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3-chloro-6-(3-fluorobenzyl)-6,7-dihydrodibenzo[b,g][1,4,5]oxathiazocine 5,5-dioxide | 1225039-97-3

中文名称
——
中文别名
——
英文名称
3-chloro-6-(3-fluorobenzyl)-6,7-dihydrodibenzo[b,g][1,4,5]oxathiazocine 5,5-dioxide
英文别名
8-chloro-11-[(3-fluorophenyl)methyl]-12H-benzo[d][6,1,2]benzoxathiazocine 10,10-dioxide
3-chloro-6-(3-fluorobenzyl)-6,7-dihydrodibenzo[b,g][1,4,5]oxathiazocine 5,5-dioxide化学式
CAS
1225039-97-3
化学式
C20H15ClFNO3S
mdl
——
分子量
403.861
InChiKey
RYGSVXLJZDMLEI-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):
    4.4
  • 重原子数:
    27
  • 可旋转键数:
    2
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.1
  • 拓扑面积:
    55
  • 氢给体数:
    0
  • 氢受体数:
    5

反应信息

  • 作为产物:
    描述:
    5-chloro-2-fluoro-N-(3-fluorobenzyl)benzenesulfonamide 、 Acetic acid 2-(tert-butyl-dimethyl-silanyloxy)-benzyl ester 在 四丁基氟化铵 作用下, 以 四氢呋喃 为溶剂, 反应 0.5h, 以87%的产率得到3-chloro-6-(3-fluorobenzyl)-6,7-dihydrodibenzo[b,g][1,4,5]oxathiazocine 5,5-dioxide
    参考文献:
    名称:
    A Formal [4 + 4] Complementary Ambiphile Pairing Reaction: A New Cyclization Pathway for ortho-Quinone Methides
    摘要:
    A formal, one-pot [4 + 4] cyclization pathway for the generation of eight-membered sultams via in situ generation of an ortho-quinone methide (o-QM) is reported. The pairing of ambiphilic synthons in a complementary fashion is examined whereby o-fluorobenzenesulfonamides are merged with in situ generated o-QM in a formal [4 + 4] cyclization pathway to afford 5,2,1-dibenzooxathiazocine-2,2-dioxide scaffolds under microwave (mW) conditions. The method reported represents the first use of an o-QM in a formal hetero [4 + 4] cyclization.
    DOI:
    10.1021/ol100495w
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文献信息

  • A Formal [4 + 4] Complementary Ambiphile Pairing Reaction: A New Cyclization Pathway for <i>ortho</i>-Quinone Methides
    作者:Thiwanka B. Samarakoon、Moon Y. Hur、Ryan D. Kurtz、Paul R. Hanson
    DOI:10.1021/ol100495w
    日期:2010.5.21
    A formal, one-pot [4 + 4] cyclization pathway for the generation of eight-membered sultams via in situ generation of an ortho-quinone methide (o-QM) is reported. The pairing of ambiphilic synthons in a complementary fashion is examined whereby o-fluorobenzenesulfonamides are merged with in situ generated o-QM in a formal [4 + 4] cyclization pathway to afford 5,2,1-dibenzooxathiazocine-2,2-dioxide scaffolds under microwave (mW) conditions. The method reported represents the first use of an o-QM in a formal hetero [4 + 4] cyclization.
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