3-(3-氨基-4-氯苯基)丙酸甲酯 | 383669-60-1

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 中文名称: 3-(3-氨基-4-氯苯基)丙酸甲酯
• 英文名称: methyl 3-(3-amino-4-chlorophenyl)propanoate
• 英文别名: methyl 3-(3-amino-4-chlorophenyl)propionate
• CAS: 383669-60-1
• 化学式: C₁₀H₁₂ClNO₂
• 分子量: 213.664
• InChiKey: PUXJIEUFDFZLQY-UHFFFAOYSA-N

物化性质

• 沸点：
  313.7±27.0 °C(Predicted)
• 密度：
  1.235±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  2
• 重原子数：
  14
• 可旋转键数：
  4
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.3
• 拓扑面积：
  52.3
• 氢给体数：
  1
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  3-(3-氨基-4-氯苯基)丙酸甲酯 在 2-双环己基膦-2',6'-二甲氧基联苯 、 tris-(dibenzylideneacetone)dipalladium(0) 、 碘 、 silver sulfate 、 N,N-二异丙基乙胺 作用下， 以 四氢呋喃 、 甲醇 、 N,N-二甲基甲酰胺 为溶剂， 反应 4.1h， 生成 methyl (S)-3-(4-benzamido-5-chloro-2-(3-methoxy-3-oxopropyl)phenyl)-2-((tert-butoxycarbonyl)amino)propanoate
  参考文献：
  名称：

  Design, synthesis and in vitro pharmacology of GluK1 and GluK3 antagonists. Studies towards the design of subtype-selective antagonists through 2-carboxyethyl-phenylalanines with substituents interacting with non-conserved residues in the GluK binding sites

  摘要：

  In order to identify compounds selective for the GluK1 and GluK3 subtypes of kainate receptors we have designed and synthesized a series of (S)-2-amino-3-((2-carboxyethyl)phenyl)propanoic acid analogs with hydrogen bond donating and accepting substituents on the aromatic ring. Based on crystal structures of GluK1 in complex with related ligands, the compounds were designed to explore possible interactions with non-conserved residues outside the glutamate ligand binding site and challenge the water binding network. Apart from obtaining GluK1 selective antagonists one analog with a phenyl-substituted urea (compound 31) showed some preference for GluK3 over GluK1-receptors. Docking studies indicate that this preference may be attributed to contacts between the NH of the urea substituent and non-conserved Ser741 and Ser761 residues.

  DOI：

  10.1016/j.bmc.2014.07.045
• 作为产物：
  描述：

  tert-butyl (2E)-3-(4-chloro-3-nitrophenyl)acrylate 在 palladium 10% on activated carbon 氯化亚砜 、 氢气 作用下， 以 四氢呋喃 、 乙醇 为溶剂， 反应 13.5h， 生成 3-(3-氨基-4-氯苯基)丙酸甲酯
  参考文献：
  名称：

  SUBSTITUTED 3-PHENYLPROPIONIC ACIDS AND THE USE THEREOF

  摘要：

  本申请涉及新颖的3-苯丙酸衍生物，其制备方法，它们用于治疗和/或预防疾病的用途，以及它们用于制备治疗和/或预防疾病的药物的用途，特别是用于治疗和/或预防心血管疾病。

  公开号：

  US20110130445A1

文献信息

• Benzoxazepinones and their use as squalene synthase inhibitors
  申请人：——

  公开号：US20030078251A1

  公开（公告）日：2003-04-24

  There is disclosed a compound represented by the formula [I]: 1 wherein R 1 is optionally substituted 1-carboxyethyl group, optionally substituted alkyl-sulfonyl group, optionally substituted (carboxy-cycloalkyl)-alkyl group, —X 1 —X 2 —Ar—X 3 —X 4 —COOH (wherein X 1 and X 4 are a bond or alkylene group, X 2 and X 3 are a bond, —O—, —S—, Ar is divalent aromatic group etc.), R 2 is alkyl group optionally substituted with alkanoyloxy group and/or hydroxy group, R 3 is alkyl group, and W is halogen atom, etc., or a salt thereof. The compound has the cholesterol lowering activity and the triglyceride lowering activity and is useful for preventing and/or treating hyperlipidemia.

  披露了一种由公式[I]表示的化合物： 1 其中R 1 是可选地取代的1-羧乙基，可选地取代的烷基亚磺酰基，可选地取代的(羧基环烷基)-烷基，—X 1 —X 2 —Ar—X 3 —X 4 —COOH(其中X 1 和X 4 是键或亚烷基，X 2 和X 3 是键，—O—，—S—，Ar是二价芳香族等)，R 2 是可选地由酰氧基和/或羟基取代的烷基，R 3 是烷基，W是卤素原子等，或其盐。该化合物具有降低胆固醇活性和降低甘油三酯活性，用于预防或治疗高脂血症。
• Substituted 3-phenylpropionic acids and the use thereof
  申请人：Bayer Intellectual Property GmbH

  公开号：US09018414B2

  公开（公告）日：2015-04-28

  The present application relates to novel 3-phenylpropionic acid derivatives, to processes for their preparation, to their use for the treatment and/or prevention of diseases and to their use for preparing medicaments for the treatment and/or prevention of diseases, in particular for the treatment and/or prevention of cardiovascular disorders.

  本申请涉及新型3-苯丙酸衍生物，其制备方法，用于治疗和/或预防疾病的用途以及用于制备治疗和/或预防疾病的药物的用途，特别是用于治疗和/或预防心血管疾病的用途。
• BENZOXAZEPINONES AND THEIR USE AS SQUALENE SYNTHASE INHIBITORS
  申请人：Takeda Chemical Industries, Ltd.

  公开号：EP1292585A1

  公开（公告）日：2003-03-19
• SUBSTITUIERTE 3-PHENYLPROPIONSÄUREN UND IHRE VERWENDUNG
  申请人：Bayer Pharma Aktiengesellschaft

  公开号：EP2493845A1

  公开（公告）日：2012-09-05
• US9018414B2
  申请人：——

  公开号：US9018414B2

  公开（公告）日：2015-04-28