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6-[(5R)-5-(azidomethyl)-2-oxo-1,3-oxazolidin-3-yl]-4H-pyrido[3,2-b][1,4]oxazin-3-one

中文名称
——
中文别名
——
英文名称
6-[(5R)-5-(azidomethyl)-2-oxo-1,3-oxazolidin-3-yl]-4H-pyrido[3,2-b][1,4]oxazin-3-one
英文别名
——
6-[(5R)-5-(azidomethyl)-2-oxo-1,3-oxazolidin-3-yl]-4H-pyrido[3,2-b][1,4]oxazin-3-one化学式
CAS
——
化学式
C11H10N6O4
mdl
——
分子量
290.24
InChiKey
DTNJEUXGSNESKO-LURJTMIESA-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
  • 重原子数:
    21
  • 可旋转键数:
    3
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.36
  • 拓扑面积:
    95.1
  • 氢给体数:
    1
  • 氢受体数:
    7

文献信息

  • QUINAZOLINE-2,4-DIONE DERIVATIVES
    申请人:Hubschwerlen Christian
    公开号:US20140171425A1
    公开(公告)日:2014-06-19
    The invention relates to antibacterial compounds of formula (I), wherein R 1 is H, halogen, (C 1 -C 3 )alkyl or (C 1 -C 3 )alkoxy; R 2 is H, halogen, (C 1 -C 3 )alkyl, (C 1 -C 3 )alkoxy or pyrrolidin-1-yl; R 3 is H, halogen, (C 1 -C 3 )alkyl, (C 1 -C 3 )alkoxy, vinyl or 2-methoxycarbonyvinyl or R 2 and R 3 together with the two carbon atoms which bear them form a phenyl ring; R 4 is H, halogen, (C 1 -C 3 )alkyl or (C 1 -C 3 )alkoxy; and R 5 is H, (C 1 -C 3 )alkyl or cyclopropyl, or R 4 and R 5 form together a —CH 2 CH 2 CH 2 — group; A is the divalent group —CH 2 —, —CH 2 CH 2 —, #—CH(OH)CH 2 —*, #—CH 2 N(R 6 )—* and —CH 2 NHCH 2 —, wherein # indicates the point of attachment to the optionally substituted (quinazoline-2,4-dione-3-yl)methyl residue and * represents the point of attachment to the substituted (oxazolidinon-4-yl)methyl residue; R 6 is H or acetyl; Y is CH or N; and Q is O or S; and salts of such compounds.
    该发明涉及式(I)的抗菌化合物,其中R1为H、卤素、(C1-C3)烷基或(C1-C3)氧烷;R2为H、卤素、(C1-C3)烷基、(C1-C3)氧烷或吡咯烷-1-基;R3为H、卤素、(C1-C3)烷基、(C1-C3)氧烷、乙烯基或2-甲氧羰基乙烯基,或R2和R3与携带它们的两个碳原子一起形成苯环;R4为H、卤素、(C1-C3)烷基或(C1-C3)氧烷;R5为H、(C1-C3)烷基或环丙基,或R4和R5一起形成一个— —基团;A为二价基团—CH2—、— —、#—CH(OH) —*、#— N(R6)—*和— NH —,其中#表示可选择取代的(喹唑啉-2,4-二酮-3-基)甲基残基的连接点,*表示取代的(噁唑烷酮-4-基)甲基残基的连接点;R6为H或乙酰基;Y为CH或N;Q为O或S;以及这类化合物的盐。
  • [EN] OXAZOLIDINONE ANTIBIOTIC COMPOUNDS AND PROCESS OF PREPARATION<br/>[FR] COMPOSÉS ANTIBIOTIQUES D'OXAZOLIDINONE ET PROCÉDÉS DE PRÉPARATION
    申请人:BUGWORKS RES INDIA PVT LTD
    公开号:WO2019186590A1
    公开(公告)日:2019-10-03
    The present disclosure relates to compounds of Formula (I), its stereoisomers, pharmaceutically acceptable salts, complexes, hydrates, solvates, tautomers, polymorphs, racemic mixtures, optically active forms and pharmaceutically active derivative thereof and pharmaceutical compositions containing them as the active ingredient which can be used as medicaments. The aforementioned substances can also be used in the manufacture of medicaments for treatment, prevention, or suppression of diseases, and conditions mediated by microbes. The present disclosure also relates to the synthesis and characterization of aforementioned substances.
    本公开涉及式(I)的化合物,其立体异构体,药学上可接受的盐,络合物,合物,溶剂合物,互变异构体,多晶形,消旋混合物,光学活性形式及其药学活性衍生物,以及含有它们作为活性成分的药物组合物,可用作药物。上述物质还可用于制造用于治疗、预防或抑制由微生物介导的疾病和病况的药物。本公开还涉及上述物质的合成和表征。
  • Heterocyclic compounds useful as anti-bacterial agents and method for production thereof
    申请人:Bugworks Research, Inc.
    公开号:US10912780B2
    公开(公告)日:2021-02-09
    The present disclosure relates to compounds of Formula I, or their stereoisomers, pharmaceutically acceptable salts, complexes, hydrates, solvates, tautomers, polymorphs, racemic mixtures, optically active forms and pharmaceutically active derivatives thereof, and pharmaceutical compositions containing them as the active ingredient which can be used as medicaments. The aforementioned substances can also be used in the manufacture of medicaments for treatment, prevention or suppression of diseases, and conditions mediated by microbes. The present disclosure also relates to the synthesis and characterization of aforementioned substances.
    本公开涉及式 I 化合物或其立体异构体、药学上可接受的盐、络合物、合物、溶 液物、同系物、多晶型物、外消旋混合物、光学活性形式及其药学活性衍生物,以及含 有它们作为活性成分的可用作药物的药物组合物。上述物质还可用于制造治疗、预防或抑制由微生物介导的疾病和病症的药物。本公开还涉及上述物质的合成和表征。
  • HETEROCYCLIC COMPOUNDS USEFUL AS ANTI-BACTERIAL AGENTS AND METHOD FOR PRODUCTION THEREOF
    申请人:Bugworks Research, Inc.
    公开号:US20200085834A1
    公开(公告)日:2020-03-19
    The present disclosure relates to compounds of Formula I, or their stereoisomers, pharmaceutically acceptable salts, complexes, hydrates, solvates, tautomers, polymorphs, racemic mixtures, optically active forms and pharmaceutically active derivatives thereof, and pharmaceutical compositions containing them as the active ingredient which can be used as medicaments. The aforementioned substances can also be used in the manufacture of medicaments for treatment, prevention or suppression of diseases, and conditions mediated by microbes. The present disclosure also relates to the synthesis and characterization of aforementioned substances.
  • OXAZOLIDINONE ANTIBIOTIC COMPOUNDS AND PROCESS OF PREPARATION
    申请人:Bugworks Research, Inc.
    公开号:US20210008078A1
    公开(公告)日:2021-01-14
    The present disclosure relates to compounds of Formula I, its stereoisomers, pharmaceutically acceptable salts, complexes, hydrates, solvates, tautomers, polymorphs, racemic mixtures, optically active forms and pharmaceutically active derivative thereof and pharmaceutical compositions containing them as the active ingredient which can be used as medicaments. The aforementioned substances can also be used in the manufacture of medicaments for treatment, prevention, or suppression of diseases, and conditions mediated by microbes. The present disclosure also relates to the synthesis and characterization of aforementioned substances.
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