N-(piperidin-3-ylmethyl)-2-(4-chlorophenyl)-4-methylthiazole-5-carboxamide | 876147-54-5

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 唑类
• 英文名称: N-(piperidin-3-ylmethyl)-2-(4-chlorophenyl)-4-methylthiazole-5-carboxamide
• 英文别名: N-(Piperidin-3-yl methyl)-2-(4-chlorophenyl)-4-methylthiazole-5-carboxamide；2-(4-chlorophenyl)-4-methyl-N-(piperidin-3-ylmethyl)-1,3-thiazole-5-carboxamide
• CAS: 876147-54-5
• 化学式: C₁₇H₂₀ClN₃OS
• 分子量: 349.884
• InChiKey: FGJNDTVPYFCIPX-UHFFFAOYSA-N

物化性质

• 密度：
  1.229±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  3.6
• 重原子数：
  23
• 可旋转键数：
  4
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.41
• 拓扑面积：
  82.3
• 氢给体数：
  2
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  N-(piperidin-3-ylmethyl)-2-(4-chlorophenyl)-4-methylthiazole-5-carboxamide 在 四丁基碘化铵 盐酸 、 氢氧化钾 、 水 、 苄基三甲基氢氧化铵 、 potassium carbonate 作用下， 以 四氢呋喃 、 甲醇 、 N,N-二甲基甲酰胺 为溶剂， 反应 14.0h， 生成 2-[3-[[2-(4-chlorophenyl)-4-methylthiazol-5-yl]carbonylaminomethyl]piperidin-1-yl]phenylacetic acid
  参考文献：
  名称：

  EP1862464

  摘要：

  公开号：
• 作为产物：
  描述：

  2-(4-氯苯基)-4-甲基-1,3-噻唑-5-羧酸 在 N-甲基吗啉 、 盐酸 、 1-羟基苯并三唑 、 盐酸-N-乙基-Nˊ-(3-二甲氨基丙基)碳二亚胺 作用下， 以 甲醇 、 N,N-二甲基甲酰胺 为溶剂， 反应 7.17h， 生成 N-(piperidin-3-ylmethyl)-2-(4-chlorophenyl)-4-methylthiazole-5-carboxamide
  参考文献：
  名称：

  EP1862464

  摘要：

  公开号：

文献信息

• Novel Cyclic Amino Benzoic Acid Derivative
  申请人：Nomura Masahiro

  公开号：US20070249580A1

  公开（公告）日：2007-10-25

  The present invention relates to cyclic amino benzoic acid derivatives which are effective in therapy of lipid metabolism abnormality, diabetes and the like as a human peroxisome proliferators-activated receptor (PPAR) agonist, in particular, as an agonist against human PPARα isoform, and addition salts thereof, and pharmaceutical compositions containing these compounds. A cyclic amino benzoic acid derivative represented by the general formula (1) [wherein a ring Ar represents an aryl group which may have substituent, or the like; Y represents a C 1 -C 4 alkylene, C 2 -C 4 alkenylene, C 2 -C 4 alkynylene, or the like; Z represents an oxygen atom, sulfur atom or —(CH 2 ) n — (n represents 0, 1 or 2); X represents a hydrogen atom, halogen atom, lower alkyl group which may be substituted with a halogen atom, or the like; R represents a hydrogen atom or lower alkyl group, and —COOR substitutes for an ortho position or metha position of binding position of ring W] or a pharmaceutically acceptable salt thereof.

  本发明涉及循环氨基苯甲酸衍生物，作为人类过氧化物酶体增殖物激活受体（PPAR）激动剂，在治疗脂质代谢异常、糖尿病等方面具有有效性，特别是作为人类PPARα亚型的激动剂，以及其加成盐和含有这些化合物的药物组合物。其中，循环氨基苯甲酸衍生物的一般式（1）表示为[其中，环Ar表示可能具有取代基的芳基；Y表示C1-C4烷基、C2-C4烯基、C2-C4炔基或类似物；Z表示氧原子、硫原子或—（CH2）n—（n表示0、1或2）；X表示氢原子、卤原子、可能带有卤原子取代的低烷基或类似物；R表示氢原子或低烷基，而—COOR代替环W的结合位置的邻位或间位]或其药学上可接受的盐。
• Novel Cyclic Aminophenylalkanoic Acid Derivative
  申请人：Nomura Masahiro

  公开号：US20090036489A1

  公开（公告）日：2009-02-05

  The present invention provides cyclic aminophenylalkanoic acid derivatives that act as agonists for human peroxisome proliferator-activated receptors (PPARs), in particular human PPARα isoform, and are effective in the treatment of abnormal lipid metabolism, diabetes and other disorders. The present invention also provides addition salts of such cyclic aminophenylalkanoic acid derivatives and pharmaceutical compositions containing these compounds. Specifically, the present invention provides cyclic aminophenylalkanoic acid derivatives represented by the following general formula (1): , or pharmaceutically acceptable salts thereof.

  本发明提供了环状氨基苯基脂肪酸衍生物，其作为人类过氧化物酶体增殖物激活受体（PPARs）的激动剂，尤其是人类PPARα亚型，并且对于治疗异常脂质代谢、糖尿病和其他疾病具有疗效。本发明还提供这些环状氨基苯基脂肪酸衍生物的加成盐和含有这些化合物的制药组合物。具体而言，本发明提供由以下通式（1）表示的环状氨基苯基脂肪酸衍生物，或其药学上可接受的盐。
• Cyclic amino benzoic acid derivative
  申请人：Kyorin Pharmaceutical Co., Ltd.

  公开号：US07902367B2

  公开（公告）日：2011-03-08

  The present invention relates to cyclic amino benzoic acid derivatives which are effective in therapy of lipid metabolism abnormality, diabetes and the like as a human peroxisome proliferators-activated receptor (PPAR) agonist, in particular, as an agonist against human PPARα isoform, and addition salts thereof, and pharmaceutical compositions containing these compounds. A cyclic amino benzoic acid derivative represented by the general formula (1) [wherein a ring Ar represents an aryl group which may have substituent, or the like; Y represents a C1-C4 alkylene, C2-C4 alkenylene, C2-C4 alkynylene, or the like; Z represents an oxygen atom, sulfur atom or —(CH2)n— (n represents 0, 1 or 2); X represents a hydrogen atom, halogen atom, lower alkyl group which may be substituted with a halogen atom, or the like; R represents a hydrogen atom or lower alkyl group, and —COOR substitutes for an ortho position or metha position of binding position of ring W] or a pharmaceutically acceptable salt thereof.

  本发明涉及循环氨基苯甲酸衍生物，其作为人类过氧化物酶体增殖物激活受体（PPAR）激动剂在治疗脂质代谢异常、糖尿病等方面具有有效性，特别是作为人类PPARα亚型的激动剂，以及其加成盐和含有这些化合物的制药组合物。其中循环氨基苯甲酸衍生物的一般式（1）表示为[其中环Ar表示可能具有取代基的芳基基团或类似物；Y表示C1-C4烷基，C2-C4烯基，C2-C4炔基或类似物；Z表示氧原子、硫原子或—（CH2）n—（n表示0、1或2）；X表示氢原子、卤原子、可能被卤原子取代的低烷基基团或类似物；R表示氢原子或低烷基基团，而—COOR代替环W的连接位置的邻位或甲位]或其药学上可接受的盐。
• NOVEL CYCLIC AMINOBENZOIC ACID DERIVATIVE
  申请人：KYORIN PHARMACEUTICAL CO., LTD.

  公开号：EP1780210A1

  公开（公告）日：2007-05-02

  The present invention relates to cyclic amino benzoic acid derivatives which are effective in therapy of lipid metabolism abnormality, diabetes and the like as a human peroxisome proliferators-activated receptor (PPAR) agonist, in particular, as an agonist against human PPARα isoform, and addition salts thereof, and pharmaceutical compositions containing these compounds. A cyclic amino benzoic acid derivative represented by the general formula (1) [wherein a ring Ar represents an aryl group which may have substituent, or the like; Y represents a C1-C4 alkylene, C2-C4 alkenylene, C2-C4 alkynylene, or the like; Z represents an oxygen atom, sulfur atom or - (CH2)n- (n represents 0,1 or 2) ; X represents a hydrogen atom, halogen atom, lower alkyl group which may be substituted with a halogen atom, or the like; R represents a hydrogen atom or lower alkyl group, and -COOR substitutes for an ortho position or metha position of binding position of ring W] or a pharmaceutically acceptable salt thereof.

  本发明涉及作为人过氧化物酶体增殖激活受体（PPAR）激动剂，特别是作为人PPARα同工酶的激动剂，对脂质代谢异常、糖尿病等治疗有效的环氨基苯甲酸衍生物及其加成盐，以及含有这些化合物的药物组合物。 由通式（1）代表的环氨基苯甲酸衍生物 [其中，环 Ar 代表芳基，可具有取代基等；Y 代表 C1-C4 亚烷基、C2-C4 亚烯基、C2-C4 亚炔基等；Z 代表氧原子、硫原子或 - (CH2)n- （n 代表 0、1 或 2）；X 代表氢原子、卤素原子、可被卤素原子取代的低级烷基或类似物；R 代表氢原子或低级烷基，-COOR 取代环 W 结合位的正位或甲位]或其药学上可接受的盐。
• NOVEL CYCLIC AMINOPHENYLALKANOIC ACID DERIVATIVE
  申请人：Kyorin Pharmaceutical Co., Ltd.

  公开号：EP1862464A1

  公开（公告）日：2007-12-05

  The present invention provides cyclic aminophenylalkanoic acid derivatives that act as agonists for human peroxisome proliferator-activated receptors (PPARs), in particular human PPARα isoform, and are effective in the treatment of abnormal lipid metabolism, diabetes and other disorders. The present invention also provides addition salts of such cyclic aminophenylalkanoic acid derivatives and pharmaceutical compositions containing these compounds. Specifically, the present invention provides cyclic aminophenylalkanoic acid derivatives represented by the following general formula (1) : or pharmaceutically acceptable salts thereof.

  本发明提供的环氨基苯烷酸衍生物可作为人类过氧化物酶体增殖激活受体（PPARs），特别是人类 PPARα 同工型的激动剂，并可有效治疗脂质代谢异常、糖尿病和其他疾病。本发明还提供了此类环氨基苯烷酸衍生物的加成盐和含有这些化合物的药物组合物。 具体而言，本发明提供了由以下通式（1）代表的环氨基苯烷酸衍生物： 或其药学上可接受的盐类。