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3,5-dichloro-N-[6-(5-methyl-[1,2,4]oxadiazol-3-yl)-naphthalen-1-yl]-phenylsulphonamide | 1131395-12-4

中文名称
——
中文别名
——
英文名称
3,5-dichloro-N-[6-(5-methyl-[1,2,4]oxadiazol-3-yl)-naphthalen-1-yl]-phenylsulphonamide
英文别名
3,5-dichloro-N-[6-(5-methyl-1,2,4-oxadiazol-3-yl)naphthalen-1-yl]benzenesulfonamide
3,5-dichloro-N-[6-(5-methyl-[1,2,4]oxadiazol-3-yl)-naphthalen-1-yl]-phenylsulphonamide化学式
CAS
1131395-12-4
化学式
C19H13Cl2N3O3S
mdl
——
分子量
434.303
InChiKey
QQQRBSZPZRIEPG-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):
    5.2
  • 重原子数:
    28
  • 可旋转键数:
    4
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.05
  • 拓扑面积:
    93.5
  • 氢给体数:
    1
  • 氢受体数:
    6

反应信息

  • 作为产物:
    描述:
    6-(5-methyl-[1,2,4]oxadiazol-3-yl)-naphthalene-1-boronic acid3,5-二氯苯磺酰胺 在 copper diacetate 三乙胺 作用下, 以 二氯甲烷 为溶剂, 反应 24.0h, 以31%的产率得到3,5-dichloro-N-[6-(5-methyl-[1,2,4]oxadiazol-3-yl)-naphthalen-1-yl]-phenylsulphonamide
    参考文献:
    名称:
    [EN] NEW ARYLSULPHONYLGLYCINE DERIVATIVES, THE PREPARATION THEREOF AND THEIR USE AS MEDICAMENTS
    [FR] NOUVEAUX DÉRIVÉS D'ARYLSULFONYLGLYCINE, LEUR FABRICATION ET LEUR UTILISATION EN TANT QUE MÉDICAMENTS
    摘要:
    这项发明涉及通式(I)中取代芳基磺酰甘氨酸衍生物,其中基团Ra至Rf、A和Z的定义如规范和索赔中所述,适用于制备用于治疗代谢紊乱,特别是1型或2型糖尿病的药物组合物。
    公开号:
    WO2009127723A1
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文献信息

  • [EN] ARYLSULFONYLAMINOMETHYLPHOSPHONIC ACID DERIVATIVES, THE PREPARATION THEREOF AND THE USE THEREOF AS PHARMACEUTICAL COMPOSITIONS<br/>[FR] DÉRIVÉS D'ACIDE ARYLSULFONYLAMINOMÉTHYLPHOSPHONIQUE, PRÉPARATION DE CEUX-CI ET UTILISATION DE CEUX-CI COMME COMPOSITIONS PHARMACEUTIQUES
    申请人:BOEHRINGER INGELHEIM INT
    公开号:WO2009030715A1
    公开(公告)日:2009-03-12
    The invention relates tosubstitutedarylsulphonylaminomethylphosphonic acid derivativesof general formula (I) wherein the groups Ra to Rf, A and Z are defined as mentioned in the specification and claims, which are suitable for preparinga medicament for the treatmentof metabolic disorders, particularlytype 1 or type 2 diabetesmellitus.
    该发明涉及通式(I)的取代芳基磺胺甲基膦酸衍生物,其中基团Ra至Rf、A和Z的定义如规范和权利要求中所述,适用于制备用于治疗代谢紊乱,特别是1型或2型糖尿病的药物。
  • ARYLSULPHONYLGLYCINE DERIVATIVES, THE PREPARATION THEREOF AND THEIR USE AS MEDICAMENTS
    申请人:Langkopf Elke
    公开号:US20110269761A1
    公开(公告)日:2011-11-03
    The invention relates to substituted aryl-sulphonylglycine derivatives of general formula (I) wherein the groups R a to R f , A and Z are defined as in the specification and claims, which are suitable for preparing a pharmaceutical composition for the treatment of metabolic disorders, particularly type 1 or type 2 diabetes mellitus.
    本发明涉及一种通式(I)的取代芳基磺酰基甘氨酸衍生物,其中基团R至Rf、A和Z的定义如规范和要求中所述,适用于制备治疗代谢性疾病,特别是1型或2型糖尿病的药物组合物。
  • ARYLSULFONYLAMINOMETHYLPHOSPHONIC ACID DERIVATIVES, THE PREPARATION THEREOF AND THE USE THEREOF AS PHARMACEUTICAL COMPOSITIONS
    申请人:Langkopf Elke
    公开号:US20100261677A1
    公开(公告)日:2010-10-14
    The invention relates to substituted arylsulphonylaminomethylphosphonic acid derivatives of general formula (I) wherein the groups R a to R f , A and Z are defined as mentioned in the specification and claims, which are suitable for preparing a medicament for the treatment of metabolic disorders, particularly type 1 or type 2 diabetes mellitus.
    本发明涉及一种通式(I)的取代芳基磺酰氨甲基膦酸衍生物,其中R到Rf,A和Z的基团如说明书和权利要求中所述,适用于制备用于治疗代谢性疾病,特别是1型或2型糖尿病的药物。
  • US8163911B2
    申请人:——
    公开号:US8163911B2
    公开(公告)日:2012-04-24
  • [EN] NEW ARYLSULPHONYLGLYCINE DERIVATIVES, THE PREPARATION THEREOF AND THEIR USE AS MEDICAMENTS<br/>[FR] NOUVEAUX DÉRIVÉS D'ARYLSULFONYLGLYCINE, LEUR FABRICATION ET LEUR UTILISATION EN TANT QUE MÉDICAMENTS
    申请人:BOEHRINGER INGELHEIM INT
    公开号:WO2009127723A1
    公开(公告)日:2009-10-22
    The invention relates to substituted arylsulphonylglycine derivatives of general formula (I) wherein the groups Ra to Rf, A and Z are defined as in the specification and claims, which are suitable for preparing a pharmaceutical composition for the treatment of metabolic disorders, particularly type 1 or type 2 diabetes mellitus.
    这项发明涉及通式(I)中取代芳基磺酰甘氨酸衍生物,其中基团Ra至Rf、A和Z的定义如规范和索赔中所述,适用于制备用于治疗代谢紊乱,特别是1型或2型糖尿病的药物组合物。
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