摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

6,7-Dihydro-9-hydroxy-1-oxo-1H,5H-benzochinolizin-2-carbonsaeure | 42835-58-5

中文名称
——
中文别名
——
英文名称
6,7-Dihydro-9-hydroxy-1-oxo-1H,5H-benzochinolizin-2-carbonsaeure
英文别名
9-hydroxy-1-oxo-6,7-dihydro-1H,5H-pyrido[3,2,1-ij]quinoline-2-carboxylic acid;6,7-dihydro-9-hydroxy-1-oxo-1H,5H-benzo[ij]quinolizine-2-carboxylic acid;9-Hydroxy-1-oxo-6,7-dihydro-1H,5H-pyrido[3,2,1-ij]quinoline-2-carboxylic acid;7-hydroxy-4-oxo-1-azatricyclo[7.3.1.05,13]trideca-2,5,7,9(13)-tetraene-3-carboxylic acid
6,7-Dihydro-9-hydroxy-1-oxo-1H,5H-benzo<ij>chinolizin-2-carbonsaeure化学式
CAS
42835-58-5
化学式
C13H11NO4
mdl
——
分子量
245.235
InChiKey
IPEUOIVHXBNZOQ-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:
    18
  • 可旋转键数:
    1
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.23
  • 拓扑面积:
    77.8
  • 氢给体数:
    2
  • 氢受体数:
    5

反应信息

  • 作为反应物:
    描述:
    6,7-Dihydro-9-hydroxy-1-oxo-1H,5H-benzochinolizin-2-carbonsaeure 在 palladium(II) hydroxide/carbon 盐酸sodium hydroxide氢气potassium carbonate三乙胺 作用下, 以 1,4-二氧六环甲醇 、 DMF (N,N-dimethyl-formamide) 、 二甲基亚砜 为溶剂, 20.0~80.0 ℃ 、344.75 kPa 条件下, 反应 187.0h, 生成 4"-O-{3-[2-(6-carboxy-7-oxo-2,3-dihydro-1H,7H-pyrido[3,2,1-ij]quinolin-9-yloxy)ethylamino]propionyl}-azithromycin tris trifluoroacetate salt
    参考文献:
    名称:
    [EN] MACROLIDES SUBSTITUDED AT THE 4"-POSITION
    [FR] MACROLIDES SUBSTITUES EN POSITION 4''
    摘要:
    本发明涉及在式(I)的4'位置被取代的14-或15-元大环内酯及其药学上可接受的衍生物,以及它们的制备过程和在人体或动物体内治疗或预防全身或局部微生物感染中的用途。
    公开号:
    WO2004101585A1
点击查看最新优质反应信息

文献信息

  • [EN] NOVEL 14 AND 15 MEMBERED-RING COMPOUNDS<br/>[FR] NOUVEAU COMPOSES A CYCLE RAMIFIE EN 14 ET 15.
    申请人:GLAXO GROUP LTD
    公开号:WO2004101586A1
    公开(公告)日:2004-11-25
    The present invention relates to 14- or 15-membered macrolides substituted at the 4' position of formula (I) and pharmaceutically acceptable derivatives thereof, to processes for their preparation and their use in therapy or prophylaxis of systemic or topical microbial infections in a human or animal body.
    本发明涉及在式(I)的14-或15-元大环内在4'位置被取代的大环内酯及其药学上可接受的衍生物,以及它们的制备过程和在人体或动物体内治疗或预防全身或局部微生物感染中的用途。
  • [EN] MACROLIDES SUBSTITUTED AT THE 3-POSITION HAVING ANTIMICROBIAL ACTIVITY<br/>[FR] MACROLIDES SUBSTITUES EN POSITION 3 POSSEDANT UNE ACTIVITE ANTIMICROBIENNE
    申请人:GLAXO GROUP LTD
    公开号:WO2004101584A1
    公开(公告)日:2004-11-25
    The present invention relates to 14- or 15-membered macrolides substituted at the 3-position of formula (I) and pharmaceutically acceptable derivatives thereof, to processes for their preparation and their use in therapy or prophylaxis of systemic or topical microbial infections in a human or animal body.
    本发明涉及在式(I)的3位取代的14-或15元大环内酯及其药学上可接受的衍生物,以及它们的制备过程和在人体或动物体内用于治疗或预防全身或局部微生物感染的用途。
  • Macrolides substituted at the 4"-position
    申请人:Alihodzic Sulejman
    公开号:US20070213283A1
    公开(公告)日:2007-09-13
    The present invention relates to 14- or 15-membered macrolides substituted at the 4″ position of formula (I) and pharmaceutically acceptable derivatives thereof, to processes for their preparation and their use in therapy or prophylaxis of systemic or topical microbial infections in a human or animal body.
    本发明涉及在式(I)的4″位取代的14或15元大环内酯及其药学上可接受的衍生物,以及其制备过程和在人或动物体内治疗或预防全身或局部微生物感染的用途。
  • Novel 14 and 15 membrered ring compounds
    申请人:Alihodzic Sulejman
    公开号:US20070185117A1
    公开(公告)日:2007-08-09
    The present invention relates to 14- or 15-membered macrolides substituted at the 4″ position of formula (I) and pharmaceutically acceptable derivatives thereof, to processes for their preparation and their use in therapy or prophylaxis of systemic or topical microbial infections in a human or animal body.
    本发明涉及在公式(I)的4″位置被取代的14或15元环大环内酯及其药学上可接受的衍生物,以及它们的制备过程和在人或动物体内治疗或预防系统性或局部微生物感染中的用途。
  • 14 and 15 membered ring compounds
    申请人:Glaxo Group Limited
    公开号:US07569550B2
    公开(公告)日:2009-08-04
    The present invention relates to 14- or 15-membered macrolides substituted at the 4″ position of formula (I) and pharmaceutically acceptable derivatives thereof, to processes for their preparation and their use in therapy or prophylaxis of systemic or topical microbial infections in a human or animal body.
    本发明涉及在I式的4″位被取代的14或15元大环内酯及其药学上可接受的衍生物,以及它们的制备方法和在治疗或预防人或动物体内的全身或局部微生物感染中的应用。
查看更多