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7-(3-Amino-5-methyl-1-piperidinyl)-1-cyclopropyl-1,4-dihydro-8-methoxy-4-oxo-3-quinolinecarboxylic acid | 1203651-09-5

中文名称
——
中文别名
——
英文名称
7-(3-Amino-5-methyl-1-piperidinyl)-1-cyclopropyl-1,4-dihydro-8-methoxy-4-oxo-3-quinolinecarboxylic acid
英文别名
7-(3-amino-5-methylpiperidin-1-yl)-1-cyclopropyl-8-methoxy-4-oxoquinoline-3-carboxylic acid
7-(3-Amino-5-methyl-1-piperidinyl)-1-cyclopropyl-1,4-dihydro-8-methoxy-4-oxo-3-quinolinecarboxylic acid化学式
CAS
1203651-09-5
化学式
C20H25N3O4
mdl
——
分子量
371.4
InChiKey
AVPQPGFLVZTJOR-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):
    0.4
  • 重原子数:
    27
  • 可旋转键数:
    4
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.5
  • 拓扑面积:
    96.1
  • 氢给体数:
    2
  • 氢受体数:
    7

文献信息

  • OXIDATIVE COUPLING OF ARYL BORON REAGENTS WITH SP3-CARBON NUCLEOPHILES, AND AMBIENT DECARBOXYLATIVE ARYLATION OF MALONATE HALF-ESTERS VIA OXIDATIVE CATALYSIS
    申请人:The Governors of the University of Alberta
    公开号:US20180186721A1
    公开(公告)日:2018-07-05
    Described herein are methods of oxidative coupling of aryl boron reagents with sp 3 -carbon nucleophiles, and ambient decarboxylative arylation of malonate half-esters via oxidative catalysis.
    本文描述了一种利用氧化偶联芳基硼试剂与sp3-碳亲核试剂进行反应的方法,以及通过氧化催化实现马隆酸半酯的环境脱羧芳基化。
  • Malate salts, and polymorphs of (3S,5S)-7-[3-amino-5-methyl-piperidinyl]-1-cyclopropyl-1,4-dihydro-8-methoxy-4-oxo-3-quinolinecarboxylic acid
    申请人:Redman-Furey Nancy Lee
    公开号:US20070232650A1
    公开(公告)日:2007-10-04
    The present invention is directed to malate salts of (3S,5S)-7-[3-amino-5-methyl-piperidinyl]-1-cyclopropyl-1,4-dihydro-8-methoxy-4-oxo-3-quinolinecarboxylic acid, and its polymorphs. The present invention is also directed to pharmaceutical compositions comprising the described salts and polymorphs.
    本发明涉及(3S,5S)-7-[3-氨基-5-甲基哌啶基]-1-环丙基-1,4-二氢-8-甲氧基-4-氧基-3-喹啉羧酸的苹果酸盐及其多晶形式。本发明还涉及包含所述盐和多晶形式的药物组合物。
  • Hydride reduction process for preparing quinolone intermediates
    申请人:Hayes Michael Patrick
    公开号:US20070232806A1
    公开(公告)日:2007-10-04
    Hydride process for making acyclic diol intermediates from cyclic intermediates, useful in antibacterial quinolone synthesis.
    从环状中间体制备无环二醇中间体的氢化过程,在抗菌喹诺酮合成中很有用。
  • Coupling process for preparing quinolone intermediates
    申请人:Reilly Michael
    公开号:US20070232804A1
    公开(公告)日:2007-10-04
    Process for making 7-cycloamino-1-cyclopropyl-1,4-dihydro-8-methoxy-4-oxo-3-quinolinecarboxylic acids. Borate ester compounds suitable for use in such process.
    制备7-环氨基-1-环丙基-1,4-二氢-8-甲氧基-4-氧代-3-喹啉羧酸的过程。适用于该过程的硼酸酯化合物。
  • Coupling Process For Preparing Quinolone Intermediates
    申请人:Reilly Michael
    公开号:US20090111991A1
    公开(公告)日:2009-04-30
    Process for making 7-cycloamino-1-cyclopropyl-1,4-dihydro-8-methoxy-4-oxo-3-quinolinecarboxylic acids. Borate ester compounds suitable for use in such process.
    制备7-环氨基-1-环丙基-1,4-二氢-8-甲氧基-4-氧代-3-喹啉羧酸的过程。适用于该过程的硼酸酯化合物。
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