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8-[1,3]dithian-2-ylidene-1,4-dioxa-spiro[4,5]decane | 437716-30-8

中文名称
——
中文别名
——
英文名称
8-[1,3]dithian-2-ylidene-1,4-dioxa-spiro[4,5]decane
英文别名
8-(1,3-dithian-2-ylidene)-1,4-dioxaspiro[4.5]decane
8-[1,3]dithian-2-ylidene-1,4-dioxa-spiro[4,5]decane化学式
CAS
437716-30-8
化学式
C12H18O2S2
mdl
——
分子量
258.406
InChiKey
WDHGLFHFQIWGDH-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):
    2.2
  • 重原子数:
    16
  • 可旋转键数:
    0
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.83
  • 拓扑面积:
    69.1
  • 氢给体数:
    0
  • 氢受体数:
    4

反应信息

  • 作为反应物:
    描述:
    8-[1,3]dithian-2-ylidene-1,4-dioxa-spiro[4,5]decane 在 Pd EnCat 盐酸 、 sodium tetrahydroborate 、 乙醇三氟甲磺酸potassium carbonate丙酮 作用下, 以 1,4-二氧六环二氯甲烷 为溶剂, 反应 4.42h, 生成 (2R)-4-[4-{4-[difluoro(trans-4-hydroxycyclohexyl)methoxy]phenyl}-2-oxopyridin-1(2H)-yl]-2-methyl-2-(methylsulfonyl)-N-(tetrahydro-2H-pyran-2-yloxy)butanamide
    参考文献:
    名称:
    [EN] N-LINKED HYDROXAMIC ACID DERIVATIVES USEFUL AS ANTIBACTERIAL AGENTS
    [FR] DÉRIVÉS D'ACIDE HYDROXAMIQUE À LIAISON N, UTILES COMME AGENTS ANTIBACTÉRIENS
    摘要:
    本发明涉及一类新的羟肟酸衍生物,它们作为LpxC抑制剂的用途,更具体地用于治疗细菌感染。公式(I)。
    公开号:
    WO2011073845A1
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文献信息

  • N-Linked Hydroxamic Acid Derivatives Useful As Antibacterial Agents
    申请人:Brown Matthew Frank
    公开号:US20120258948A1
    公开(公告)日:2012-10-11
    The present invention is directed to a new class of hydroxamic acid derivatives of formula I, wherein the variables G, T, D, L, R 1 , R 2 , R 3 are as described herein, their use as LpxC inhibitors, and more specifically their use to treat bacterial infections in a patient in need thereof.
    本发明涉及一种新的羟肟酸衍生物类别,其化学式为I,其中变量G,T,D,L,R1,R2,R3如本文所述,其用作LpxC抑制剂,更具体地用于治疗有需要的患者的细菌感染。
  • N-linked hydroxamic acid derivatives useful as antibacterial agents
    申请人:Brown Matthew Frank
    公开号:US08664401B2
    公开(公告)日:2014-03-04
    The present invention is directed to a new class of hydroxamic acid derivatives of formula I, wherein the variables G, T, D, L, R1, R2, R3 are as described herein, their use as LpxC inhibitors, and more specifically their use to treat bacterial infections in a patient in need thereof.
    本发明涉及一种新的羟肟酸衍生物类别,其化学式为I,其中变量G、T、D、L、R1、R2、R3如本文所述,它们的用途是LpxC抑制剂,更具体地用于治疗患有细菌感染的患者。
  • N-Link Hydroxamic Acid Derivatives Useful As Antibacterial Agents
    申请人:Pfizer Inc.
    公开号:US20140128363A1
    公开(公告)日:2014-05-08
    The present invention is directed to a new class of hydroxamic acid derivatives, their use as LpxC inhibitors, and more specifically their use to treat bacterial infections.
    本发明涉及一种新的羟肟酸衍生物类,其用作LpxC抑制剂,更具体地用于治疗细菌感染。
  • N-link hydroxamic acid derivatives useful as antibacterial agents
    申请人:Pfizer Inc.
    公开号:US09018384B2
    公开(公告)日:2015-04-28
    The present invention is directed to a new class of hydroxamic acid derivatives, their use as LpxC inhibitors, and more specifically their use to treat bacterial infections.
    本发明涉及一种新型羟肟酸衍生物,其作为LpxC抑制剂的用途,更具体地用于治疗细菌感染。
  • US20140343031A1
    申请人:——
    公开号:——
    公开(公告)日:——
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