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1-(2-(4-((2,3-dihydro(1,4)dioxino(2,3-c)pyridin-7-ylmethyl)amino)-3-fluoropiperidin-1-yl)ethyl)-7-methoxyquinoxalin-2(1H)-one | 917832-70-3

中文名称
——
中文别名
——
英文名称
1-(2-(4-((2,3-dihydro(1,4)dioxino(2,3-c)pyridin-7-ylmethyl)amino)-3-fluoropiperidin-1-yl)ethyl)-7-methoxyquinoxalin-2(1H)-one
英文别名
1-[2-[4-(2,3-dihydro-[1,4]dioxino[2,3-c]pyridin-7-ylmethylamino)-3-fluoropiperidin-1-yl]ethyl]-7-methoxyquinoxalin-2-one
1-(2-(4-((2,3-dihydro(1,4)dioxino(2,3-c)pyridin-7-ylmethyl)amino)-3-fluoropiperidin-1-yl)ethyl)-7-methoxyquinoxalin-2(1H)-one化学式
CAS
917832-70-3
化学式
C24H28FN5O4
mdl
——
分子量
469.516
InChiKey
ZGGXASXXNNQBCO-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):
    1.3
  • 重原子数:
    34
  • 可旋转键数:
    7
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.46
  • 拓扑面积:
    88.5
  • 氢给体数:
    1
  • 氢受体数:
    9

反应信息

  • 作为反应物:
    描述:
    1-(2-(4-((2,3-dihydro(1,4)dioxino(2,3-c)pyridin-7-ylmethyl)amino)-3-fluoropiperidin-1-yl)ethyl)-7-methoxyquinoxalin-2(1H)-one 、 ethyl acetate hydrochloride 在 乙醚 作用下, 以 乙酸乙酯 为溶剂, 以to give 25 mg of 1-(2-(4-((2,3-dihydro(1,4)dioxino(2,3-c)pyridin-7-ylmethyl)amino)-3-fluoropiperidin-1-yl)ethyl)-7-methoxyquinoxalin-2(1H)-one hydrochloride as a pale brown solid的产率得到1-(2-(4-((2,3-dihydro(1,4)dioxino(2,3-c)pyridin-7-ylmethyl)amino)-3-fluoropiperidin-1-yl)ethyl)-7-methoxyquinoxalin-2(1H)-one hydrochloride
    参考文献:
    名称:
    Quinoxalinones as antibacterial composition
    摘要:
    一种含氮杂环化合物或其药学上可接受的盐,其通式表示如下:具有强效的抗菌活性和高度安全性。因此,这些化合物可用作抗革兰氏阳性菌、抗革兰氏阴性菌和抗药性菌的抗菌剂。
    公开号:
    US08329694B2
  • 作为产物:
    描述:
    cis(+/-)-benzyl N-benzyl-[3-fluoropiperidin-4-yl]carbamate 在 20 % Pd(OH)2/C 、 四丁基氟化铵氢气三乙酰氧基硼氢化钠 、 sodium hydride 、 caesium carbonate三乙胺 作用下, 以 四氢呋喃甲醇二氯甲烷氯仿N,N-二甲基甲酰胺乙腈 为溶剂, 反应 32.0h, 生成 1-(2-(4-((2,3-dihydro(1,4)dioxino(2,3-c)pyridin-7-ylmethyl)amino)-3-fluoropiperidin-1-yl)ethyl)-7-methoxyquinoxalin-2(1H)-one
    参考文献:
    名称:
    具有降低的p K a的II型细菌拓扑异构酶的新型N-连接氨基哌啶抑制剂:具有改进的安全性的抗菌剂
    摘要:
    新型的细菌II型拓扑异构酶的非氟喹诺酮抑制剂(DNA促旋酶和拓扑异构酶IV)对于开发不受靶标介导的氟喹诺酮类交叉耐药性影响的新型抗菌剂具有重要意义。N-连接的氨基哌啶,例如7a,通常显示出强效的抗菌活性,包括对喹诺酮类耐药菌的隔离,但在体内受到hERG抑制作用(7a的IC 50 = 44μM)和QT延长。现在我们公开了以下发现,即新的类似物7a中具有降低的p ķ一个由于与取代在哌啶部分的吸电子取代基,如- [R ,小号-在图7c中,保留了7a的革兰氏阳性活性,但是显示出显着较少的hERG抑制(对于R,S - 7c,IC 50 = 233μM)。该化合物在狗中表现出中等清除率,在小鼠感染模型中有望对抗MRSA毒株,并且在豚鼠体内模型中测得的体内QT曲线得到改善。由于其有希望的活性,R,S -7c已进入I期临床研究。
    DOI:
    10.1021/jm300690s
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文献信息

  • 2-QUINOLINONE AND 2-QUINOXALINONE-DERIVATIVES AND THEIR USE AS ANTIBACTERIAL AGENTS
    申请人:Godfrey Andrew Aydon
    公开号:US20120270864A1
    公开(公告)日:2012-10-25
    The present invention relates to compounds of Formula (I): and pharmaceutically acceptable salts thereof, to their use in the treatment of bacterial infections, and to their methods of preparation.
    本发明涉及公式(I)化合物及其药学上可接受的盐,以及它们在治疗细菌感染方面的用途和制备方法。
  • NOVEL NITROGENATED HETEROCYCLIC COMPOUND AND SALT THEREOF
    申请人:Kiyoto Taro
    公开号:US20100168418A1
    公开(公告)日:2010-07-01
    A nitrogen-containing heterocyclic compound represented by the general formula: wherein the dashed line represents a single bond or a double bond; R 1 , R 2 , R 3 , R 4 and R 5 independently represent a hydrogen atom, halogen atom, a lower alkyl, aryl, lower alkoxy or monocyclic heterocyclic group which may be substituted or the like; R 6 represents a lower alkyl, aryl, monocyclic heterocyclic, bicyclic heterocyclic or tricyclic heterocyclic group which may be substituted; X 1 represents a lower alkylene group or the like; X 2 represents a lower alkylene, lower alkenylene or lower alkynylene group which may be substituted; X 3 represents an oxygen atom, sulfur atom, a sulfinyl group, sulfonyl group or the like; Y 1 represents a bivalent cyclic group, containing a nitrogen, which may be substituted or the like; and Z 1 represents a nitrogen atom, a carbon atom which may be substituted or the like, or a salt thereof. The compound or salt has a potent antibacterial activity and a high safety, and is therefore useful as an excellent antibacterial agent.
    一种含氮杂环化合物,通式如下:其中虚线代表单键或双键;R1、R2、R3、R4和R5分别独立地代表氢原子、卤素原子、较低的烷基、芳基、较低的烷氧基或可以被取代的单环杂环基等;R6代表较低的烷基、芳基、单环杂环、双环杂环或三环杂环基,可以被取代;X1代表较低的烷基亚基或类似物;X2代表可以被取代的较低烷基、较低烯基或较低炔基亚基;X3代表氧原子、硫原子、亚砜基、磺酰基或类似物;Y1代表含有氮的二价环状基团,可以被取代或类似物;Z1代表氮原子、可以被取代的碳原子或类似物,或其盐。该化合物或盐具有强效的抗菌活性和高度的安全性,因此可用作优良的抗菌剂。
  • QUINOLINONES AND QUINOXALINONES AS ANTIBACTERIAL COMPOSITION
    申请人:KIYOTO Taro
    公开号:US20120214990A1
    公开(公告)日:2012-08-23
    A nitrogen-containing heterocyclic compound or pharmaceutically acceptable salt thereof represented by the general formula: which have a potent antibacterial activity and a high safety. Thus, the compounds are useful as antibacterial agents against gram-positive bacteria, gram-negative bacteria and drug resistant bacteria.
    一种含氮杂环化合物,或其药学上可接受的盐,其通式如下:具有强效的抗菌活性和高安全性。因此,这些化合物可用作抗革兰阳性菌、抗革兰阴性菌和抗药性菌的抗菌剂。
  • Quinoxalinones as antibacterial composition
    申请人:Toyama Chemical Co., Ltd.
    公开号:US08329694B2
    公开(公告)日:2012-12-11
    A nitrogen-containing heterocyclic compound or pharmaceutically acceptable salt thereof represented by the general formula: which have a potent antibacterial activity and a high safety. Thus, the compounds are useful as antibacterial agents against gram-positive bacteria, gram-negative bacteria and drug resistant bacteria.
    一种含氮杂环化合物或其药学上可接受的盐,其通式表示如下:具有强效的抗菌活性和高度安全性。因此,这些化合物可用作抗革兰氏阳性菌、抗革兰氏阴性菌和抗药性菌的抗菌剂。
  • Nitrogen-containing bicyclic compounds useful as antibacterial agents
    申请人:Toyama Chemical Co., Ltd.
    公开号:EP2468743A1
    公开(公告)日:2012-06-27
    A nitrogen-containing heterocyclic compound represented by the general formula: wherein the dashed line represents a single bond or a double bond; R1, R2, R3, R4 and R5 independently represent a hydrogen atom, halogen atom, a lower alkyl, aryl, lower alkoxy or monocyclic heterocyclic group which may be substituted or the like; R6 represents a lower alkyl, aryl, monocyclic heterocyclic, bicyclic heterocyclic or tricyclic heterocyclic group which may be substituted; X1 represents a lower alkylene group or the like; X2 represents a lower alkylene, lower alkenylene or lower alkynylene group which may be substituted; X3 represents an oxygen atom, sulfur atom, a sulfinyl group, sulfonyl group or the like; Y1 represents a bivalent cyclic group, containing a nitrogen, which may be substituted or the like; and Z1 represents a nitrogen atom, a carbon atom which may be substituted or the like, or a salt thereof. The compound or salt has a potent antibacterial activity and a high safety, and is therefore useful as an excellent antibacterial agent.
    一种由通式表示的含氮杂环化合物:其中虚线代表单键或双键;R1、R2、R3、R4和R5独立地代表氢原子、卤素原子、低级烷基、芳基、低级烷氧基或可被取代的单环杂环基团或类似基团;R6代表可被取代的低级烷基、芳基、单环杂环基团、双环杂环基团或三环杂环基团;X1代表低级亚烷基或类似基团;X2 代表可被取代的低级亚烷基、低级亚烯基或低级亚炔基; X3 代表氧原子、硫原子、亚砜基、磺酰基或类似物; Y1 代表可被取代的含氮的二价环基或类似物; Z1 代表氮原子、可被取代的碳原子或类似物,或其盐。该化合物或其盐具有很强的抗菌活性和很高的安全性,因此可用作优良的抗菌剂。
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