3-chloro-1-(5-fluorobenzo[b]thiophen-3-yl)propan-1-one | 344764-43-8

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 苯并噻吩类
• 英文名称: 3-chloro-1-(5-fluorobenzo[b]thiophen-3-yl)propan-1-one
• 英文别名: 3-chloro-1-(5-fluorobenzo[b]thiophenyl)propanone；(5-fluorobenzo[b]thiophen-3-yl)-3-chloropropan-1-one；3-chloro-1-(5-fluoro-1-benzothien-3-yl)propan-1-one；3-chloro-1-(5-fluoro-1-benzothiophen-3-yl)propan-1-one
• CAS: 344764-43-8
• 化学式: C₁₁H₈ClFOS
• 分子量: 242.701
• InChiKey: HICUGZLLPZOJAH-UHFFFAOYSA-N

物化性质

• 沸点：
  377.4±32.0 °C(Predicted)
• 密度：
  1.373±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  3.2
• 重原子数：
  15
• 可旋转键数：
  3
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.18
• 拓扑面积：
  45.3
• 氢给体数：
  0
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  3-chloro-1-(5-fluorobenzo[b]thiophen-3-yl)propan-1-one 在 sodium tetrahydroborate 、 potassium carbonate 作用下， 以 四氢呋喃 、 甲醇 为溶剂， 反应 73.0h， 生成 1-(5-fluorobenzo[b]thiophen-3-yl)-3-[4-(indol-4-yl)piperazin-1-yl]propan-1-ol
  参考文献：
  名称：

  合成和分子建模的新的1-芳基-3- [4-芳基哌嗪-1-基] -1-丙烷衍生物在5-羟色胺转运蛋白和5-HT（1A）受体上具有高亲和力。

  摘要：

  有人提出5-HT（1A）受体拮抗剂可增强选择性5-羟色胺（5-HT）再摄取抑制剂的抗抑郁功效。为了寻求新型有效的抗抑郁药，设计，合成了1-（芳基）-3- [4-芳基哌嗪-1-基] -1-丙烷分子杂化物，并对其5-HT再摄取抑制和5-HT（ 1A）受体亲和力。该设计基于偶联与抑制5-羟色胺再摄取有关的结构部分，例如苯并[b]噻吩衍生物与典型的5-HT（1A）受体配体芳基哌嗪。在结合研究中，几种化合物对5-HT转运蛋白和5-HT（1A）受体表现出亲和力。分子模型研究预测了高亲和力结合所需的药效基团元素，以及能够区分激动剂，部分激动剂，或对5-HT（1A）受体的拮抗作用和对5-HT转运蛋白的抑制。在结合步骤之前，去溶剂化过程中的溶剂相互作用以及焓和人类补偿可能是解释激动剂，部分激动剂和拮抗剂特性的原因。氢键键合能力似乎很重要，可以打破氢螺旋间的氢键或在配体结合后形成其他键。部分激动剂和拮抗剂不能

  DOI：

  10.1021/jm0111200
• 作为产物：
  描述：

  5-氟苯并[b]噻吩 、 3-氯丙酰氯 在 aluminum (III) chloride 作用下， 以 氯仿 为溶剂， 以46%的产率得到3-chloro-1-(5-fluorobenzo[b]thiophen-3-yl)propan-1-one
  参考文献：
  名称：

  [EN] 3-AMINO CHOMAN AND 2-AMINO TETRALIN DERIVATIVES
  [FR] DERIVES 3-AMINO CHOMANE ET 2-AMINO TETRALINE

  摘要：

  揭示了3-氨基色苷和2-氨基四氢萘衍生物以及含有这些化合物的组合物。还揭示了在治疗血清素失调症，如抑郁症和焦虑症中使用3-氨基色苷和2-氨基四氢萘化合物以及含有这些化合物的组合物的方法。

  公开号：

  WO2005012291A1

文献信息

• Benzothiophene derivative compounds process of preparation and use thereof
  申请人：——

  公开号：US20040034219A1

  公开（公告）日：2004-02-19

  This invention provides new benzothiophene derivatives of general formula (I) and a process for preparing them, the corresponding compositions and their use for manufacturing a medicine for the treatment of neurological disorders. These new compounds behave as serotonin reuptake inhibitors and show high affinity towards the 5-HT 1A receptor.

  本发明提供了一种新的苯并噻吩衍生物通式（I）及其制备方法、相应的组合物以及它们用于制造治疗神经系统疾病的药物。这些新化合物具有作为5-HT1A受体的血清素再摄取抑制剂的行为，并表现出高亲和力。
• 3-Amino chroman and 2-amino tetralin derivatives
  申请人：Hatzenbuhler Theriault Nicole

  公开号：US20050032873A1

  公开（公告）日：2005-02-10

  3-Amino chroman and 2-amino tetralin derivatives and compositions containing such compounds are disclosed. Methods of using the 3-amino chroman and 2-amino tetralin compounds and compositions containing such compounds in the treatment of serotonin disorders, such as depression and anxiety, are also disclosed.

  本文披露了3-氨基色满和2-氨基四氢萘衍生物及含有这些化合物的组合物。还披露了使用3-氨基色满和2-氨基四氢萘化合物及含有这些化合物的组合物治疗血清素失调症，如抑郁和焦虑的方法。
• Novel Benzo[<i>b</i>]thiophene Derivatives as New Potential Antidepressants with Rapid Onset of Action
  作者：Luis Berrade、Bárbara Aisa、María J. Ramirez、Silvia Galiano、Salvatore Guccione、Lise Román Moltzau、Finn Olav Levy、Ferdinando Nicoletti、Giuseppe Battaglia、Gemma Molinaro、Ignacio Aldana、Antonio Monge、Silvia Perez-Silanes

  DOI：10.1021/jm2000773

  日期：2011.4.28

  We report benzo[b]thiophene derivatives synthesized according 10 a dual strategy. 8j, 9c, and 9e with affinity values toward 5-HT(7)R and 5-HTT were selected to probe their antidepressant activity in vivo using the forced swimming text (FST). The results slowed significant antidepressant activity after chronic treatment. 9c was effective in reducing the immobility time in FST even after acute treatment. These findings identify these compounds as a new class of antidepressants with a rapid onset of action.
• New 3-[4-(aryl)piperazin-1-yl]-1-(benzo[b]thiophen-3-yl)propane derivatives with dual action at 5-HT1A serotonin receptors and serotonin transporter as a new class of antidepressants
  作者：J Martínez

  DOI：10.1016/s0223-5234(00)01198-3

  日期：2001.1

  A series of new 3-[4-(aryl)piperazin-1-yl]-1-(benzo[b]thiophen-3-yl)propane derivatives were synthesized in an attempt to find a new class of antidepressant drugs with dual activity at 5-HT1A serotonin receptors and serotonin transporter. Title compounds were evaluated for in vitro activity on 5-HT1A receptor and 5-HT transporter. They show high nanomolar affinity for both activities, and in particular, compounds 1-(5-chlorobenzo[b]thiophen-3-yl)-3-[4-(2-methoxyphenyl)piperazin-1-yl]propan-1-ol (7) and 1-(5-fluorobenzo[b]thiophen-3-yl)-3-[4-(2-methoxyphenyl) piperain-1-yl]propan-1-ol (8) show values (nM) of K-i = 30 and 2.3 for 5-HT1A receptors and K-i = 30 and 12 for serotonin transporters, respectively. In GTP gammaS binding assays, compound 8 revealed antagonist properties to 5-HT1A receptors. Such a pharmacological profile could lead to potent antidepressant agents with new dual mechanism of action. (C) 2001 Editions scientifiques et medicales Elsevier SAS.
• BENZOTHIOPHENE DERIVATIVE COMPOUNDS, PROCESS OF PREPARATION AND USE THEREOF
  申请人：LABORATORIOS VITA, S.A.

  公开号：EP1337528B1

  公开（公告）日：2004-08-04