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3-(2-hydroxyethyl)-6-nitro4-oxo-3,4-dihydro-1,3-benzoxazine | 159691-59-5

中文名称
——
中文别名
——
英文名称
3-(2-hydroxyethyl)-6-nitro4-oxo-3,4-dihydro-1,3-benzoxazine
英文别名
3-(2-hydroxyethyl)-6-nitro-2H-1,3-benzoxazin-4-one
3-(2-hydroxyethyl)-6-nitro4-oxo-3,4-dihydro-1,3-benzoxazine化学式
CAS
159691-59-5
化学式
C10H10N2O5
mdl
——
分子量
238.2
InChiKey
ODOYCXAMHYTYIP-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):
    0.4
  • 重原子数:
    17
  • 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:
    95.6
  • 氢给体数:
    1
  • 氢受体数:
    5

上下游信息

  • 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:
    diisopropyl diazodicarboxylate3-(2-hydroxyethyl)-6-nitro4-oxo-3,4-dihydro-1,3-benzoxazine2-乙氧基-3-对羟基苯基丙酸乙酯三苯基膦 作用下, 以41.5%的产率得到(+/-)-ethyl 2-ethoxy-3-[4-[2-[6-nitro-4-oxo-3,4-dihydro-1,3-benzoxazin-3-yl]ethoxy]phenyl]propanoate
    参考文献:
    名称:
    Benzothiazin and benzoxazin derivatives; their preparation and uses
    摘要:
    本发明涉及新型抗肥胖和降胆固醇化合物,它们的衍生物,类似物,互变异构体,立体异构体,多晶形态,药学上可接受的盐,药学上可接受的溶剂合物以及含有它们的药学上可接受的组合物。更具体地说,本发明涉及一般式(I)的新型β-芳基-α-氧基取代烷基羧酸,其衍生物,类似物,互变异构体,立体异构体,多晶形态,药学上可接受的盐,药学上可接受的溶剂合物以及含有它们的药学上可接受的组合物。
    公开号:
    US06130214A1
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文献信息

  • [EN] NOVEL HETEROCYCLIC COMPOUNDS AND THEIR USE IN MEDICINE, PROCESS FOR THEIR PREPARATION AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM<br/>[FR] NOUVELLES COMPOSITIONS HETEROCYCLIQUES ET LEUR UTILISATION EN MEDECINE; PROCEDES DE LEUR FABRICATION ET COMPOSITIONS PHARMACEUTIQUES LES CONTENANT
    申请人:DR. REDDY'S RESEARCH FOUNDATION
    公开号:WO1999016758A1
    公开(公告)日:1999-04-08
    (EN) The present invention relates to novel antiobesity and hypocholesterolemic compounds, their derivatives, their analogs, their tautomeric forms, their stereisomers, their polymorphs, their pharmaceutically acceptable salts, their pharmaceutically acceptable solvates and pharmaceutically acceptable compositions containing them. More particularly, the present invention relates to novel $g(b)-aryl-$g(a)-oxysubstituted alkylcarboxylic acids of general formula (I), their derivatives, their analogs, their tautomeric forms, their stereosomers, their polymorphs, their pharmaceutically acceptable salts, their pharmaceutically acceptable solvates and pharmaceutically acceptable compositions containing them.(FR) La présente invention concerne de nouveaux composés anti-obésité et hypocholestérolémiques, leurs dérivés, analogues, formes tautomères, stéréoisomères, polymorphes, sels pharmaceutiquement acceptables, solvates pharmaceutiquement acceptables et des compositions pharmaceutiquement acceptables les contenant. Plus particulièrement, cette invention se rapporte à de nouveaux acides alkylcarboxyliques $g(b)-aryl-$g(a)-oxysubstitués qui correspondent à la formule générale (I), ainsi qu'à leurs dérivés, analogues, formes tautomères, stéréoisomères, polymorphes, sels pharmaceutiquement acceptables, solvates pharmaceutiquement acceptables et à des compositions pharmaceutiquement acceptables les contenant.
    本发明涉及新型抗肥胖和降低胆固醇化合物,其衍生物,类似物,互变异构体,立体异构体,多晶形态,药学上可接受的盐,药学上可接受的溶剂化物和包含它们的药学上可接受的组合物。更具体地说,本发明涉及一般式(I)的新型$g(b)-芳基-$g(a)-氧基取代的烷基羧酸,其衍生物,类似物,互变异构体,立体异构体,多晶形态,药学上可接受的盐,药学上可接受的溶剂化物和包含它们的药学上可接受的组合物。
  • Novel heterocyclic compounds and their use in medicine; process for their preparation and pharmaceutical compositions containing them
    申请人:DR. REDDY'S RESEARCH FOUNDATION & REDDY-CHEMINOR INC.
    公开号:US20010027198A1
    公开(公告)日:2001-10-04
    The present invention relates to novel antiobesity and hypocholesterolemic compounds, their derivatives, their analogs, their tautomeric forms, their stereoisomers, their polymorphs, their pharmaceutically acceptable salts, their pharmaceutically acceptable solvates and pharmaceutically acceptable compositions containing them. More particularly, the present invention relates to novel &bgr;-aryl-&agr;-oxysubstituted alkylcarboxylic acids of the general formula (1), their derivatives, their analogs, their tautomeric forms, their stereosomers, their polymorphs, their pharmaceutically acceptable salts, their pharmaceutically acceptable solvates and pharmaceutically acceptable compositions containing them. 1 The present invention also relates to a process for the preparation of the above said novel compounds, their analogs, their derivatives, their tautomeric forms, their stereoisomers, their polymorphs, their pharmaceutically acceptable salts, pharmaceutically acceptable solvates, novel intermediates and pharmaceutical compositions containing them.
    本发明涉及新型抗肥胖和降胆固醇化合物、它们的衍生物、类似物、互变异构体、立体异构体、多晶形态、药学上可接受的盐、药学上可接受的溶剂及含有它们的药学上可接受的组合物。更具体地,本发明涉及一般式(1)的新型β-芳基-α-氧基取代烷基羧酸、它们的衍生物、类似物、互变异构体、立体异构体、多晶形态、药学上可接受的盐、药学上可接受的溶剂及含有它们的药学上可接受的组合物。本发明还涉及制备上述新型化合物、类似物、衍生物、互变异构体、立体异构体、多晶形态、药学上可接受的盐、药学上可接受的溶剂、新型中间体和含有它们的制药组合物的方法。
  • Benzoazine derivative or salt thereof and pharmaceutical composition comprising the same
    申请人:SS Pharmaceutical Co., Ltd.
    公开号:EP0787727A1
    公开(公告)日:1997-08-06
    A benzoazine derivative represented by the following formula (1),    wherein R1 represents an alkyl group, alkoxy group, halogen atom, halogenoalkyl group, amino group, hydroxy group, benzyloxy group which may have a substituent, cyano group, carbamoyl group, acyl group, nitro group, carboxy group, or sulfonamide group; R2 and R3 may be the same or different and each individually represents a hydrogen atom or an alkyl group, or R2 and R3 indicate in combination an alkylene group having 2-7 carbon atoms; R4 and R5 may be the same or different and each individually represents a hydrogen atom or an alkyl group; X denotes O, S, or N-R6 (wherein R6 represents a hydrogen atom, an alkyl group, or an aryl group or pyridyl group which may have a substituent); m is an integer from 0 to 4; and n is an integer from l to 3, or a salt of the benzoazine derivative. The compound exhibits superior effects for reducing blood glucose value, plasma insulin value, and plasma triglyceride value, and is useful as a medicament for preventing or treating diabetes, hyperlipidemia, and obesity.
    由下式(1)代表的苯并嗪衍生物、 其中 R1 代表烷基、烷氧基、卤素原子、卤代烷基、氨基、羟基、可能具有取代基的苄氧基、氰基、氨基甲酰基、酰基、硝基、羧基或磺酰胺基;R2 和 R3 可以相同或不同,各自单独代表氢原子或烷基,或 R2 和 R3 组合表示具有 2-7 个碳原子的亚烷基;R4和R5可以相同或不同,各自代表氢原子或烷基;X表示O、S或N-R6(其中R6代表氢原子、烷基或芳基或吡啶基,可具有取代基);m是0至4的整数;n是l至3的整数,或苯并嗪衍生物的盐。该化合物在降低血糖值、血浆胰岛素值和血浆甘油三酯值方面表现出卓越的效果,可用作预防或治疗糖尿病、高脂血症和肥胖症的药物。
  • NOVEL HETEROCYCLIC COMPOUNDS AND THEIR USE IN MEDICINE, PROCESS FOR THEIR PREPARATION AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM
    申请人:DR. REDDY'S RESEARCH FOUNDATION
    公开号:EP1124807A1
    公开(公告)日:2001-08-22
  • US5710152A
    申请人:——
    公开号:US5710152A
    公开(公告)日:1998-01-20
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