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-(but-3-enyl)-9-fluoro-2-(4-methoxy-benzyl)-3,4-dihydro-2H-benzo[b][1,4,5]oxathiazepine 1,1-dioxide | 1216844-58-4

中文名称
——
中文别名
——
英文名称
4-(but-3-enyl)-9-fluoro-2-(4-methoxy-benzyl)-3,4-dihydro-2H-benzo[b][1,4,5]oxathiazepine 1,1-dioxide
英文别名
4-But-3-enyl-9-fluoro-2-[(4-methoxyphenyl)methyl]-3,4-dihydro-5,1lambda6,2-benzoxathiazepine 1,1-dioxide;4-but-3-enyl-9-fluoro-2-[(4-methoxyphenyl)methyl]-3,4-dihydro-5,1λ6,2-benzoxathiazepine 1,1-dioxide
4-(but-3-enyl)-9-fluoro-2-(4-methoxy-benzyl)-3,4-dihydro-2H-benzo[b][1,4,5]oxathiazepine 1,1-dioxide化学式
CAS
1216844-58-4
化学式
C20H22FNO4S
mdl
——
分子量
391.463
InChiKey
UCHPVGOACKENTC-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):
    3.9
  • 重原子数:
    27
  • 可旋转键数:
    6
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.3
  • 拓扑面积:
    64.2
  • 氢给体数:
    0
  • 氢受体数:
    6

上下游信息

  • 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:
    3,4,5-三甲氧基苄胺4-(but-3-enyl)-9-fluoro-2-(4-methoxy-benzyl)-3,4-dihydro-2H-benzo[b][1,4,5]oxathiazepine 1,1-dioxidecaesium carbonate 作用下, 以 二甲基亚砜 为溶剂, 反应 0.5h, 以31%的产率得到4-but-3-enyl-2-[(4-methoxyphenyl)methyl]-1,1-dioxo-N-[(3,4,5-trimethoxyphenyl)methyl]-3,4-dihydro-5,1lambda6,2-benzoxathiazepin-9-amine
    参考文献:
    名称:
    SNAr-Based, Facile Synthesis of a Library of Benzothiaoxazepine-1,1′-dioxides
    摘要:
    The construction of a library of benzothiaoxazepine-1,1'-dioxides utilizing a one-pot, SNAr diversification ODCT50 scavenging protocol is reported. This protocol combines microwave irradiation to facilitate the reaction, in conjunction with a soluble ROMP-derived scavenger (ODCT) to afford the desired products in good overall purity. Utilizing this protocol, a 78-member library was successfully synthesized and submitted for biological evaluation.
    DOI:
    10.1021/cc1001023
  • 作为产物:
    描述:
    1,2-环氧基-5-己烯2,6-difluoro-N-[(4-methoxyphenyl)methyl]benzenesulfonamide苄基三乙基氯化铵caesium carbonate 作用下, 以 四氢呋喃1,4-二氧六环N,N-二甲基甲酰胺 为溶剂, 反应 0.33h, 以69%的产率得到4-(but-3-enyl)-9-fluoro-2-(4-methoxy-benzyl)-3,4-dihydro-2H-benzo[b][1,4,5]oxathiazepine 1,1-dioxide
    参考文献:
    名称:
    SNAr-Based, Facile Synthesis of a Library of Benzothiaoxazepine-1,1′-dioxides
    摘要:
    The construction of a library of benzothiaoxazepine-1,1'-dioxides utilizing a one-pot, SNAr diversification ODCT50 scavenging protocol is reported. This protocol combines microwave irradiation to facilitate the reaction, in conjunction with a soluble ROMP-derived scavenger (ODCT) to afford the desired products in good overall purity. Utilizing this protocol, a 78-member library was successfully synthesized and submitted for biological evaluation.
    DOI:
    10.1021/cc1001023
点击查看最新优质反应信息

文献信息

  • 10.1021/0l100035e
    作者:Rolfe, Alan、Samarakoon, Thiwanka B.、Hanson, Paul R.
    DOI:10.1021/0l100035e
    日期:——
  • S<sub>N</sub>Ar-Based, Facile Synthesis of a Library of Benzothiaoxazepine-1,1′-dioxides
    作者:Alan Rolfe、Thiwanka B. Samarakoon、Sarra V. Klimberg、Marek Brzozowski、Benjamin Neuenswander、Gerald H. Lushington、Paul R. Hanson
    DOI:10.1021/cc1001023
    日期:2010.11.8
    The construction of a library of benzothiaoxazepine-1,1'-dioxides utilizing a one-pot, SNAr diversification ODCT50 scavenging protocol is reported. This protocol combines microwave irradiation to facilitate the reaction, in conjunction with a soluble ROMP-derived scavenger (ODCT) to afford the desired products in good overall purity. Utilizing this protocol, a 78-member library was successfully synthesized and submitted for biological evaluation.
查看更多