3-(乙酰氨基)-1,2,3,4-四氢-2-氧代-乙酯-3-喹啉羧酸 | 61548-64-9

• 分子结构分类: 有机化合物 - 有机酸及其衍生物 - 羧酸及其衍生物
• 中文名称: 3-(乙酰氨基)-1,2,3,4-四氢-2-氧代-乙酯-3-喹啉羧酸
• 英文名称: ethyl 3-acetamido-2-oxo-1,2,3,4-tetrahydroquinoline-3-carboxylate
• 英文别名: ethyl 3-acetamido-2-oxo-1,4-dihydroquinoline-3-carboxylate
• CAS: 61548-64-9
• 化学式: C₁₄H₁₆N₂O₄
• 分子量: 276.292
• InChiKey: HQKXRBPZRHVZQH-UHFFFAOYSA-N

物化性质

• 熔点：
  186.5-188 °C
• 沸点：
  537.3±50.0 °C(Predicted)
• 密度：
  1.28±0.1 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  0.8
• 重原子数：
  20
• 可旋转键数：
  4
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.36
• 拓扑面积：
  84.5
• 氢给体数：
  2
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  3-(乙酰氨基)-1,2,3,4-四氢-2-氧代-乙酯-3-喹啉羧酸 在 盐酸 作用下， 以 水 为溶剂， 反应 6.0h， 生成 3-amino-1,2,3,4-tetrahydroquinolin-2-one
  参考文献：
  名称：

  (4 + 2) cyclization of aza-o-quinone methides with azlactones: construction of biologically important dihydroquinolinone frameworks

  摘要：

  使用azlactones对N-(o-氯甲基)芳基酰胺进行碱促进的(4 + 2)环化反应，可以高产率地构建生物学上重要的二氢喹啉酮骨架。

  DOI：

  10.1039/d0ob02388d
• 作为产物：
  描述：

  diethyl 2-acetamido-2-(2-nitrobenzyl)malonate 在 铁粉 、 氯化铵 作用下， 以 四氢呋喃 、 乙醇 为溶剂， 反应 3.5h， 以89%的产率得到3-(乙酰氨基)-1,2,3,4-四氢-2-氧代-乙酯-3-喹啉羧酸
  参考文献：
  名称：

  [EN] 1,2,3,4-TETRAHYDROQUINOLINE DERIVATIVES AS INHIBITORS OF THE YAP/TAZ-TEAD ACTIVATION FOR TREATING CANCER
  [FR] DÉRIVÉS DE 1,2,3,4-TÉTRAHYDROQUINOLINE SERVANT D'INHIBITEURS DE L'ACTIVATION DE YAP/TAZ-TEAD POUR LE TRAITEMENT DU CANCER

  摘要：

  本发明涉及化合物（la）的新颖化合物，以及将该化合物用作药物，更具体地用于预防或治疗由YAP / TAZ-TEAD转录活性介导的疾病，更具体地用于预防或治疗癌症或纤维化。本发明还涉及一种预防或治疗该疾病的方法，包括使用新颖化合物。本发明还涉及新颖化合物的药物组成物或组合制剂，以及将该组成物或制剂用作药物，更具体地用于预防或治疗由YAP / TAZ-TEAD转录活性介导的疾病，更具体地用于预防或治疗癌症或纤维化。本发明还涉及制备该化合物的方法。

  公开号：

  WO2022072741A1

文献信息

• Cycloalkyl, lactam, lactone and related compounds, pharmaceutical compositions comprising same, and methods for inhibiting beta-amyloid peptide release and/or its synthesis by use of such compounds
  申请人：——

  公开号：US20020045747A1

  公开（公告）日：2002-04-18

  Disclosed are compounds which inhibit &bgr;-amyloid peptide release and/or its synthesis, and, accordingly, have utility in treating Alzheimer's disease. Also disclosed are pharmaceutical compositions comprising a compound which inhibits &bgr;-amyloid peptide release and/or its synthesis as well as methods for treating Alzheimer's disease both prophylactically and therapeutically with such pharmaceutical compositions.

  公开了抑制β-淀粉样肽释放和/或其合成的化合物，因此可用于治疗阿尔茨海默病。还公开了包含抑制β-淀粉样肽释放和/或其合成的化合物的药物组合物，以及使用这些药物组合物预防性和治疗性治疗阿尔茨海默病的方法。
• Heterocyclic compounds, pharmaceutical compositions comprising same, and methods for inhibiting &bgr;-amyloid peptide release and/or its synthesis by use of such compounds
  申请人：Athena Neurosciences, Inc.

  公开号：US06506782B1

  公开（公告）日：2003-01-14

  Disclosed are compounds which inhibit &bgr;-amyloid peptide release and/or its synthesis, and, accordingly, have utility in treating Alzheimer's disease. Also disclosed are pharmaceutical compositions comprising a compound which inhibits &bgr;-amyloid peptide release and/or its synthesis as well as methods for treating Alzheimer's disease both prophylactically and therapeutically with such pharmaceutical compositions.

  公开了抑制β-淀粉样肽释放和/或其合成的化合物，因此可用于治疗阿尔茨海默病。还公开了包含抑制β-淀粉样肽释放和/或其合成的化合物的药物组合物，以及使用这些药物组合物预防性和治疗性地治疗阿尔茨海默病的方法。
• [EN] 4- BROMO - 5 - (2- CHLORO - BENZOYLAMINO) - 1H - PYRAZOLE - 3 - CARBOXYLIC ACID AMIDE DERIVATIVES AND RELATED COMPOUNDS AS BRADYKININ B1 RECEPTOR ANTAGONISTS FOR THE TREATMENT OF INFLAMMATORY DISEASES<br/>[FR] DERIVES AMIDES DE L'ACIDE CARBOXYLIQUE DE 4- BROMO - 5 - (2- CHLORO - BENZOYLAMINO) - 1H - PYRAZOLE 3 ET COMPOSES ASSOCIES EN TANT QU'ANTAGONISTES DE RECEPTEUR DE B1 DE LA BRADYKININE POUR LE TRAITEMENT DE MALADIES INFLAMMATOIRES
  申请人：ELAN PHARM INC

  公开号：WO2004098589A1

  公开（公告）日：2004-11-18

  Disclosed are compounds of formula I and II that are bradykinin B1 receptor antagonists and are useful for treating diseases, or relieving adverse symptoms associated with disease conditions, in mammals mediated by bradykinin B1 receptor. Certain of the compounds exhibit increased potency and are also expected to exhibit increased duration of action.

  公开的是化合物I和II的结构式，它们是激肽酶B1受体拮抗剂，适用于治疗哺乳动物中由激肽酶B1受体介导的疾病，或缓解与疾病状况相关的不良症状。其中某些化合物表现出增强的效力，并且预计还将表现出延长作用的特性。
• [EN] 1,2,3,4-TETRAHYDROQUINOLINE DERIVATIVES AS INHIBITORS OF THE YAP/TAZ-TEAD ACTIVATION FOR TREATING CANCER<br/>[FR] DÉRIVÉS DE 1,2,3,4-TÉTRAHYDROQUINOLINE SERVANT D'INHIBITEURS DE L'ACTIVATION DE YAP/TAZ-TEAD POUR LE TRAITEMENT DU CANCER
  申请人：UNIV LEUVEN KATH

  公开号：WO2022072741A1

  公开（公告）日：2022-04-07

  The present invention relates to novel compounds of formula (la), to said compounds for use as a medicine, more in particular for the prevention or treatment of diseases mediated by activity of YAP/ TAZ-TEAD transcription, yet more in particular for the prevention or treatment of cancer or fibrosis. The present invention also relates to a method for the prevention or treatment of said diseases comprising the use of the novel compounds. The present invention furthermore relates to pharmaceutical compositions or combination preparations of the novel compounds as well as to said compositions or preparations for use as a medicine, more preferably for the prevention or treatment of diseases mediated by activity of YAP/ TAZ-TEAD transcription, yet more in particular for the prevention or treatment of cancer or fibrosis. The present invention also relates to processes for the preparation of said compounds.

  本发明涉及化合物（la）的新颖化合物，以及将该化合物用作药物，更具体地用于预防或治疗由YAP / TAZ-TEAD转录活性介导的疾病，更具体地用于预防或治疗癌症或纤维化。本发明还涉及一种预防或治疗该疾病的方法，包括使用新颖化合物。本发明还涉及新颖化合物的药物组成物或组合制剂，以及将该组成物或制剂用作药物，更具体地用于预防或治疗由YAP / TAZ-TEAD转录活性介导的疾病，更具体地用于预防或治疗癌症或纤维化。本发明还涉及制备该化合物的方法。
• Cycloalkyl, lactam, lactone and related compounds, pharmaceutical compositions comprising same, and methods for inhibiting B-amyloid peptide release and/or its synthesis by use of such compounds
  申请人：——

  公开号：US20020173504A1

  公开（公告）日：2002-11-21

  Disclosed are compounds which inhibit &bgr;-amyloid peptide release and/or its synthesis, and, accordingly, have utility in treating Alzheimer's disease. Also disclosed are pharmaceutical compositions comprising a compound which inhibits &bgr;-amyloid peptide release and/or its synthesis as well as methods for treating Alzheimer's disease both prophylactically and therapeutically with such pharmaceutical compositions.

  本发明涉及抑制&bgr;-淀粉样肽的释放和/或合成的化合物，因此具有治疗阿尔茨海默病的效用。还公开了包含抑制&bgr;-淀粉样肽释放和/或合成的化合物的药物组合物，以及使用这种药物组合物预防和治疗阿尔茨海默病的方法。