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(2-甲氧基苯基)氨基磺酸酯 | 57651-00-0

中文名称
(2-甲氧基苯基)氨基磺酸酯
中文别名
——
英文名称
Sulfamidsaeure-o-methoxyphenylester
英文别名
Sulfamic acid 2-methoxyphenyl ester;2-Methoxyphenyl sulfamate;(2-methoxyphenyl) sulfamate
(2-甲氧基苯基)氨基磺酸酯化学式
CAS
57651-00-0
化学式
C7H9NO4S
mdl
——
分子量
203.219
InChiKey
SJQLKTNUZIPAPJ-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):
    0.5
  • 重原子数:
    13
  • 可旋转键数:
    3
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.14
  • 拓扑面积:
    87
  • 氢给体数:
    1
  • 氢受体数:
    5

SDS

SDS:36497d705ce6b34caf310d613038036f
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反应信息

  • 作为产物:
    参考文献:
    名称:
    Aryl and aryloxyalkyl sulfamate esters useful as anticonvulsants
    摘要:
    以下披露了一种使用含有化合物的药物组合物来治疗惊厥的方法:(HO).sub.p --A--[OSO.sub.2 NR.sup.1 R.sup.2 ].sub.z,其中A是芳基、芳基烷基或芳氧烷基基团,并在1个或多个碳原子上用磺酰胺基团(--OSO.sub.2 NR.sup.1 R.sup.2)取代,其中R.sup.1和R.sup.2,相同或不同,是氢或较低烷基,其中p为0或1,是未处理的羟基团的数量,z为1或2,是--OS(O.sub.2)NR.sup.1 R.sup.2基团的数量。芳基选自苯基、取代苯基、吡啶基、萘基、喹啉基等。苯基取代基选自氢、卤素、羟基、苯基、苯氧基、苯甲酰基、较低烷基、较低烷氧基、羧基、氨基、较低烷基氨基、二较低烷基氨基、乙酰胺基、氰基、硝基、较低烷氧羰基、氨基磺酰基、咪唑基、三唑基等。还描述了以前未披露的新化合物。
    公开号:
    US05025031A1
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文献信息

  • Sulfamates as antiglaucoma agents
    申请人:A. H. Robins Company, Incorporated
    公开号:US05192785A1
    公开(公告)日:1993-03-09
    Sulfamate esters of the formula (HO).sub.p --A--[OSO.sub.2 NR.sup.1 R.sup.2 ].sub.z where A is aryloxyalkyl, p is the number of unreacted hydroxy groups present on the alkyl moiety and may be zero, z is the number of --OS(O).sub.2 NR.sup.1 R.sup.2 groups attached to carbons of the alkyl moiety and is always at least one; R.sup.1 and R.sup.2 are selected from hydrogen, loweralkyl, carboxy, and the like are useful in treating glaucoma.
    Sulfamate酯的化学式为(HO).sub.p --A--[OSO.sub.2 NR.sup.1 R.sup.2 ].sub.z,其中A为芳基氧烷基,p为烷基部分上存在的未反应羟基的数量,可以为零,z为连接到烷基部分碳上的--OS(O).sub.2 NR.sup.1 R.sup.2基团的数量,始终至少为一;R.sup.1和R.sup.2从氢、低烷基、羧基等中选择,在治疗青光眼方面是有用的。
  • Compounds having one or more aminosulfaonyloxy radicals useful as
    申请人:A. H. Robins Company, Incorporated
    公开号:US05194446A1
    公开(公告)日:1993-03-16
    Methods of treating chronic arthritis and osteoporosis which utilize both known and novel compounds which would fall under the general formula: (HO)p--A--[--OS(O).sub.2 NR.sup.1 R.sup.2 ].sub.z wherein A encompasses a wide range of values including but not limited to aryl, loweralkyl, cycloalkyl, and carbohydrates including sucrose and fructose; p is equal to the number of unreacted hydroxy groups contained on the molecule and may be zero; z is the number of --OS(O).sub.2 NR.sup.1 R.sup.2 groups and is always at least one; R.sup.1 and R.sup.2 are selected from hydrogen, loweralkyl, carboxy and the like; a novel process for preparing the compounds is provided wherein an appropriate sulfamic acid aryl ester is reacted with a hydroxy substituted A radical which may or may not contain thereon protected carboxyl, amino or hydroxy substituents, in an aprotic solvent containing a tertiary amine base. Pharmaceutical compositions for the treatment of chronic arthritis and osteoporosis are also provided.
    治疗慢性关节炎和骨质疏松症的方法利用已知和新颖的化合物,这些化合物可归入一般公式:(HO)p--A--[--OS(O).sub.2 NR.sup.1 R.sup.2 ].sub.z,其中A包括一系列值,包括但不限于芳基、较低烷基、环烷基和碳水化合物,包括蔗糖和果糖;p等于分子中未反应的羟基数,可以为零;z是--OS(O).sub.2 NR.sup.1 R.sup.2基团的数量,始终至少为一;R.sup.1和R.sup.2从氢、较低烷基、羧基等中选择;提供了一种制备这些化合物的新方法,其中适当的磺酸酯与含有保护羧基、氨基或羟基取代基的羟基取代的A基团在含有三级胺碱的无水溶剂中反应。还提供了用于治疗慢性关节炎和骨质疏松症的药物组合物。
  • Compounds having one or more aminosulfonyloxy radicals useful as pharmaceuticals
    申请人:A.H. ROBINS COMPANY, INCORPORATED
    公开号:EP0403185A2
    公开(公告)日:1990-12-19
    The invention concerns known and novel compounds which fall under the general formula: wherein A encompasses a wide range of values including but not limited to aryl, loweralkyl, cycloalkyl, and carbohydrates including sucrose and fructose; p is equal to the number of hydroxy groups on A and may be zero; z is the number of -OS(O)2NR1R2 groups and is always at least one; R1 and R2 are selected from hydrogen, loweralkyl, carboxy and the like; which compounds are useful for treating chronic arthritis and osteoporosis. A novel process for preparing the compounds is provided wherein an appropriate sulfamic acid aryl ester is reacted with a a hydroxy substituted A radical which may or may not contain thereon protected carboxyl, amino or hydroxy substituents, in an aprotic solvent containing a tertiary amine base. Pharmaceutical compositions for the treatment of chronic arthritis and osteoporosis are also provided.
    本发明涉及属于通式的已知和新型化合物: 其中,A 的数值范围很广,包括但不限于芳基、低级烷基、环烷基以及包括蔗糖和果糖在内的碳水化合物;p 等于 A 上羟基的数目,可以是零;z 是 -OS(O)2NR1R2 基团的数目,总是至少一个;R1 和 R2 选自氢、低级烷基、羧基等;这些化合物可用于治疗慢性关节炎和骨质疏松症。本发明提供了一种制备这些化合物的新工艺,即在含有叔胺基的钝溶剂中,将适当的氨基磺酸芳基酯与羟基取代的 A 基反应,A 基上可以含有或不含有受保护的羧基、氨基或羟基取代基。此外,还提供了用于治疗慢性关节炎和骨质疏松症的药物组合物。
  • DIARYL- -LACTAM COMPOUND AND PREPARATION METHOD AND PHARMACEUTICAL USE THEREOF
    申请人:Fudan University
    公开号:EP3438105B1
    公开(公告)日:2022-01-05
  • US5025031A
    申请人:——
    公开号:US5025031A
    公开(公告)日:1991-06-18
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