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6-(ethylsulfonyl)-2H-1,4-benzoxazin-3(4H)-one | 874774-43-3

中文名称
——
中文别名
——
英文名称
6-(ethylsulfonyl)-2H-1,4-benzoxazin-3(4H)-one
英文别名
6-ethanesulfonyl-4H-benzo[1,4]oxazin-3-one;6-ethylsulfonyl-4H-1,4-benzoxazin-3-one
6-(ethylsulfonyl)-2H-1,4-benzoxazin-3(4H)-one化学式
CAS
874774-43-3
化学式
C10H11NO4S
mdl
MFCD00798368
分子量
241.268
InChiKey
CLBHSYOAMTZTBM-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

物化性质

  • 沸点:
    509.6±50.0 °C(Predicted)
  • 密度:
    1.354±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    0.5
  • 重原子数:
    16
  • 可旋转键数:
    2
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.3
  • 拓扑面积:
    80.8
  • 氢给体数:
    1
  • 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:
    6-(ethylsulfonyl)-2H-1,4-benzoxazin-3(4H)-one 在 sodium hydride 、 三氟乙酸 作用下, 以 氯仿N,N-二甲基甲酰胺 为溶剂, 生成 4-(2-(4-aminopiperidin-1-yl)ethyl)-6-(ethylsulfonyl)-2H-benzo[b][1,4]oxazin-3(4H)-one
    参考文献:
    名称:
    Exploring Left-Hand-Side substitutions in the benzoxazinone series of 4-amino-piperidine bacterial type IIa topoisomerase inhibitors
    摘要:
    An SAR survey at the C-6 benzoxazinone position of a novel scaffold which inhibits bacterial type IIa topoisomerase demonstrates that a range of small electron donating groups (EDG) and electron withdrawing groups (EWG) are tolerated for antibacterial activity. Cyano was identified as a preferred substituent that affords good antibacterial potency while minimizing hERG cardiac channel activity. (C) 2011 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2011.06.126
  • 作为产物:
    参考文献:
    名称:
    Production Method of Nitrogen-Containing Fused Ring Compounds
    摘要:
    本发明提供了一种优越的化合物生产方法和优越的纯化方法,用于治疗或预防涉及尿酸的病理学,如高尿酸血症、痛风石、急性痛风性关节炎、慢性痛风性关节炎、痛风性肾脏、尿路结石、肾功能障碍、冠状动脉疾病、缺血性心脏病等。 [手段] 通过将以下式[3]所代表的化合物或其盐与以下式[4]所代表的化合物、其盐或其反应衍生物反应,可以制备以下式[2]所代表的化合物或其药用可接受的盐。此外,可以以工业上优越的可操作性进行以下式[2]所代表的化合物的结晶,并且可以获得以下式[2]所代表的化合物的高质量晶体。 其中每个符号如描述中所定义。
    公开号:
    US20080064871A1
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文献信息

  • Nitrogen-containing fused ring compounds and use thereof
    申请人:Hirata Kazuyuki
    公开号:US20070010670A1
    公开(公告)日:2007-01-11
    A URAT1 activity inhibitor containing a nitrogen-containing fused ring compound represented by the following formula [1]: wherein each symbol is as defined in the description. The present invention is useful for the prophylaxis or treatment of pathology showing involvement of uric acid, such as hyperuricemia, gouty tophus, acute gouty arthritis, chronic gouty arthritis, gouty kidney, urolithiasis, renal function disorder, coronary artery disease, ischemic heart disease and the like.
    一种包含氮含有融合环化合物的URAT1活性抑制剂,其化学式如下所示[1]: 其中每个符号如描述中所定义。本发明对于预防或治疗显示尿酸参与的病理学,如高尿酸血症、痛风石、急性痛风性关节炎、慢性痛风性关节炎、痛风性肾脏、尿路结石、肾功能障碍、冠状动脉疾病、缺血性心脏病等方面具有用处。
  • Pharmaceutical Compositions Comprising Nitrogen-Containing Fused Ring Coumpounds
    申请人:Miki Kazuki
    公开号:US20080305169A1
    公开(公告)日:2008-12-11
    [Problems] The present invention provides pharmaceutical composition which is effective for the prophylaxis or treatment of pathology showing involvement of uric acid (hyperuricemia, gouty tophus, acute gout arthritis, chronic gout arthritis, gouty kidney, urolithiasis, renal function disorder, coronary arterial disease, ischemic heart disease and the like) and the like, and is superior in the time-course stability and dissolution property (disintegration property). [Solving Means] The pharmaceutical composition of the present invention is a pharmaceutical composition comprising a nitrogen-containing fused ring compound represented by the following formula [1] or a pharmaceutically acceptable salt thereof, and one or more pharmaceutically acceptable additives, wherein the nitrogen-containing fused ring compound or a pharmaceutically acceptable salt thereof is not in contact with a basic additive: wherein each symbol is as described in the specification.
    本发明提供了一种药物组合物,用于预防或治疗涉及尿酸的病理(高尿酸血症、痛风石、急性痛风性关节炎、慢性痛风性关节炎、痛风性肾脏、尿路结石、肾功能障碍、冠状动脉疾病、缺血性心脏病等),并且在时间稳定性和溶解性(分解性)方面具有优越性。 【解决手段】本发明的药物组合物是一种药物组合物,包括下式【1】所表示的含氮融合环化合物或其药学上可接受的盐,以及一种或多种药学上可接受的添加剂,其中所述的含氮融合环化合物或其药学上可接受的盐与碱性添加剂不接触: 其中每个符号如说明书中所述。
  • Compounds for the treatment of multi-drug resistant bacterial infections
    申请人:AstraZeneca AB
    公开号:US07875715B2
    公开(公告)日:2011-01-25
    The present invention relates to compounds that demonstrate antibacterial activity, processes for their preparation, pharmaceutical compositions containing them as the active ingredient, to their use as medicaments and to their use in the manufacture of medicaments for use in the treatment of bacterial infections in warm-blooded animals such as humans. In particular this invention relates to compounds useful for the treatment of bacterial infections in warm-blooded animals such as humans, more particularly to the use of these compounds in the manufacture of medicaments for use in the treatment of bacterial infections in warm-blooded animals such as humans.
    本发明涉及表现出抗菌活性的化合物,其制备过程,含有其作为活性成分的药物组合物,以及它们作为药物的使用和用于制造用于治疗温血动物(如人类)细菌感染的药物的使用。特别地,本发明涉及用于治疗温血动物(如人类)细菌感染的有用化合物,更具体地涉及这些化合物用于制造用于治疗温血动物(如人类)细菌感染的药物。
  • COMPOUNDS FOR THE TREATMENT OF MULTI-DRUG RESISTANT BACTERIAL INFECTIONS
    申请人:Breault Gloria
    公开号:US20110092495A1
    公开(公告)日:2011-04-21
    The present invention relates to compounds that demonstrate antibacterial activity, processes for their preparation, pharmaceutical compositions containing them as the active ingredient, to their use as medicaments and to their use in the manufacture of medicaments for use in the treatment of bacterial infections in warm-blooded animals such as humans. In particular this invention relates to compounds useful for the treatment of bacterial infections in warm-blooded animals such as humans, more particularly to the use of these compounds in the manufacture of medicaments for use in the treatment of bacterial infections in warm-blooded animals such as humans.
    本发明涉及表现出抗菌活性的化合物,其制备过程,含有它们作为活性成分的制药组合物,它们作为药物的使用以及它们在制造用于治疗温血动物(如人类)细菌感染的药物中的使用。特别是本发明涉及用于治疗温血动物(如人类)细菌感染的有用化合物,更具体地涉及这些化合物在制造用于治疗温血动物(如人类)细菌感染的药物中的使用。
  • NITROGEN-CONTAINING FUSED RING COMPOUND AND USE THEREOF
    申请人:Japan Tobacco, Inc.
    公开号:EP1820515A1
    公开(公告)日:2007-08-22
    A URAT1 activity inhibitor containing a nitrogen-containing fused ring compound represented by the following formula [1]: wherein each symbol is as defined in the description. The present invention is useful for the prophylaxis or treatment of pathology showing involvement of uric acid, such as hyperuricemia, gouty tophus, acute gouty arthritis, chronic gouty arthritis, gouty kidney, urolithiasis, renal function disorder, coronary artery disease, ischemic heart disease and the like.
    一种 URAT1 活性抑制剂,含有下式[1]代表的含氮融合环化合物: 其中各符号如描述中所定义。本发明可用于预防或治疗尿酸参与的病变,如高尿酸血症、痛风性头痛、急性痛风性关节炎、慢性痛风性关节炎、痛风性肾、尿路结石、肾功能紊乱、冠状动脉疾病、缺血性心脏病等。
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