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

4-bromomethyl-7-methyl-coumarin-6-sulfonyl chloride | 1220529-06-5

中文名称
——
中文别名
——
英文名称
4-bromomethyl-7-methyl-coumarin-6-sulfonyl chloride
英文别名
4-(Bromomethyl)-7-methyl-2-oxochromene-6-sulfonyl chloride
4-bromomethyl-7-methyl-coumarin-6-sulfonyl chloride化学式
CAS
1220529-06-5
化学式
C11H8BrClO4S
mdl
——
分子量
351.605
InChiKey
DRVAFGCZHVHINC-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):
    2.4
  • 重原子数:
    18
  • 可旋转键数:
    2
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.18
  • 拓扑面积:
    68.8
  • 氢给体数:
    0
  • 氢受体数:
    4

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
  • 下游产品
    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:
    4-bromomethyl-7-methyl-coumarin-6-sulfonyl chloride 在 sodium azide 作用下, 以 丙酮 为溶剂, 反应 10.0h, 以65%的产率得到4-azidomethyl-7-methyl-coumarin-6-sulfonyl chloride
    参考文献:
    名称:
    Synthesis and antimicrobial studies on novel sulfonamides containing 4-azidomethyl coumarin
    摘要:
    A series of new and novel coumarin-6-sulfonamides with a free C4-azidomethyl group have been synthesized as antimicrobials in three steps starting from 7-methyl-4-bromomethylcoumarin 1. The reaction of I with chlorosulfonic acid was found to yield the corresponding 6-sulfonylchloride 2, which when treated with sodium azide led to intermediate 3. The title sulfonamides 5a-y were obtained from the reaction of 3 with various aromatic amines 4 in refluxing benzene. The chemical structures of the compounds were elucidated by IR, NMR and LC-MS spectral data. All the synthesized compounds have been screened for their in vitro anti-bacterial and anti-fungal activities. Some of the Compounds have been found to be active against both bacterial species at a concentration of 1 mu g/mL. (C) 2009 Elsevier Masson SAS. All rights reserved.
    DOI:
    10.1016/j.ejmech.2009.12.022
  • 作为产物:
    描述:
    4-bromomethyl-7-methyl-coumarin氯磺酸 作用下, 以55%的产率得到4-bromomethyl-7-methyl-coumarin-6-sulfonyl chloride
    参考文献:
    名称:
    Synthesis and antimicrobial studies on novel sulfonamides containing 4-azidomethyl coumarin
    摘要:
    A series of new and novel coumarin-6-sulfonamides with a free C4-azidomethyl group have been synthesized as antimicrobials in three steps starting from 7-methyl-4-bromomethylcoumarin 1. The reaction of I with chlorosulfonic acid was found to yield the corresponding 6-sulfonylchloride 2, which when treated with sodium azide led to intermediate 3. The title sulfonamides 5a-y were obtained from the reaction of 3 with various aromatic amines 4 in refluxing benzene. The chemical structures of the compounds were elucidated by IR, NMR and LC-MS spectral data. All the synthesized compounds have been screened for their in vitro anti-bacterial and anti-fungal activities. Some of the Compounds have been found to be active against both bacterial species at a concentration of 1 mu g/mL. (C) 2009 Elsevier Masson SAS. All rights reserved.
    DOI:
    10.1016/j.ejmech.2009.12.022
点击查看最新优质反应信息

文献信息

  • Synthesis and antimicrobial studies on novel sulfonamides containing 4-azidomethyl coumarin
    作者:Mahantesha Basanagouda、K. Shivashankar、Manohar V. Kulkarni、Vijaykumar P. Rasal、Harishchandra Patel、Sumit S. Mutha、Ashwini A. Mohite
    DOI:10.1016/j.ejmech.2009.12.022
    日期:2010.3
    A series of new and novel coumarin-6-sulfonamides with a free C4-azidomethyl group have been synthesized as antimicrobials in three steps starting from 7-methyl-4-bromomethylcoumarin 1. The reaction of I with chlorosulfonic acid was found to yield the corresponding 6-sulfonylchloride 2, which when treated with sodium azide led to intermediate 3. The title sulfonamides 5a-y were obtained from the reaction of 3 with various aromatic amines 4 in refluxing benzene. The chemical structures of the compounds were elucidated by IR, NMR and LC-MS spectral data. All the synthesized compounds have been screened for their in vitro anti-bacterial and anti-fungal activities. Some of the Compounds have been found to be active against both bacterial species at a concentration of 1 mu g/mL. (C) 2009 Elsevier Masson SAS. All rights reserved.
查看更多