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ethyl 7-chloro-2,3-dihydro-6-hydroxy-5-propionylbenzofuran-2-carboxylate | 90246-86-9

中文名称
——
中文别名
——
英文名称
ethyl 7-chloro-2,3-dihydro-6-hydroxy-5-propionylbenzofuran-2-carboxylate
英文别名
ethyl 7-chloro-6-hydroxy-5-propanoyl-2,3-dihydro-1-benzofuran-2-carboxylate
ethyl 7-chloro-2,3-dihydro-6-hydroxy-5-propionylbenzofuran-2-carboxylate化学式
CAS
90246-86-9
化学式
C14H15ClO5
mdl
——
分子量
298.723
InChiKey
FYCOCALCWSGGMB-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:
    442.0±45.0 °C(Predicted)
  • 密度:
    1.344±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    3.2
  • 重原子数:
    20
  • 可旋转键数:
    5
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.43
  • 拓扑面积:
    72.8
  • 氢给体数:
    1
  • 氢受体数:
    5

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
  • 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:
    ethyl 7-chloro-2,3-dihydro-6-hydroxy-5-propionylbenzofuran-2-carboxylate吡啶sodium hydroxide盐酸羟胺 作用下, 反应 9.0h, 生成 7-Chloro-6-hydroxy-5-{1-[(E)-hydroxyimino]-propyl}-2,3-dihydro-benzofuran-2-carboxylic acid
    参考文献:
    名称:
    Substituted 5,6-dihydrofuro[3,2-f]-1,2-benzisoxazole-6-carboxylic acids: high-ceiling diuretics with uricosuric activity
    摘要:
    A series of substituted 5,6-dihydrofuro[3,2-f]-1,2-benzisoxazoles was prepared and evaluated for their saluretic and uricosuric properties. Pharmacological evaluation of the title compounds was carried out in mice, rats, dogs, and monkeys. The diuretic/saluretic nature of these compounds was observed in all species, whereas the uricosuric activity was best seen in the Cebus monkey. Evaluation of the enantiomers of 8-chloro-3-(o-fluorophenyl)-5,6-dihydrofuro [3,2-f]-1,2-benzisoxazole-6-carboxylic acid (15k) revealed that only the (+) enantiomer (29) displayed diuretic and saluretic activity, whereas both enantiomers possessed uricosuric activity. X-ray analysis showed that the (-) enantiomer (30) possesses the 2R configuration.
    DOI:
    10.1021/jm00374a014
  • 作为产物:
    描述:
    diethyl 7-chloro-2,3-dihydro-3-hydroxy-6-methoxybenzofuran-2,2-dicarboxylate 在 palladium on activated charcoal 三氯化铝硫酸氢气二甲基亚砜lithium chloride 作用下, 以 溶剂黄1461,2-二氯乙烷 为溶剂, 25.0 ℃ 、303.98 kPa 条件下, 反应 4.0h, 生成 ethyl 7-chloro-2,3-dihydro-6-hydroxy-5-propionylbenzofuran-2-carboxylate
    参考文献:
    名称:
    Substituted 5,6-dihydrofuro[3,2-f]-1,2-benzisoxazole-6-carboxylic acids: high-ceiling diuretics with uricosuric activity
    摘要:
    A series of substituted 5,6-dihydrofuro[3,2-f]-1,2-benzisoxazoles was prepared and evaluated for their saluretic and uricosuric properties. Pharmacological evaluation of the title compounds was carried out in mice, rats, dogs, and monkeys. The diuretic/saluretic nature of these compounds was observed in all species, whereas the uricosuric activity was best seen in the Cebus monkey. Evaluation of the enantiomers of 8-chloro-3-(o-fluorophenyl)-5,6-dihydrofuro [3,2-f]-1,2-benzisoxazole-6-carboxylic acid (15k) revealed that only the (+) enantiomer (29) displayed diuretic and saluretic activity, whereas both enantiomers possessed uricosuric activity. X-ray analysis showed that the (-) enantiomer (30) possesses the 2R configuration.
    DOI:
    10.1021/jm00374a014
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文献信息

  • 3-Alkyl-8-chloro-5,6-dihydrofuro-[3,2-f]-1,2-benzisoxazole-6-carboxylic
    申请人:Abbott Laboratories
    公开号:US04560558A1
    公开(公告)日:1985-12-24
    Disclosed are compounds of the formula: ##STR1## wherein X is hydrogen, loweralkyl, loweralkoxy or halo, Y is hydroxymethyl, carboxyl, carboxamido or carboloweralkoxy, and R is cyclohexyl, benzyl, norbornyl, loweralkyl, or a pharmaceutically acceptable salt thereof. The compounds are effective as diuretic agents.
    本发明涉及一种化合物,其化学式为:##STR1##其中X为氢、低碳基、低碳氧基或卤素,Y为羟甲基、羧基、羧酰胺基或羟基低碳氧基,R为环己基、苄基、去氢萘基、低碳基或其药学上可接受的盐。该化合物可作为利尿剂。
  • 3-Alkyl-8-chloro-5,6-dihydrofuro-[3,2-f]-1,2-benzisoxazole-6-carboxylic acids
    申请人:ABBOTT LABORATORIES
    公开号:EP0126342A2
    公开(公告)日:1984-11-28
    Disclosed are compounds of the formula: wherein X is hydrogen, loweralkyl, loweralkoxy or halo, Y is hydroxymethyl, carboxyl, carboxamido or carboloweralkoxy, and R is cyclohexyl, benzyl, norbornyl, loweralkyl, or a pharmaceutically acceptable salt thereof. The compounds are effective as diuretic agents.
    公开了式中的化合物:其中 X 是氢、低级烷基、低级烷氧基或卤代,Y 是羟甲基、羧基、羧酰胺基或碳低级烷氧基,R 是环己基、苄基、降冰片基、低级烷基或其药学上可接受的盐。 这些化合物是有效的利尿剂。
  • PARKS, J. A.;PLATTNER, J. J.
    作者:PARKS, J. A.、PLATTNER, J. J.
    DOI:——
    日期:——
  • US4560558A
    申请人:——
    公开号:US4560558A
    公开(公告)日:1985-12-24
  • Substituted 5,6-dihydrofuro[3,2-f]-1,2-benzisoxazole-6-carboxylic acids: high-ceiling diuretics with uricosuric activity
    作者:Jacob J. Plattner、Anthony K. L. Fung、James A. Parks、Richard J. Pariza、Steven R. Crowley、Andre G. Pernet、Paul R. Bunnell、Patrick W. Dodge
    DOI:10.1021/jm00374a014
    日期:1984.8
    A series of substituted 5,6-dihydrofuro[3,2-f]-1,2-benzisoxazoles was prepared and evaluated for their saluretic and uricosuric properties. Pharmacological evaluation of the title compounds was carried out in mice, rats, dogs, and monkeys. The diuretic/saluretic nature of these compounds was observed in all species, whereas the uricosuric activity was best seen in the Cebus monkey. Evaluation of the enantiomers of 8-chloro-3-(o-fluorophenyl)-5,6-dihydrofuro [3,2-f]-1,2-benzisoxazole-6-carboxylic acid (15k) revealed that only the (+) enantiomer (29) displayed diuretic and saluretic activity, whereas both enantiomers possessed uricosuric activity. X-ray analysis showed that the (-) enantiomer (30) possesses the 2R configuration.
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