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8-Methyl-3-([1,2,5]thiadiazolo[3',4':4,5]benzimidazo[1,2-c]quinazolin-7-yl)-2H-chromen-2-one | 1266552-38-8

中文名称
——
中文别名
——
英文名称
8-Methyl-3-([1,2,5]thiadiazolo[3',4':4,5]benzimidazo[1,2-c]quinazolin-7-yl)-2H-chromen-2-one
英文别名
8-methyl-3-(7-thia-1,6,8,11,19-pentazapentacyclo[10.8.0.02,10.05,9.013,18]icosa-2(10),3,5,8,11,13,15,17,19-nonaen-20-yl)chromen-2-one
8-Methyl-3-([1,2,5]thiadiazolo[3',4':4,5]benzimidazo[1,2-c]quinazolin-7-yl)-2H-chromen-2-one化学式
CAS
1266552-38-8
化学式
C24H13N5O2S
mdl
——
分子量
435.466
InChiKey
ALLSRMOTZSFDFJ-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):
    5.8
  • 重原子数:
    32
  • 可旋转键数:
    1
  • 环数:
    7.0
  • sp3杂化的碳原子比例:
    0.04
  • 拓扑面积:
    111
  • 氢给体数:
    0
  • 氢受体数:
    7

反应信息

  • 作为产物:
    描述:
    2-(8-methyl-2-oxo-2H-chromen-3-yl)-4H-benzo[d][1,3]oxazin-4-one 、 2,1,3-苯并噻二唑-4,5-二胺 在 cellulose sulfuric acid 作用下, 以 N,N-二甲基甲酰胺 为溶剂, 反应 0.08h, 以95%的产率得到8-Methyl-3-([1,2,5]thiadiazolo[3',4':4,5]benzimidazo[1,2-c]quinazolin-7-yl)-2H-chromen-2-one
    参考文献:
    名称:
    3-[Benzimidazo- and 3-[benzothiadiazoleimidazo-(1,2-c)quinazolin-5-yl]-2H-chromene-2-ones as potent antimicrobial agents
    摘要:
    A series of 3-[benzimidazo(1,2-c) quinazolin-5-yl]-2H-chromene-2-one (6a-6f) and 3-[benzothiadiazoleimidazo( 1,2-c) quinazolin-5-yl]-2H-chromene-2-one derivatives (7a-7f) that incorporate a variety of substituents at the 6-and/or 8-positions of the coumarin moieties have been synthesized utilizing cellulose sulfuric acid as an efficient catalyst under both conventional heating and microwave irradiation procedures. These analogs were evaluated for their antimicrobial activity against Bacillus subtilis, Staphylococcus aureus, Streptococcus pyogenes (Gram-positive bacteria), Escherichia Coli, Klebsiella pneumonia, Salmonella typhimurium (Gram-negative bacteria), and Aspergillus niger, Candida albicans, and Aspergillus flavus (Fungi). Two analogs, 6c (a 6,8-dichloro analog, MIC[SA] = 2.5 mu g/mL; MIC[ST] = 2.5 mu g/mL) and 7d (a 6,8-dibromo analog, MIC[ST] = 2.5 mu g/mL) were identified as potent antibacterial agents, and two analogs, 6b (a 6-bromo analog, MIC[AF] = 10 mu g/mL) and 6d (a 6,8-dibromo analog, MIC[AF] = 15 mu g/mL; MIC[CA] = 15 mu g/mL), were identified as potent antifungal agents. Based on the MIC data, analogs 6b, 6c, 6d, and 7d were identified as the most potent antimicrobial agents in the series. (C) 2010 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2010.10.082
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文献信息

  • 3-[Benzimidazo- and 3-[benzothiadiazoleimidazo-(1,2-c)quinazolin-5-yl]-2H-chromene-2-ones as potent antimicrobial agents
    作者:B. Suresh Kuarm、Y. Thirupathi Reddy、J. Venu Madhav、Peter A. Crooks、B. Rajitha
    DOI:10.1016/j.bmcl.2010.10.082
    日期:2011.1
    A series of 3-[benzimidazo(1,2-c) quinazolin-5-yl]-2H-chromene-2-one (6a-6f) and 3-[benzothiadiazoleimidazo( 1,2-c) quinazolin-5-yl]-2H-chromene-2-one derivatives (7a-7f) that incorporate a variety of substituents at the 6-and/or 8-positions of the coumarin moieties have been synthesized utilizing cellulose sulfuric acid as an efficient catalyst under both conventional heating and microwave irradiation procedures. These analogs were evaluated for their antimicrobial activity against Bacillus subtilis, Staphylococcus aureus, Streptococcus pyogenes (Gram-positive bacteria), Escherichia Coli, Klebsiella pneumonia, Salmonella typhimurium (Gram-negative bacteria), and Aspergillus niger, Candida albicans, and Aspergillus flavus (Fungi). Two analogs, 6c (a 6,8-dichloro analog, MIC[SA] = 2.5 mu g/mL; MIC[ST] = 2.5 mu g/mL) and 7d (a 6,8-dibromo analog, MIC[ST] = 2.5 mu g/mL) were identified as potent antibacterial agents, and two analogs, 6b (a 6-bromo analog, MIC[AF] = 10 mu g/mL) and 6d (a 6,8-dibromo analog, MIC[AF] = 15 mu g/mL; MIC[CA] = 15 mu g/mL), were identified as potent antifungal agents. Based on the MIC data, analogs 6b, 6c, 6d, and 7d were identified as the most potent antimicrobial agents in the series. (C) 2010 Elsevier Ltd. All rights reserved.
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