(1-allyl-4,5,6,7-tetrahydro-1H-benzimidazole-2-yl)[4-methylphenyl]methanone | 840503-10-8

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: (1-allyl-4,5,6,7-tetrahydro-1H-benzimidazole-2-yl)[4-methylphenyl]methanone
• 英文别名: (1-allyl-4,5,6,7-tetrahydro-1H-benzimidazol-2-yl)(4-methylphenyl)methanone；(4-Methylphenyl)-(1-prop-2-enyl-4,5,6,7-tetrahydrobenzimidazol-2-yl)methanone
• CAS: 840503-10-8
• 化学式: C₁₈H₂₀N₂O
• 分子量: 280.37
• InChiKey: TWIAZAHWTLLVMQ-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.9
• 重原子数：
  21
• 可旋转键数：
  4
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.33
• 拓扑面积：
  34.9
• 氢给体数：
  0
• 氢受体数：
  2

反应信息

• 作为反应物：
  描述：

  (1-allyl-4,5,6,7-tetrahydro-1H-benzimidazole-2-yl)[4-methylphenyl]methanone 、 tert-butyl 2-(3-iodophenoxy)-2-methylpropanoate 在 N-甲基二环己基胺 、 苄基三乙基氯化铵 、 palladium diacetate 作用下， 以 N,N-二甲基甲酰胺 为溶剂， 生成
  参考文献：
  名称：

  Synthesis and pharmacological evaluation of novel benzoylazole-based PPAR α/γ activators

  摘要：

  In our search for new PPAR alpha/gamma agonists, we designed and synthesized a series of benzoylazole-based carboxylic acids. Compound 9 showed potent PPAR gamma partial agonistic activity with modest PPAR alpha agonistic activity. The sodium salt of 9 (9Na) demonstrated potent efficacy in lowering both blood glucose and lipids in an animal model without causing significant body weight gain, a well-known side effect associated with PPAR gamma full agonists. (C) 2011 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2011.02.032
• 作为产物：
  描述：

  4,5,6,7-四氢-1H-苯并咪唑 在 18-冠醚-6 、 potassium carbonate 、 三乙胺 作用下， 以 四氢呋喃 、 吡啶 为溶剂， 生成 (1-allyl-4,5,6,7-tetrahydro-1H-benzimidazole-2-yl)[4-methylphenyl]methanone
  参考文献：
  名称：

  Synthesis and pharmacological evaluation of novel benzoylazole-based PPAR α/γ activators

  摘要：

  In our search for new PPAR alpha/gamma agonists, we designed and synthesized a series of benzoylazole-based carboxylic acids. Compound 9 showed potent PPAR gamma partial agonistic activity with modest PPAR alpha agonistic activity. The sodium salt of 9 (9Na) demonstrated potent efficacy in lowering both blood glucose and lipids in an animal model without causing significant body weight gain, a well-known side effect associated with PPAR gamma full agonists. (C) 2011 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2011.02.032

文献信息

• Novel Heteroaryl Derivative
  申请人：Takahashi Yoko

  公开号：US20080167306A1

  公开（公告）日：2008-07-10

  A compound of the following formula (1), or its prodrug or pharmaceutically acceptable salt thereof, being useful as a diabetic medicine or preventive, or blood sugar regulator, or therapeutic agent for hyperlipemia, etc. wherein the ring Z is an optionally substituted heteroaryl, W 4 is a single bond, lower alkylene, etc., Ar 2 is an optionally substituted aryl, etc., W 3 is a single bond, lower alkylene, etc., Ar 1 is an optionally substituted arylene, etc., each of W 1 and W 2 is an optionally substituted lower alkylene, etc., and R 1 is carboxyl, an alkoxycarbonyl.

  下列式子（1）的化合物，或其前药或其药学上可接受的盐，被用作糖尿病药物或预防药物，或血糖调节剂，或高脂血症等治疗剂。其中，环Z是可选取代的杂芳基，W4是单键，低碳链等，Ar2是可选取代的芳基等，W3是单键，低碳链等，Ar1是可选取代的芳烃基等，W1和W2是可选取代的低碳链等，R1是羧基，烷氧羰基等。
• HETEROARYL DERIVATIVES
  申请人：TAKAHASHI Yoko

  公开号：US20100286144A1

  公开（公告）日：2010-11-11

  A compound of the following formula (1), or its prodrug or pharmaceutically acceptable salt thereof, being useful as a diabetic medicine or preventive, or blood sugar regulator, or therapeutic agent for hyperlipemia, etc. wherein the ring Z is an optionally substituted heteroaryl, W 4 is a single bond, lower alkylene, etc., Ar 2 is an optionally substituted aryl, etc., W 3 is a single bond, lower alkylene, etc., Ar 1 is an optionally substituted arylene, etc., each of W 1 and W 2 is an optionally substituted lower alkylene, etc., and R 1 is carboxyl, an alkoxycarbonyl.

  以下式子（1）的化合物，或其前药或药学上可接受的盐，可用作糖尿病药物、预防药物、血糖调节剂或高脂血症等治疗剂。 其中，环Z是可选取的取代杂环基，W4是单键，低碳烷基等，Ar2是可选取的取代芳基等，W3是单键，低碳烷基等，Ar1是可选取的取代芳烃基等，W1和W2各自是可选取的取代低碳烷基等，R1是羧基，烷氧羰基等。
• NOVEL HETEROARYL DERIVATIVE
  申请人：Dainippon Sumitomo Pharma Co., Ltd.

  公开号：EP1647546B1

  公开（公告）日：2012-05-02
• US7425642B2
  申请人：——

  公开号：US7425642B2

  公开（公告）日：2008-09-16
• US7781479B2
  申请人：——

  公开号：US7781479B2

  公开（公告）日：2010-08-24