2-溴-1-[4-(2-氯乙基)苯基]乙酮 | 69614-96-6

• 分子结构分类: 有机化合物 - 有机氧化合物
• 中文名称: 2-溴-1-[4-(2-氯乙基)苯基]乙酮
• 英文名称: 2-Bromo-1-[4-(2-chloro-ethyl)-phenyl]-ethanone
• 英文别名: 2-Bromo-1-[4-(2-chloroethyl)phenyl]ethan-1-one；2-bromo-1-[4-(2-chloroethyl)phenyl]ethanone
• CAS: 69614-96-6
• 化学式: C₁₀H₁₀BrClO
• 分子量: 261.546
• InChiKey: YSDHRQRAVFIIQJ-UHFFFAOYSA-N

物化性质

• 熔点：
  41 °C(Solvent: Methanol)
• 沸点：
  343.4±27.0 °C(Predicted)
• 密度：
  1.466±0.06 g/cm3(Temp: 20 °C; Press: 760 Torr)(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  3.2
• 重原子数：
  13
• 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：
  17.1
• 氢给体数：
  0
• 氢受体数：
  1

反应信息

• 作为反应物：
  描述：

  2-溴-1-[4-(2-氯乙基)苯基]乙酮 在 sodium carbonate 、 N,N-二异丙基乙胺 、 sodium iodide 作用下， 以 丙酮 为溶剂， 反应 123.0h， 生成 4-(4-(2-(4-(1-Naphthyl)piperazinyl)ethyl)phenyl)-2-methylaminothiazole
  参考文献：
  名称：

  1-Naphthylpiperazine derivatives as potential atypical antipsychotic agents

  摘要：

  The design and synthesis of a series of potential atypical antipsychotic agents based on the structure of 1-naphthylpiperazine are described. The incorporation of dopamine antagonist activity into the parent structure was achieved with heterocyclic surrogates for the catechol moiety of dopamine. Compound 4b from this series showed a biochemical profile that translated to behavioral activity in the rat predictive of an antipsychotic agent with a low propensity to cause extrapyramidal side effects in man.

  DOI：

  10.1021/jm00110a016
• 作为产物：
  描述：

  4-(2-氯乙基)苯乙酮 在 溴 、 溶剂黄146 作用下， 反应 1.0h， 生成 2-溴-1-[4-(2-氯乙基)苯基]乙酮
  参考文献：
  名称：

  1-Naphthylpiperazine derivatives as potential atypical antipsychotic agents

  摘要：

  The design and synthesis of a series of potential atypical antipsychotic agents based on the structure of 1-naphthylpiperazine are described. The incorporation of dopamine antagonist activity into the parent structure was achieved with heterocyclic surrogates for the catechol moiety of dopamine. Compound 4b from this series showed a biochemical profile that translated to behavioral activity in the rat predictive of an antipsychotic agent with a low propensity to cause extrapyramidal side effects in man.

  DOI：

  10.1021/jm00110a016

文献信息

• [EN] PYRIDONE AND PYRIDAZINONE DERIVATIVES AS MCH ANTAGONISTS<br/>[FR] DÉRIVÉS DE PYRIDONE ET DE PYRIDAZINONE COMME ANTAGONISTES DE LA MCH
  申请人：BOEHRINGER INGELHEIM INT

  公开号：WO2009103478A1

  公开（公告）日：2009-08-27

  The present invention relates to pyridone and pyridazinone derivatives as listed in claim 1 including their salts. Moreover the invention relates to pharmaceutical compositions containing at least one compound according to the invention. By virtue of their MCH- receptor antagonistic activity the pharmaceutical compositions according to the invention are suitable for the treatment of metabolic disorders and/or eating disorders, particularly obesity, bulimia, anorexia, hyperphagia and diabetes.

  本发明涉及权利要求1中所列的吡啶酮和吡啶并二嗪酮衍生物及其盐。此外，本发明还涉及含有至少一种根据本发明的化合物的药物组合物。凭借其黑色素细胞刺激素受体拮抗活性，根据本发明的药物组合物适用于治疗代谢紊乱和/或饮食失调，特别是肥胖、贪食症、厌食症、过食和糖尿病。
• PYRIDYL SUBSTITUTED THIAZOLES
  申请人：——

  公开号：US20010000178A1

  公开（公告）日：2001-04-05

  Disclosed is a novel class of thiazole, thiadiazole, and oxadiazole compounds which are substituted at their nuclear carbons by aromatic moieties. These compounds exhibit antifungal activity against a variety of fungi including strains which have proven to be resistant to treatment with known antifungal agents such as Fluconazole.

  本发明涉及一类新型的噻唑、噻二唑和噁二唑化合物，其核碳被芳香基取代。这些化合物对多种真菌具有抗真菌活性，包括那些已被证明对已知抗真菌药物如氟康唑治疗产生抗药性的菌株。
• Novel class of thiomorpholino substituted thiazoles
  申请人：——

  公开号：US20010000177A1

  公开（公告）日：2001-04-05

  Disclosed is a novel class of thiazole, thiadiazole, and oxadiazole compounds which are substituted at their nuclear carbons by aromatic moieties. These compounds exhibit antifungal activity against a variety of fungi including strains which have proven to be resistant to treatment with known antifungal agents such as Fluconazole.

  本发明涉及一类新型的噻唑、噻二唑和噁二唑化合物，其核碳原子被芳香族基团取代。这些化合物对多种真菌表现出抗真菌活性，包括那些已被已知抗真菌药物如氟康唑治疗后仍然耐药的菌株。
• Novel class of piperazino substituted thiazoles
  申请人：——

  公开号：US20010000512A1

  公开（公告）日：2001-04-26

  Disclosed is a novel class of thiazole, thiadiazole, and oxadiazole compounds which are substituted at their nuclear carbons by aromatic moieties. These compounds exhibit antifungal activity against a variety of fungi including strains which have proven to be resistant to treatment with known antifungal agents such as Fluconazole.

  本发明涉及一类新型的噻唑、噻二唑和噁二唑化合物，它们的核碳被芳香族基替代。这些化合物对多种真菌表现出抗真菌活性，包括那些已被证明对已知的抗真菌药物如氟康唑的治疗具有抗药性的菌株。
• Thiadiazole antifungal agents
  申请人：——

  公开号：US20020002193A1

  公开（公告）日：2002-01-03

  Disclosed is a novel class of thiazole, thiadiazole, and oxadiazole compounds which are substituted at their nuclear carbons by aromatic moieties. These compounds exhibit antifungal activity against a variety of fungi including strains which have proven to be resistant to treatment with known antifungal agents such as Fluconazole.

  本发明涉及一种新型的噻唑、噻二唑和噁二唑化合物类，其核碳被芳香基团取代。这些化合物对各种真菌表现出抗真菌活性，包括那些已被证明对已知抗真菌药物如氟康唑治疗产生抗药性的菌株。