2-[2-(4-chloro-phenyl)-5-methyl-oxazol-4-yl]-ethanol | 475481-50-6

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 唑类
• 英文名称: 2-[2-(4-chloro-phenyl)-5-methyl-oxazol-4-yl]-ethanol
• 英文别名: 2-(4-chlorophenyl)-5-methyl-oxazole ethanol；2-[2-(4-chlorophenyl)-5-methyl-1,3-oxazol-4-yl]ethanol
• CAS: 475481-50-6
• 化学式: C₁₂H₁₂ClNO₂
• 分子量: 237.686
• InChiKey: NDBNMDJZTBKWJG-UHFFFAOYSA-N

物化性质

• 沸点：
  389.5±52.0 °C(Predicted)
• 密度：
  1?+-.0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  2.6
• 重原子数：
  16
• 可旋转键数：
  3
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.25
• 拓扑面积：
  46.3
• 氢给体数：
  1
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  2-[2-(4-chloro-phenyl)-5-methyl-oxazol-4-yl]-ethanol 在 lithium hydroxide 、 三苯基膦 、 1,1'-azodicarbonyl-dipiperidine 作用下， 以 四氢呋喃 、 甲醇 为溶剂， 生成 2-(5-{2-[2-(4-chlorophenyl)-5-methyl-1,3-oxazol-4-yl]ethoxy}-2,3-dihydro-1H-inden-1-yl)butanoic acid
  参考文献：
  名称：

  Substituted indanylacetic acids as PPAR-α–γ activators

  摘要：

  A series of oxazole-substituted indanylacetic acids were prepared which show a spectrum of activity as ligands for PPAR nuclear receptor subtypes. (c) 2005 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2005.10.008

文献信息

• Oxazole derivatives
  申请人：——

  公开号：US20030055265A1

  公开（公告）日：2003-03-20

  The present invention relates to novel oxazole compounds which act as PPAR&agr; and PPAR&ggr; agonists and are accordingly useful for the treatment of diseases modulated by PPAR&agr; and PPAR&ggr; such as diabetes.

  本发明涉及新型噁唑化合物，其作为PPAR&agr;和PPAR&ggr;激动剂，并因此可用于治疗由PPAR&agr;和PPAR&ggr;调节的疾病，如糖尿病。
• DPP IV inhibitors
  申请人：——

  公开号：US20030130281A1

  公开（公告）日：2003-07-10

  The present invention relates to compounds of formula (I) 1 wherein R 1 , R 2 , and X are as defined in the description and claims, and pharmaceutically acceptable salts thereof. The compounds are useful for the treatment and/or prophylaxis of diseases which are associated with DPP IV, such as diabetes, particularly non-insulin dependent diabetes mellitus, and impaired glucose tolerance.

  本发明涉及以下式（I）的化合物： 其中R1、R2和X如描述和权利要求中所定义，并且其药学上可接受的盐。这些化合物可用于治疗和/或预防与DPP IV相关的疾病，如糖尿病，特别是非胰岛素依赖型糖尿病和糖耐量受损。
• [EN] CHIRALE OXAZOLE-ARYLPROPIONIC ACID DERIVATIVES AND THEIR USE AS PPAR AGONISTS<br/>[FR] DERIVES D'ACIDE OXAZOLE-ARYLPROPIONIQUE CHIRAL ET LEUR UTILISATION EN TANT QU'AGONISTES DU RECEPTEUR PPAR
  申请人：HOFFMANN LA ROCHE

  公开号：WO2004031162A1

  公开（公告）日：2004-04-15

  The present invention relates to compounds of Formula (I), wherein R1 to R6 and n are as defined in the description and claims, and pharmaceutically acceptable salts and esters thereof. The compounds are useful for the treatment and/or prevention of diseases, which are modulated by PPARα and/or PPARϜ agonists as e.g. type II diabetes.

  本发明涉及式（I）的化合物，其中R1至R6和n如描述和索赔中所定义，并且其药学上可接受的盐和酯。这些化合物可用于治疗和/或预防由PPARα和/或PPARϜ激动剂调节的疾病，例如II型糖尿病。
• Studies on antidiabetic agents. 11. Novel thiazolidinedione derivatives as potent hypoglycemic and hypolipidemic agents
  作者：Takashi Sohda、Katsutoshi Mizuno、Yu Momose、Hitoshi Ikeda、Takeshi Fujita、Kanji Meguro

  DOI：10.1021/jm00092a012

  日期：1992.7

  antidiabetic pioglitazone (AD-4833, U-72,107), a series of 5-[4-(2- or 4-azolylalkoxy)benzyl- or -benzylidene]-2,4-thiazolidinediones was prepared and evaluated for hypoglycemic and hypolipidemic activities in insulin-resistant, genetically obese, and diabetic KKA(y) mice. Replacement of the 2-pyridyl moiety of pioglitazone by a 2- or 4-oxazolyl or a 2- or 4-thiazolyl moiety greatly enhanced in vivo potency

  在新型抗糖尿病吡格列酮的进一步化学修饰过程中（AD-4833，U-72,107），一系列5- [4-（2-或4-偶氮烷氧基）苄基或亚苄基] -2,4-噻唑烷二酮制备并评估了胰岛素抵抗，遗传性肥胖和糖尿病KKA（y）小鼠的降血糖和降血脂活性。吡格列酮的2-吡啶基部分被2-或4-恶唑基或2-或4-噻唑基部分取代大大增强了体内效力。相应的5-亚苄基型化合物也具有有效的生物活性，其中次甲基用作苯环和噻唑烷二酮环之间的连接基。在合成的化合物中，5- [4- [2-（5-甲基-2-苯基-4-恶唑基）乙氧基]苄基] -2,4-噻唑烷二酮（18）表现出最强的活性，是其的100倍以上吡格列酮。
• [EN] OXAZOLE DERIVATIVES AS HISTAMINE H3 RECEPTOR AGENTS, PREPARATION AND THERAPEUTIC USES<br/>[FR] DERIVES D'OXAZOLE EN TANT QU'AGENTS DE RECEPTEUR D'HISTAMINE H3, PREPARATION ET UTILISATIONS THERAPEUTIQUES
  申请人：LILLY CO ELI

  公开号：WO2006019833A1

  公开（公告）日：2006-02-23

  The present invention discloses novel aryl oxazole compounds of Formula I (I), or pharmaceutically acceptable salts thereof, which have histamine-H3 receptor antagonist or inverse agonist activity, as well as methods for preparing and using such compounds. In another embodiment, the invention discloses pharmaceutical compositions comprising compounds of Formula I as well as methods of using these compositions to treat obesity, cognitive deficiencies, narcolepsy, and other histamine H3 receptor-related diseases. Formula I (I) or a pharmaceutically acceptable salt thereof, wherein: m is independenlly at each occurrence 1, 2, or 3, Z independently represents carbon (substituted with hydrogen or the optional substituents indicated herein) or nitrogen, provided that when Z is nitrogen then R6 is not attached to Z; R1 and R2 are independently -(C1-C7) alkyl(optionally substituted with one to three halogens), or R1 and R2 and the nitrogen to which they are attached form an azetidinyl ring, a pyrrolidinyl ring, or a piperidinyl ring, wherein further the azetidinyl, pyrrolidinyl, or piperidinyl ring so formed may be optionally substituted one to three times with R5; R6 is independently at each occurrence -H, -halogen, or -CH3.

  本发明公开了具有组分I（I）的新型芳基噁唑化合物或其药学上可接受的盐，其具有组胺H3受体拮抗剂或逆向激动剂活性，以及制备和使用这些化合物的方法。在另一实施方案中，本发明公开了包括组分I化合物的药物组合物，以及使用这些组合物治疗肥胖、认知缺陷、嗜睡症和其他组胺H3受体相关疾病的方法。组分I（I）或其药学上可接受的盐，其中：m在每次出现时独立地为1、2或3，Z独立地表示碳（用氢或此处指示的可选取代基团取代）或氮，但当Z为氮时，R6不连接到Z；R1和R2独立地为-(C1-C7)烷基（可选地用一到三个卤素取代），或者R1和R2以及它们连接的氮形成氮杂环戊二烷环、吡咯环或哌啶环，进一步地，所形成的氮杂环戊二烷、吡咯环或哌啶环可以用R5取代一到三次；R6在每次出现时独立地为-H、-卤素或-CH3。