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2,6-dimethylheptan-4-amine hydrochloride | 130996-65-5

中文名称
——
中文别名
——
英文名称
2,6-dimethylheptan-4-amine hydrochloride
英文别名
1-isobutyl-3-methyl-butylamin; hydrochloride;2,6-Dimethyl-4-aminoheptane Hydrochloride;2,6-dimethylheptan-4-amine;hydrochloride
2,6-dimethylheptan-4-amine hydrochloride化学式
CAS
130996-65-5
化学式
C9H21N*ClH
mdl
MFCD17480397
分子量
179.733
InChiKey
MIIOSNBDDPBLBR-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):
    2.66
  • 重原子数:
    11
  • 可旋转键数:
    4
  • 环数:
    0.0
  • 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:
    1

反应信息

  • 作为反应物:
    描述:
    2,6-dimethylheptan-4-amine hydrochloride(3S,5R)-1-(tert-butoxycarbonyl)-5-(methoxycarbonyl)piperidine-3-carboxylic acid 在 O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate 、 N,N-二异丙基乙胺 作用下, 以 N,N-二甲基甲酰胺 为溶剂, 反应 18.0h, 以75%的产率得到3-methyl (3R,5S)-5-[(1-isobutyl-3-methylbutyl)carbamoyl]piperidine-1,3-dicarboxylate
    参考文献:
    名称:
    Synthesis and optimization of novel (3S,5R)-5-(2,2-dimethyl-5-oxo-4-phenylpiperazin-1-yl)piperidine-3-carboxamides as orally active renin inhibitors
    摘要:
    We report synthesis and optimization of a series of (3S,5R)-5-(2,2-dimethyl-5-oxo-4-phenylpiperazin-1-yl)piperidine-3-carboxamides as renin inhibitors. Chemical modification of P-1', P-2' and P-3 portions led to a promising 3,5-disubstituted piperidine 32o showing high renin inhibitory activity and favorable oral exposure in both rats and cynomolgus monkeys with acceptable CYP and hERG current inhibition. Compound 32o exhibited a significant blood pressure lowering effect by oral administration in two hypertensive animal models, double transgenic rats and furosemide pretreated cynomolgus monkeys. (C) 2013 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmc.2013.06.057
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文献信息

  • Organic Compounds
    申请人:Ehara Takeru
    公开号:US20090192148A1
    公开(公告)日:2009-07-30
    The invention relates to 3,5-substituted piperidine compounds, these compounds for use in the diagnostic and therapeutic treatment of a warm-blooded animal, especially for the treatment of a disease (=disorder) that depends on activity of renin; the use of a compound of that class for the preparation of a pharmaceutical formulation for the treatment of a disease that depends on activity of renin; the use of a compound of that class in the treatment of a disease that depends on activity of renin; pharmaceutical formulations comprising a 3,5-substituted piperidine compound, and/or a method of treatment comprising administering a 3,5-substituted piperidine compound, a method for the manufacture of a 3,5-substituted piperidine compound, and novel intermediates and partial steps for its synthesis. The compounds have the formula I′ wherein R1, R2, T, R3 and R4 areas defined in the specification.
    本发明涉及3,5-取代哌啶化合物,这些化合物用于诊断和治疗温血动物,特别是用于治疗依赖肾素活性的疾病(=失调);该类化合物用于制备治疗依赖肾素活性疾病的制剂;该类化合物用于治疗依赖肾素活性的疾病;包括3,5-取代哌啶化合物的制药配方和/或包括给予3,5-取代哌啶化合物的治疗方法,以及制造3,5-取代哌啶化合物的新型中间体和部分合成步骤。该化合物的式子为I',其中R1、R2、T、R3和R4在规范中有定义。
  • Gastrin releasing peptide antagonists
    申请人:Merck & Co., Inc.
    公开号:EP0371543A2
    公开(公告)日:1990-06-06
    Small cell lung carcinoma (SCLC) cells contain gastrin releasing peptide (GRP) receptors. The response of the cells to GRP is rapid growth. We have found a group of peptide derivatives that act as GRP antagonists by blocking the binding of GRP to its receptor thereby inhibiting the growth of cells that are sensitive to the growth promoting activity of GRP.
    小细胞肺癌(SCLC)细胞含有胃泌素释放肽(GRP)受体。细胞对 GRP 的反应是快速生长。我们发现一组肽衍生物可作为 GRP 拮抗剂,通过阻断 GRP 与其受体的结合,从而抑制对 GRP 促进生长活性敏感的细胞的生长。
  • 3 , 5-substitued piperidine compounds as renin inhibitors
    申请人:Novartis AG
    公开号:EP2420491A1
    公开(公告)日:2012-02-22
    The invention relates to 3,5-substituted piperidine compounds, these compounds for use in the diagnostic and therapeutic treatment of a warm-blooded animal, especially for the treatment of a disease (= disorder) that depends on activity of renin; the use of a compound of that class for the preparation of a pharmaceutical formulation for the treatment of a disease that depends on activity of renin; the use of a compound of that class in the treatment of a disease that depends on activity of renin; pharmaceutical formulations comprising a 3,5-substituted piperidine compound, and/or a method of treatment comprising administering a 3,5-substituted piperidine compound, a method for the manufacture of a 3, 5-substituted piperidine compound, and novel intermediates and partial steps for its synthesis. The compounds (which can also be present as salts) have the formula I' wherein R1, R2, T, R3, R4, R7 and R8 are as defined in the specification and R6 is OH.
    本发明涉及3,5-取代的哌啶化合物,这些化合物用于温血动物的诊断和治疗,特别是用于治疗依赖于肾素活性的疾病(=紊乱);使用该类化合物制备药物制剂,用于治疗依赖于肾素活性的疾病;该类化合物在治疗依赖于肾素活性的疾病中的用途;包含 3,5-取代的哌啶化合物的药物制剂,和/或包括施用 3,5-取代的哌啶化合物的治疗方法,3,5-取代的哌啶化合物的制造方法,及其合成的新型中间体和部分步骤。 这些化合物(也可以以盐的形式存在)具有式 I' 其中 R1、R2、T、R3、R4、R7 和 R8 如说明书中所定义,R6 为 OH。
  • 3 , 5-SUBSTITUED PIPERIDINE COMPOUNDS AS RENIN INHIBITORS
    申请人:Novartis AG
    公开号:EP1968940A1
    公开(公告)日:2008-09-17
  • US4943561A
    申请人:——
    公开号:US4943561A
    公开(公告)日:1990-07-24
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