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2,3-dihydro-1-benzoxepin-4-carboxylic acid ethylester | 52187-00-5

中文名称
——
中文别名
——
英文名称
2,3-dihydro-1-benzoxepin-4-carboxylic acid ethylester
英文别名
ethyl 2,3-dihydrobenzoxepine-4-carboxylate;ethyl 2,3-dihydro-1-benzoxepine-4-carboxylate;ethyl 2,3-dihydrobenz[b]oxepine-4-carboxylate;2,3-Dihydro-4-(ethoxycarbonyl)-benzoxepine
2,3-dihydro-1-benzoxepin-4-carboxylic acid ethylester化学式
CAS
52187-00-5
化学式
C13H14O3
mdl
——
分子量
218.252
InChiKey
NLASQKUIXZSNAE-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:
    332.6±41.0 °C(predicted)
  • 密度:
    1.145±0.06 g/cm3(Temp: 20 °C; Press: 760 Torr)(predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    2.7
  • 重原子数:
    16
  • 可旋转键数:
    3
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.31
  • 拓扑面积:
    35.5
  • 氢给体数:
    0
  • 氢受体数:
    3

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

反应信息

  • 作为反应物:
    描述:
    盐酸胍2,3-dihydro-1-benzoxepin-4-carboxylic acid ethylestersodium methylate 作用下, 以 DMF (N,N-dimethyl-formamide) 为溶剂, 生成 N-(aminoiminomethyl)-2,3-dihydrobenz[b]oxepine-4-carboxamide
    参考文献:
    名称:
    Substituted guanidine derivatives and process for producing the same
    摘要:
    通式(1)所代表的化合物: 其中R1、R2、R3、R4和R5中的每一个是氢原子、烷基、取代烷基、烯基、炔基、环烷基、环烯基、饱和杂环基、芳香基、酰基或类似物;Y1、Y2、Y3和Y4中的每一个是单键、—CH2—、—O—、—CO—或类似物,前提是至少两个Y1到Y4中的独立团是单键以外的团;以及Z可以不存在,或者一个或多个Z可以存在且独立地是烷基、取代烷基、烯基、炔基、环烷基、环烯基、饱和杂环基、卤素原子、羧基、烷氧羰基、芳香基、酰基或类似物,对于由于钠/质子交换传输系统加速而引起的疾病,具有治疗或预防作用。
    公开号:
    US06369110B1
  • 作为产物:
    描述:
    4-(2-formylphenoxy)-butyric acid ethyl estersodium ethanolate 作用下, 以 乙醇碳酸二乙酯 为溶剂, 以61%的产率得到2,3-dihydro-1-benzoxepin-4-carboxylic acid ethylester
    参考文献:
    名称:
    Process for producing cyclic compound
    摘要:
    一种适用于安全批量生产用于药品、农药、食品、化妆品和化学产品或其中间体的环状化合物的过程,通过简短步骤。该过程用于生产由以下公式表示的化合物: 1 (其中Z代表一个吸电子基团;W代表可选择取代的乙烯或可选择取代的乙烯基;R 3 代表氢或可选择取代的碳氢基团;X代表二价基团[但当W代表可选择取代的乙烯基时,那么—X—CH 2 —Z不是—X 1 —X 2 —CH 2 —Z(其中X 1 代表硫或可选择取代的氮,X 2 代表可选择取代的乙烯基)]或其盐,其特征在于将由以下公式(II)或其盐表示的化合物: 2 (其中符号具有与上述相同的含义)置于含有碳酸二酯的溶剂中进行环闭合反应。
    公开号:
    US20030040632A1
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文献信息

  • Substituted guanidine derivatives and process for producing the same
    申请人:Sumitomo Pharmaceuticals Company
    公开号:US06369110B1
    公开(公告)日:2002-04-09
    A compound represented by the general formula (1): wherein each of R1, R2, R3, R4 and R5 is a hydrogen atom, an alkyl group, a substituted alkyl group, an alkenyl group, an alkynyl group, a cycloalkyl group, a cycloalkenyl group, a saturated heterocyclic group, an aromatic group, an acyl group or the like; each of Y1, Y2, Y3 and Y4 is a single bond, —CH2—, —O—, —CO— or the like, provided that at least two of Y1 through Y4 are independently a group other than a single bond; and Z may be absent, or one or more Zs may be present and are independently an alkyl group, a substituted alkyl group, an alkenyl group, an alkynyl group, a cycloalkyl group, a cycloalkenyl group, a saturated heterocyclic group, a halogen atom, a carboxyl group, an alkoxycarbonyl group, an aromatic group, an acyl group or the like, is useful as a therapeutic or prophylactic agent for diseases caused by the acceleration of the sodium/proton exchange transport system.
    通式(1)所代表的化合物: 其中R1、R2、R3、R4和R5中的每一个是氢原子、烷基、取代烷基、烯基、炔基、环烷基、环烯基、饱和杂环基、芳香基、酰基或类似物;Y1、Y2、Y3和Y4中的每一个是单键、—CH2—、—O—、—CO—或类似物,前提是至少两个Y1到Y4中的独立团是单键以外的团;以及Z可以不存在,或者一个或多个Z可以存在且独立地是烷基、取代烷基、烯基、炔基、环烷基、环烯基、饱和杂环基、卤素原子、羧基、烷氧羰基、芳香基、酰基或类似物,对于由于钠/质子交换传输系统加速而引起的疾病,具有治疗或预防作用。
  • Process for producing cyclic compound
    申请人:——
    公开号:US20030040632A1
    公开(公告)日:2003-02-27
    A process suitable for safely mass-producing, through a short step, cyclic compounds useful in medicines, agricultural chemicals, foods, cosmetics, and chemical products or as intermediates therefor. The process, which is for producing a compound represented by the formula: 1 {wherein Z represents an electron-attracting group; W represents optionally substituted ethylene or optionally substituted vinylene; R 3 represents hydrogen or an optionally substituted hydrocarbon group; and X represents a divalent group [provided that when W represents optionally substituted vinylene, then —X—CH 2 —Z is not —X 1 —X 2 —CH 2 —Z (wherein X 1 represents sulfur or optionally substituted nitrogen and X 2 represents optionally substituted ethylene)]} or a salt thereof, is characterized by subjecting a compound represented by the formula (II) or a salt thereof: 2 (wherein the symbols have the same meanings as the above) to a ring closure reaction in a solvent containing a carbonic diester.
    一种适用于安全批量生产用于药品、农药、食品、化妆品和化学产品或其中间体的环状化合物的过程,通过简短步骤。该过程用于生产由以下公式表示的化合物: 1 (其中Z代表一个吸电子基团;W代表可选择取代的乙烯或可选择取代的乙烯基;R 3 代表氢或可选择取代的碳氢基团;X代表二价基团[但当W代表可选择取代的乙烯基时,那么—X—CH 2 —Z不是—X 1 —X 2 —CH 2 —Z(其中X 1 代表硫或可选择取代的氮,X 2 代表可选择取代的乙烯基)]或其盐,其特征在于将由以下公式(II)或其盐表示的化合物: 2 (其中符号具有与上述相同的含义)置于含有碳酸二酯的溶剂中进行环闭合反应。
  • Benzopyrans and benzoxepines, pharmaceutical compositions comprising them and preparation process
    申请人:Merck Patent GmbH
    公开号:US06596758B1
    公开(公告)日:2003-07-22
    The present invention relates to benzopyrans and benzoxepines of formula (I), wherein X, A, R1, R2 and (R)p have the meanings as given in claim 1, which can be used in the treatment of dislipidaemias, atherosclerosis and diabetes, to pharmaceutical compositions comprising them and to processes allowing the preparation of these compounds.
    本发明涉及式(I)的苯并吡喃和苯并氧杂环庚三烯,其中X、A、R1、R2和(R)p具有权利要求1中所述的含义,可用于治疗血脂异常、动脉粥样硬化和糖尿病,涉及包含它们的药物组合物以及制备这些化合物的方法。
  • [EN] BENZOPYRANS AND BENZOXEPINES, PHARMACEUTICAL COMPOSITIONS COMPRISING THEM AND PREPARATION PROCESS<br/>[FR] BENZOPYRANES ET BENZOXEPINES PREPARATION PHARMACEUTIQUES LES INCLUANT ET LEUR PROCEDE D'OBTENTION
    申请人:MERCK PATENT GMBH
    公开号:WO2000039113A1
    公开(公告)日:2000-07-06
    The present invention relates to benzopyrans and benzoxepines of formula (I), wherein X, A, R1, R2 and (R)p have the meanings as given in claim 1, which can be used in the treatment of dislipidaemias, atherosclerosis and diabetes, to pharmaceutical compositions comprising them and to processes allowing the preparation of these compounds.
    本发明涉及公式(I)的苯并吡喃和苯并噁啶,其中X、A、R1、R2和(R)p的含义如权利要求书中所述,可用于治疗血脂异常、动脉粥样硬化和糖尿病,以及包含它们的制药组合物和制备这些化合物的过程。
  • NOVEL SUBSTITUTED GUANIDINE DERIVATIVES AND PROCESS FOR PRODUCING THE SAME
    申请人:Sumitomo Pharmaceuticals Company, Limited
    公开号:EP1083166A1
    公开(公告)日:2001-03-14
    Compounds represented by general formula (1) which are useful as remedies and preventives for diseases caused by acceleration in the sodium/proton exchange system, wherein R1, R2, R3, R4 and R5 represent each hydrogen, alkyl, substituted alkyl, alkenyl, alkynyl, cycloalkyl, cycloalkenyl, a saturated aromatic ring, acyl, etc.; Y1, Y2, Y3 and Y4 represent each a single bond, -CH2-, -O-, -CO-, etc., provided that at least two of Y1 to Y4 represent each a group other than a single bond; and Z may be absent or one or more Zs may be present and each represents alkyl, substituted alkyl, alkenyl, alkynyl, cycloalkyl, cycloalkenyl, a saturated aromatic ring, halogeno, carboxy, alkoxycarbonyl, an aromatic group, acyl, etc.
    通式(1)所代表的化合物,可作为钠/质子交换系统加速引起的疾病的治疗剂和预防剂,其中R1、R2、R3、R4和R5各自代表氢、烷基、取代烷基、烯基、炔基、环烷基、环烯基、饱和芳环、酰基等;Y1、Y2、Y3和Y4各自代表单键、-CH2-、-O-、-CO-等、条件是 Y1 至 Y4 中至少有两个分别代表单键以外的基团;Z 可以不存在,也可以存在一个或多个 Z,且各自代表烷基、取代烷基、烯基、炔基、环烷基、环烯基、饱和芳香环、卤素、羧基、烷氧羰基、芳香基、酰基等。
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