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(S)-N-[3-(3-benzothiazol-2-yl-1,4,5,6-tetrahydro-1,2-diaza-benzo[e]azulen-8-yl)-2-oxo-oxazolidin-5-ylmethyl]-acetamide

中文名称
——
中文别名
——
英文名称
(S)-N-[3-(3-benzothiazol-2-yl-1,4,5,6-tetrahydro-1,2-diaza-benzo[e]azulen-8-yl)-2-oxo-oxazolidin-5-ylmethyl]-acetamide
英文别名
N-[[(5S)-3-[5-(1,3-benzothiazol-2-yl)-3,4-diazatricyclo[8.4.0.02,6]tetradeca-1(10),2,5,11,13-pentaen-12-yl]-2-oxo-1,3-oxazolidin-5-yl]methyl]acetamide
(S)-N-[3-(3-benzothiazol-2-yl-1,4,5,6-tetrahydro-1,2-diaza-benzo[e]azulen-8-yl)-2-oxo-oxazolidin-5-ylmethyl]-acetamide化学式
CAS
——
化学式
C25H23N5O3S
mdl
——
分子量
473.555
InChiKey
BCBGJUUDTHQYMA-KRWDZBQOSA-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):
    3.8
  • 重原子数:
    34
  • 可旋转键数:
    4
  • 环数:
    6.0
  • sp3杂化的碳原子比例:
    0.28
  • 拓扑面积:
    128
  • 氢给体数:
    2
  • 氢受体数:
    6

反应信息

  • 作为产物:
    描述:
    n-{3-[6(r,s)-(Benzothiazole-2-carbonyl)-5-oxo-6,7,8,9-tetrahydro-5h-benzocyclohepten-2-yl]-2-oxo-oxazolidin-5(s)-ylmethyl}-acetamide 在 一水合肼 作用下, 以 乙醇 为溶剂, 生成 (S)-N-[3-(3-benzothiazol-2-yl-1,4,5,6-tetrahydro-1,2-diaza-benzo[e]azulen-8-yl)-2-oxo-oxazolidin-5-ylmethyl]-acetamide
    参考文献:
    名称:
    Synthesis and SAR of novel conformationally-restricted oxazolidinones possessing Gram-positive and fastidious Gram-negative antibacterial activity. Part 1: Substituted pyrazoles
    摘要:
    A novel series of conformationally-restricted oxazolidinones was synthesized which possess a fused pyrazole ring substituted with various alkyl, aryl and heteroaryl substituents. A number of analogs exhibited potent activity against both Gram-positive and fastidious Gram-negative organisms.(c) 2007 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2007.05.056
  • 作为试剂:
    描述:
    n-{3-[6(r,s)-(Benzothiazole-2-carbonyl)-5-oxo-6,7,8,9-tetrahydro-5h-benzocyclohepten-2-yl]-2-oxo-oxazolidin-5(s)-ylmethyl}-acetamide 、 一水合肼(S)-N-[3-(3-benzothiazol-2-yl-1,4,5,6-tetrahydro-1,2-diaza-benzo[e]azulen-8-yl)-2-oxo-oxazolidin-5-ylmethyl]-acetamidemethanol-dichloromethane甲醇 作用下, 以 乙醇 为溶剂, 反应 1.67h, 以10 minutes, then 7-9% MeOH over 30 minutes) to afford the title compound的产率得到(S)-N-[3-(3-benzothiazol-2-yl-1,4,5,6-tetrahydro-1,2-diaza-benzo[e]azulen-8-yl)-2-oxo-oxazolidin-5-ylmethyl]-acetamide
    参考文献:
    名称:
    Antibacterial agents
    摘要:
    本文披露了I式化合物及其制备方法。此外,还披露了制备具有生物活性的I式化合物的方法,以及包含I式化合物的药学上可接受的组合物的方法。本文所披露的I式化合物可以用于多种应用,包括用作抗菌剂。
    公开号:
    US20050288273A1
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文献信息

  • ANTIBACTERIAL AGENTS
    申请人:Warner-Lambert Company LLC
    公开号:EP1594865A2
    公开(公告)日:2005-11-16
  • [EN] ANTIBACTERIAL AGENTS<br/>[FR] AGENTS ANTIBACTERIENS
    申请人:WARNER LAMBERT CO
    公开号:WO2004069832A2
    公开(公告)日:2004-08-19
    Compounds of formula (I) and methods for their preparation are disclosed. Further disclosed are methods of making biologically active compounds of formula I as well as pharmaceutically acceptable compositions comprising compounds of formula (I). Compounds of formula I as disclosed herein can be used in a variety of applications including use as antibacterial agents. Formula (I): wherein P is Formula (II), Formula (III), Formula (IV) or Formula (V).
  • Synthesis and SAR of novel conformationally-restricted oxazolidinones possessing Gram-positive and fastidious Gram-negative antibacterial activity. Part 1: Substituted pyrazoles
    作者:Frederick E. Boyer、J.V.N. Vara Prasad、Allison L. Choy、Louis Chupak、Michael R. Dermyer、Qizhu Ding、Michael D. Huband、Wenhua Jiao、Takushi Kaneko、Vladimir Khlebnikov、Ji-Young Kim、Manjinder S. Lall、Samarendra N. Maiti、Karina Romero、Xiujuan Wu
    DOI:10.1016/j.bmcl.2007.05.056
    日期:2007.8
    A novel series of conformationally-restricted oxazolidinones was synthesized which possess a fused pyrazole ring substituted with various alkyl, aryl and heteroaryl substituents. A number of analogs exhibited potent activity against both Gram-positive and fastidious Gram-negative organisms.(c) 2007 Elsevier Ltd. All rights reserved.
  • Antibacterial agents
    申请人:Boyer Earl Frederick
    公开号:US20050288273A1
    公开(公告)日:2005-12-29
    Compounds of formula I and methods for their preparation are disclosed. Further disclosed are methods of making biologically active compounds of formula I as well as pharmaceutically acceptable compositions comprising compounds of formula I. Compounds of formula I as disclosed herein can be used in a variety of applications including use as antibacterial agents.
    本文披露了I式化合物及其制备方法。此外,还披露了制备具有生物活性的I式化合物的方法,以及包含I式化合物的药学上可接受的组合物的方法。本文所披露的I式化合物可以用于多种应用,包括用作抗菌剂。
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