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5-[4-(2,3-dimethyl-naphtho[2,3-b]thiophen-4-yl)-2,6-diethyl-phenoxysulfonyl]-4-methoxy-thiophene-3-carboxylic acid

中文名称
——
中文别名
——
英文名称
5-[4-(2,3-dimethyl-naphtho[2,3-b]thiophen-4-yl)-2,6-diethyl-phenoxysulfonyl]-4-methoxy-thiophene-3-carboxylic acid
英文别名
5-[4-(2,3-dimethylbenzo[f][1]benzothiol-4-yl)-2,6-diethylphenoxy]sulfonyl-4-methoxythiophene-3-carboxylic acid
5-[4-(2,3-dimethyl-naphtho[2,3-b]thiophen-4-yl)-2,6-diethyl-phenoxysulfonyl]-4-methoxy-thiophene-3-carboxylic acid化学式
CAS
——
化学式
C30H28O6S3
mdl
——
分子量
580.747
InChiKey
HBQVPSLXZGGDNF-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):
    8.5
  • 重原子数:
    39
  • 可旋转键数:
    8
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.23
  • 拓扑面积:
    155
  • 氢给体数:
    1
  • 氢受体数:
    8

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:
    5-[4-(2,3-dimethyl-naphtho[2,3-b]thiophen-4-yl)-2,6-diethyl-phenoxysulfonyl]-4-methoxy-thiophene-3-carboxylic acid三溴化硼 作用下, 以 二氯甲烷 为溶剂, 以0.300 g (82%)的产率得到5-[4-(2,3-dimethyl-naphtho[2,3-b]thiophen-4-yl)-2,6-diethyl-phenoxysulfonyl]-4-hydroxy-thiophene-3-carboxylic acid
    参考文献:
    名称:
    Naphtho[2,3-B]heteroar-4-yl derivatives
    摘要:
    这项发明提供了具有结构的化合物,其中R.sup.1、R.sup.2、R.sup.3、R.sup.4、R.sup.5、W、R.sup.9、X、R.sup.6、p、Y、Z、R.sup.7和R.sub.8如规范中定义,或其药用盐,可用于治疗与胰岛素抵抗或高血糖相关的代谢紊乱。
    公开号:
    US06121271A1
  • 作为产物:
    描述:
    5-[4-(2,3-Dimethyl-naphtho[2,3-b]thiophen-4-yl)-2,6-diethyl-phenoxysulfonyl]-4-methoxy-thiophene-3-carboxylic acid methyl ester 、 氢氧化钾5-[4-(2,3-dimethyl-naphtho[2,3-b]thiophen-4-yl)-2,6-diethyl-phenoxysulfonyl]-4-methoxy-thiophene-3-carboxylic acid磷酸甲酯ethyl acetate n-hexane 作用下, 以to give 0.390 g (66%) of the title compound as a white solid, mp >230° C的产率得到5-[4-(2,3-dimethyl-naphtho[2,3-b]thiophen-4-yl)-2,6-diethyl-phenoxysulfonyl]-4-methoxy-thiophene-3-carboxylic acid
    参考文献:
    名称:
    Naphtho[2,3-B]heteroar-4-yl derivatives
    摘要:
    该发明提供了具有以下结构的I型化合物,其中R.sup.1、R.sup.2、R.sup.3、R.sup.4、R.sup.5、W、R.sup.9、X、R.sup.6、p、Y、Z、R.sup.7和R.sub.8如规范中所定义,或其药学上可接受的盐,其在治疗与胰岛素抵抗或高血糖相关的代谢紊乱方面具有用处。
    公开号:
    US06121271A1
  • 作为试剂:
    描述:
    5-[4-(2,3-Dimethyl-naphtho[2,3-b]thiophen-4-yl)-2,6-diethyl-phenoxysulfonyl]-4-methoxy-thiophene-3-carboxylic acid methyl ester 、 氢氧化钾5-[4-(2,3-dimethyl-naphtho[2,3-b]thiophen-4-yl)-2,6-diethyl-phenoxysulfonyl]-4-methoxy-thiophene-3-carboxylic acid磷酸甲酯ethyl acetate n-hexane 作用下, 以to give 0.390 g (66%) of the title compound as a white solid, mp >230° C的产率得到5-[4-(2,3-dimethyl-naphtho[2,3-b]thiophen-4-yl)-2,6-diethyl-phenoxysulfonyl]-4-methoxy-thiophene-3-carboxylic acid
    参考文献:
    名称:
    Naphtho[2,3-B]heteroar-4-yl derivatives
    摘要:
    该发明提供了具有以下结构的I型化合物,其中R.sup.1、R.sup.2、R.sup.3、R.sup.4、R.sup.5、W、R.sup.9、X、R.sup.6、p、Y、Z、R.sup.7和R.sub.8如规范中所定义,或其药学上可接受的盐,其在治疗与胰岛素抵抗或高血糖相关的代谢紊乱方面具有用处。
    公开号:
    US06121271A1
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文献信息

  • NAPHTHO[2,3-B]HETEROAR-4-YL DERIVATIVES
    申请人:AMERICAN HOME PRODUCTS CORPORATION
    公开号:EP1077968A1
    公开(公告)日:2001-02-28
  • US6121271A
    申请人:——
    公开号:US6121271A
    公开(公告)日:2000-09-19
  • [EN] NAPHTHO[2,3-B]HETEROAR-4-YL DERIVATIVES<br/>[FR] DERIVES DE NAPHTO[2,3-B]HETEROAR-4-YLE
    申请人:AMERICAN HOME PRODUCTS CORPORATION
    公开号:WO1999058522A1
    公开(公告)日:1999-11-18
    (EN) This invention provides compounds of structural Formula (I), wherein R1 and R2 are each, independently, hydrogen, nitrile, nitro, amino, alkylamino of 1-6 carbon atoms, dialkylamino of 1-6 carbon atoms per alkyl group, cycloalkylamino of 3-8 carbon atoms, alkyl of 1-6 carbon atoms, perfluoroalkyl of 1-6 carbon atoms, halogen, cycloalkyl of 3-8 carbon atoms, thienyl, furyl, phenyl or phenyl mono-, di-, or tri-substituted with halogen, hydroxy, alkyl of 1-6 carbon atoms, perfluoroalkyl of 1-6 carbon atoms, alkoxy of 1-6 carbon atoms, or perfluoroalkoxy of 1-6 carbon atoms; R3 and R4 are each, independently, hydrogen, alkyl of 1-6 carbon atoms, perfluoroalkyl of 1-6 carbon atoms, hydroxyalkyl of 1-6 carbon atoms, aminoalkyl of 1-6 carbon atoms, acyl of 2-7 carbon atoms; R5 is hydrogen, halogen, alkyl of 1-6 carbon atoms, perfluoroalkyl of 1-6 carbon atoms, nitrile, alkoxy of 1-6 carbon atoms, aryloxy, arylalcoxy of 2-12 carbon atoms, arylsulfanyl; W is S, O, or NR9; R9 is hydrogen or alkyl of 1-6 carbon atoms; X is O, -NR6-, or -(CH2)pNR6-; R6 is hydrogen, or alkyl of 1-6 carbon atoms; p is 1 to 4; Y is methylene, carbonyl, -SO2-, or -SO-; Z is phenyl, heteroaryl, or naphthyl; R7 and R8 are each, independently, hydrogen, carboxyl, acyl of 2-7 carbon atoms, hydroxyl, hydroxyalkyl of 1-6 carbon atoms, hydroxyalkanoyl of 1-6 carbon atoms, alkoxy of 1-6 carbon atoms, perfluoroalkoxy of 1-6 carbon atoms, alkoxycarbonyl of 2-7 carbon atoms, perfluoroalkoxycarbonyl of 2-7 carbon atoms, alkyl of 1-6 carbon atoms, perfluoroalkyl of 1-6 carbon atoms, aryl, aryloxy, aryloxycarbonyl, heteroaryloxycarbonyl, arylalkoxy of 6-12 carbon atoms, heteroaryl, alkanoyloxy of 1-6 carbon atoms, perfluoroalkanoyloxy of 1-6 carbon atoms, heteroaroyloxy, aroyloxy, tetrazolyl, mercapto, nitrile, amino, carbamoy, aminoalkyl of 1-6 carbon atoms, -NHSO2CF3, carboxyaldehyde, halogen, nitro, acylamino, or pyrimidyl optionally substituted with mercapto, 3-hydroxy-cyclobut-3-ene-4-yl-1,2-dione, or tetronic acid; or a pharmaceutically acceptable salt thereof, which are useful in treating metabolic disorders related to insulin resistance or hyperglycemia.(FR) L'invention concerne des composés de la formule structurelle (I) dans laquelle R1 et R2 représentent chacun indépendamment, hydrogène, nitrile, nitro, amino, alkylamino C1-6, dialkylamino comprenant 1 à 6 atomes de carbone par groupe alkyle, cycloalkyl-amino C3-8, alkyle C1-6, perfluoroalkyle C1-6, halogène, cycloalkyle C3-8, thiényle, furyle, phényle ou phényle mono-, di- ou tri-substitué par halogène, hydroxy, alkyle C1-6, perfluoroalkyle C1-6, alcoxy C1-6, ou perfluoroalcoxy C1-6; R3 et R4 représentent chacun indépendamment hydrogène, alkyle C1-6, perfluoroalkyle C1-6, hydroxyalkyle C1-6, aminoalkyle C1-6, acyle C2-7; R5 représente hydrogène, halogène, alkyle C1-6, perfluoroalkyle C1-6, nitrile, alcoxy C1-6, aryloxy, arylalcoxy C2-12, arylsulfanyle; W représente S, O ou NR9; R9 représente hydrogène ou alkyle C1-6, X représente O, -NR6-, ou (CH2)pNR6-; R6 représente hydrogène, ou alkyle C1-6; p vaut 1 à 4; Y représente méthylène, carbonyle, -SO2-, ou SO-; Z représente phényle, hétéroaryle ou naphtyle; R7 et R8 représentent chacun indépendamment hydrogène, carboxyle, acyle C2-7, hydroxyle, hydroxyalkyle C1-6, hydroxyalcanoyle C1-6, alcoxy C1-6, perfluoroalcoxy C1-6, alcoxycarbonyle C2-7, perfluoroalcoxycarbonyle C2-7, alkyle C1-6, perfluoroalkyle C1-6, aryle, aryloxy, aryloxycarbonyle, hétéroaryloxycarbonyle, arylalcoxy C6-12, héréroaryle, alcanoyloxy C1-6, perfluoroalcanoyloxy C1-6, hétéroaroyloxy, aroyloxy, tétrazolyle, mercapto, nitrile, amino, carbamoyle, aminoalkyle C1-6, -NHSO2CF3, carboxyaldéhyde, halogène, nitro, acylamino, ou pyrimidyle éventuellement substitué par mercapto, 3-hydroxy-cyclobut-3-ène-4-yl-1,2-dione, ou acide tétronique. L'invention concerne également des sels de ces composés, acceptables sur le plan pharmacologique. Ces sels et composés sont utiles dans le traitement de troubles métaboliques associés à l'insulinorésistance ou à l'hyperglycémie.
  • Naphtho[2,3-B]heteroar-4-yl derivatives
    申请人:American Home Products Corporation
    公开号:US06121271A1
    公开(公告)日:2000-09-19
    This invention provides compounds of Formula I having the structure wherein R.sup.1, R.sup.2, R.sup.3, R.sup.4, R.sup.5, W, R.sup.9, X, R.sup.6, p, Y, Z, R.sup.7, and R.sub.8 are as defined in the specification, or a pharmaceutically acceptable salt thereof, which are useful in treating metabolic disorders related to insulin resistance or hyperglycemia.
    这项发明提供了具有结构的化合物,其中R.sup.1、R.sup.2、R.sup.3、R.sup.4、R.sup.5、W、R.sup.9、X、R.sup.6、p、Y、Z、R.sup.7和R.sub.8如规范中定义,或其药用盐,可用于治疗与胰岛素抵抗或高血糖相关的代谢紊乱。
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