5-(3-(2,6-dimethylbenzyloxy)benzyl)-1H-tetrazole | 1193434-40-0

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯酚醚
• 英文名称: 5-(3-(2,6-dimethylbenzyloxy)benzyl)-1H-tetrazole
• 英文别名: 5-[[3-[(2,6-dimethylphenyl)methoxy]phenyl]methyl]-2H-tetrazole
• CAS: 1193434-40-0
• 化学式: C₁₇H₁₈N₄O
• 分子量: 294.356
• InChiKey: KJVQFGWUVANOSW-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.6
• 重原子数：
  22
• 可旋转键数：
  5
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.24
• 拓扑面积：
  63.7
• 氢给体数：
  1
• 氢受体数：
  4

反应信息

• 作为产物：
  描述：

  3-羟基苯乙腈 在 sodium azide 、 偶氮二甲酸二异丙酯 、 氯化铵 、 三苯基膦 作用下， 以 四氢呋喃 、 N,N-二甲基甲酰胺 为溶剂， 反应 25.0h， 生成 5-(3-(2,6-dimethylbenzyloxy)benzyl)-1H-tetrazole
  参考文献：
  名称：

  TETRAZOLE COMPOUNDS FOR REDUCING URIC ACID

  摘要：

  公开号：

  EP2282736B1

文献信息

• Tetrazole compounds for reducing uric acid
  申请人：Wellstat Therapeutics Corporation

  公开号：US08889724B2

  公开（公告）日：2014-11-18

  Uric acid in mammalian subjects is reduced and excretion of uric acid is increased by administering a compound of Formula I. The uric acid-lowering effects of the compounds of this invention are used to treat or prevent a variety of conditions including gout, hyperuricemia, elevated levels of uric acid that do not meet the levels customarily justifying a diagnosis of hyperuricemia, renal dysfunction, kidney stones, cardiovascular disease, risk for developing cardiovascular disease, tumor-lysis syndrome, cognitive impairment, early-onset essential hypertension, and Plasmodium falciparum-induced inflammation.

  在哺乳动物中，通过给予公式I的化合物，可以降低尿酸并增加尿酸的排泄。这种发明的化合物的降低尿酸作用可用于治疗或预防多种疾病，包括痛风、高尿酸血症、尿酸水平升高但不符合通常诊断为高尿酸血症的水平、肾功能障碍、肾结石、心血管疾病、发生心血管疾病的风险、肿瘤溶解综合征、认知障碍、早发性高血压和疟原虫引起的炎症。
• US8410154B2
  申请人：——

  公开号：US8410154B2

  公开（公告）日：2013-04-02
• US8889724B2
  申请人：——

  公开号：US8889724B2

  公开（公告）日：2014-11-18
• [EN] TETRAZOLE COMPOUNDS FOR REDUCING URIC ACID<br/>[FR] COMPOSÉS DE TÉTRAZOLE POUR RÉDUIRE L'ACIDE URIQUE
  申请人：WELLSTAT THERAPEUTICS CORP

  公开号：WO2009134995A2

  公开（公告）日：2009-11-05

  Uric acid in mammalian subjects is reduced and excretion of uric acid is increased by administering a compound of Formula I. The uric acid-lowering effects of the compounds of this invention are used to treat or prevent a variety of conditions including gout, hyperuricemia, elevated levels of uric acid that do not meet the levels customarily justifying a diagnosis of hyperuricemia, renal dysfunction, kidney stones, cardiovascular disease, risk for developing cardiovascular disease, tumor-lysis syndrome, cognitive impairment, early-onset essential hypertension, and Plasmodiumfalciparum-induced inflammation. In Formula 1, x is 1 or 2: y is O, 1, 2 or 3; and R1 is selected from the group consisting of hydrogen, alkyl having 1 or 2 carbon atoms, hydroxy, alkoxy having 1 or 2 carbon atoms, fluoro. chloro, bromo, and amino. A is phenyl unsubstituted or substituted by one, two or three groups selected from the group consisting of halo, alkyl having 1 or 2 carbon atoms. perfluoromethyL alkoxy having 1 or 2 carbon atoms, and perfluoromethoxy; or cycloalkyl having from 3 to 6 ring atoms wherein the cycloalky! is unsubstituted or one one two ring carbons are independently mono-substituted by methyl or ethyl; or a 5 or 6 membered heleraromatic ring having 1 or 2 ring heteroatoms selected from N. S and O and the heteroaromatic ring is covalently bound to the remainder of the compound by a ring carbon.