制备这种化合物的方法,使用这种化合物调节c-kit受体活性的方法,以及包含这种化合物的药物组合物和药物。本文还描述了使用这种化合物、药物组合物和药物治疗和/或预防和/或抑制和/或改善与c-kit受体活性相关的病理学和/或症状学疾病或状况的方法。
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