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4-dimethylamino-3,3-dimethylpiperidine | 544443-33-6

中文名称
——
中文别名
——
英文名称
4-dimethylamino-3,3-dimethylpiperidine
英文别名
N,N,3,3-tetramethylpiperidin-4-amine
4-dimethylamino-3,3-dimethylpiperidine化学式
CAS
544443-33-6
化学式
C9H20N2
mdl
——
分子量
156.271
InChiKey
LTVSDBIRNKOKKA-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):
    1.2
  • 重原子数:
    11
  • 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:
    15.3
  • 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

  • 作为反应物:
    描述:
    (1-cyclopropyl-6,7-difluoro-1,4-dihydro-8-methoxy-4-(oxo-κO)-3-quinoline-carboxylato-κO3)difluoro-Boron 、 4-dimethylamino-3,3-dimethylpiperidine三乙胺 作用下, 以 乙腈乙醇 为溶剂, 反应 22.0h, 以35%的产率得到1-Cyclopropyl-6-fluoro-1,4-dihydro-8-methoxy-7-(4-dimethylamino-3,3-dimethyl-1-piperidinyl)-4-oxo-quinoline-3-carboxylic acid
    参考文献:
    名称:
    WCK 1152, WCK 1153: Discovery and structure activity relationship for the treatment of resistant pneumococcal and staphylococcal respiratory infections
    摘要:
    DOI:
    10.1016/j.bmcl.2022.128665
  • 作为产物:
    描述:
    1-benzyl-4-dimethylamino-3,3-dimethylpiperidine氢氧化钯 甲醇 作用下, 以 甲醇氢气 为溶剂, 25.0 ℃ 、13.51 MPa 条件下, 反应 48.0h, 以to afford 4-dimethylamino-3,3-dimethylpiperidine的产率得到4-dimethylamino-3,3-dimethylpiperidine
    参考文献:
    名称:
    Generation triple-targeting, chiral, broad-spectrum antimicrobial 7-substituted piperidino-quinolone carboxylic acid derivatives, their preparation, compositions and use as medicaments
    摘要:
    本发明涉及新一代三重靶向手性广谱抗微生物7-取代哌啶酮羧酸衍生物,以及它们的光学异构体、对映异构体或对映体,以及其制备方法、组成物和用途,还包括药学上可接受的盐、水合物、前药、多晶形和伪多晶形。
    公开号:
    US07626032B2
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文献信息

  • Azaquinazoline Inhibitors Of Atypical Protein Kinase C
    申请人:Ignyta, Inc.
    公开号:US20150274720A1
    公开(公告)日:2015-10-01
    The present application provides a compound of formula (I) and/or a salt thereof, wherein R 1 , G, and X are as defined herein. A compound of formula (I) and/or its salts have aPKC inhibitory activity, and may be used to treat proliferative disorders. Compositions comprising a compound of Formula (I) and/or a salt thereof are also provided.
    本申请提供了一种具有化学式(I)的化合物和/或其盐,其中R1、G和X如本文所定义。化合物的化学式(I)和/或其盐具有aPKC抑制活性,并可用于治疗增生性疾病。还提供了包含化学式(I)的化合物和/或其盐的组合物。
  • [EN] FLUOROMETHYL-SUBSTITUTED PYRROLE CARBOXAMIDES III<br/>[FR] PYRROLE CARBOXAMIDES III SUBSTITUÉS PAR DU FLUOROMÉTHYLE
    申请人:GRUENENTHAL GMBH
    公开号:WO2015090603A1
    公开(公告)日:2015-06-25
    The invention relates to pyrrole carboxamides bearing a fluoromethyl- moiety as voltage gated calcium channel blockers, to pharmaceutical compositions containing these compounds and also to these compounds for use in the treatment and/or prophylaxis of pain and further diseases and/or disorders.
    该发明涉及带有氟甲基基团的吡咯羧酰胺作为电压门控钙通道阻滞剂,以及含有这些化合物的药物组合物,还涉及这些化合物用于治疗和/或预防疼痛以及其他疾病和/或紊乱。
  • Generation triple-targeting, chiral, broad-spectrum antimicrobial 7-substituted piperidino-quinolone carboxylic acid derivatives, their preparation,compositions and use as medicaments
    申请人:WOCKHARDT LIMITED
    公开号:US20030216568A1
    公开(公告)日:2003-11-20
    This invention relates to new generation triple-targeting, chiral, broad-spectrum antimicrobial 7-substituted piperidino-quinolone carboxylic acid derivatives, to their optical isomers, diastereomers or enantiomers, as well as pharmaceutically acceptable salts, hydrates, prodrugs, polymorphs and pseudopolymorphs thereof, to their preparation, to their compositions and to their use.
    本发明涉及新一代三重靶向手性广谱抗菌7-取代哌啶酮羧酸衍生物,以及它们的光学异构体、对映异构体或对映体,以及其药学上可接受的盐、水合物、前药、多晶形和假多晶形,以及它们的制备、组成和用途。
  • Generation triple-targeting, chiral, broad-spectrum antimicrobial 7-substituted piperidino-Quinolone carboxylic acid derivatives, their preparation, compositions and use as medicaments
    申请人:WOCKHARDT LIMITED
    公开号:US20030096812A1
    公开(公告)日:2003-05-22
    This invention relates to new generation triple-targeting, chiral, broad-spectrum antimicrobial 7-substituted piperidino-quinolone carboxylic acid derivatives, to their optical isomers, diastereomers or enantiomers, as well as pharmaceutically acceptable salts, hydrates, prodrugs, polymorphs and pseudopolymorphs thereof, to their preparation, to their compositions and to their use.
    本发明涉及新一代三重靶向手性广谱抗微生物7-取代哌啶酮羧酸衍生物,其光学异构体,对映异构体或对映体,以及其药学上可接受的盐,水合物,前药,多晶形和假多晶形,以及其制备,组成和使用。
  • New generation triple-targeting, chiral, broad-spectrum antimicrobial 7-substituted piperidino-quinolone carboxylic acid derivatives, their preparation, compositions and use as medicaments
    申请人:De Souza Noel John
    公开号:US20080214608A1
    公开(公告)日:2008-09-04
    This invention relates to new generation triple-targeting, chiral, broad-spectrum antimicrobial 7-substituted piperidino-quinolone carboxylic acid derivatives, to their optical isomers, diastereomers or enantiomers, as well as pharmaceutically acceptable salts, hydrates, prodrugs, polymorphs and pseudopolymorphs thereof, to their preparation, to their compositions and to their use.
    本发明涉及新一代三重靶向手性广谱抗微生物7-取代哌啶酮羧酸衍生物,以及它们的光学异构体、对映异构体或对映体,以及药学上可接受的盐、水合物、前药、多晶形和伪多晶形,以及它们的制备、组成和使用。
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