6-(3-chloropropyl)benzo[d]thiazol-2(3H)-one | 135792-95-9

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 苯并噻唑类
• 英文名称: 6-(3-chloropropyl)benzo[d]thiazol-2(3H)-one
• 英文别名: 6-(3-chloropropyl)-3H-1,3-benzothiazol-2-one
• CAS: 135792-95-9
• 化学式: C₁₀H₁₀ClNOS
• 分子量: 227.714
• InChiKey: DEDTZRIXJDBVGF-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3
• 重原子数：
  14
• 可旋转键数：
  3
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.3
• 拓扑面积：
  54.4
• 氢给体数：
  1
• 氢受体数：
  2

反应信息

• 作为反应物：
  描述：

  6-(3-chloropropyl)benzo[d]thiazol-2(3H)-one 在 CuCN potassium cyanide 、 NaCN 作用下， 以 N-甲基乙酰胺 、 氯仿 为溶剂， 生成 6-(3-cyanopropyl)benzothiazolinone
  参考文献：
  名称：

  New substituted benzothiazolinones

  摘要：

  通式（I）的化合物：##STR1## 其中：R.sub.1代表氢原子或较低的烷基基团，R.sub.2代表取代或未取代的烷基、苯基或取代或未取代的杂环基，它们的对映异构体、顺反异构体和外消旋体以及它们与药用可接受碱的加合物，当R.sub.1代表氢原子或R.sub.2包括羧酸基团时。药物产品。

  公开号：

  US05084469A1
• 作为产物：
  描述：

  6-(3-chloropropanoyl)-3-methylbenzothiazol-2(3H)-one 以84%的产率得到6-(3-chloropropyl)benzo[d]thiazol-2(3H)-one
  参考文献：
  名称：

  Aminoalkyl benzothiazolinones

  摘要：

  该发明涉及化合物的公式(I)：##STR1##其中R.sub.1和R.sup.2如描述中定义，其光学异构体，以及与药学上可接受的酸或碱形成的加合盐，以及用于治疗患有与西格玛受体相关疾病的哺乳动物的药用产品。

  公开号：

  US05512569A1

文献信息

• Mild and Versatile Potassium Fluoride/Tetrabutylammonium Fluoride Protocol for Ester Hydrolysis
  作者：D. Vijayalakshmi、K. Balakrishna、Shaik Mustafa

  DOI：10.14233/ajchem.2018.20937

  日期：——

  A mild and versatile protocol of potassium fluoride/tetrabutylammonium fluoride (KF/TBAF) in aqueous tetrahydrofuran for ester hydrolysis has been developed. The method is applied on variety of aliphatic and aromatic ester moieties bearing acid or base sensitive functional groups. The conditions have been also applied on acetates to yield alcohols. The chirality of optically pure esters remained intact with the conditions of the reaction.

  我们开发了一种在四氢呋喃水溶液中使用氟化钾/四丁基氟化铵（KF/TBAF）进行酯水解的温和且多功能的方法。该方法适用于含有酸或碱敏感官能团的各种脂肪族和芳香族酯。该方法还可用于醋酸酯类以生成醇类。在反应条件下，光学纯酯的手性保持不变。
• Novel Benzothiazolin-2-one and Benzoxazin-3-one Arylpiperazine Derivatives with Mixed 5HT_1A/D₂ Affinity as Potential Atypical Antipsychotics
  作者：Thierry Taverne、Ousmane Diouf、Patrick Depreux、Jacques H. Poupaert、Daniel Lesieur、Béatrice Guardiola-Lemaître、Pierre Renard、Marie-Claire Rettori、Daniel-Henri Caignard、Bruno Pfeiffer

  DOI：10.1021/jm970298c

  日期：1998.6.1

  (5HT1A agonism or 5HT2A antagonism) combined with D2 antagonism may lead to atypical antipsychotic drugs, a series of 19 benzothiazolin-2-one and benzoxazin-3-one derivatives possessing the arylpiperazine moiety was prepared, and their binding profiles were investigated. All tested compounds displayed very high affinities for the 5HT1A and D2 receptors. Therefore, further pharmacological studies were carried

  由于已知5HT特性（5HT1A拮抗作用或5HT2A拮抗作用）与D2拮抗作用相结合可导致非典型抗精神病药，因此制备了一系列19个具有芳基哌嗪部分的苯并噻唑啉-2-酮和苯并恶嗪-3-酮衍生物，并制备了它们的衍生物。结合概况进行了调查。所有测试的化合物均对5HT1A和D2受体表现出非常高的亲和力。因此，对选定的化合物（24、27、30、46和47）进行了进一步的药理研究。在大鼠中的这一评估清楚地表明了强效抗精神病药物的特性以及锥体束外副作用的减少。这些衍生物目前正在临床前开发中。
• HIGHLY SELECTIVE SIGMA RECEPTOR RADIOLIGANDS
  申请人：McCurdy Christopher R.

  公开号：US20110280804A1

  公开（公告）日：2011-11-17

  Compounds having the general formula III′, or IV′ wherein R 1 can be a radical of an optionally substituted C-4 to C-7 N-containing heterocycle or a radical of an optionally substituted cyclic or acyclic tertiary amine or isoindoline-1,3-dione: R 2,4,5,6 can each independently be any one or combinations of the following moieties, cyano, nitro, acyl, alkyl, amido, azido, isothiocyanate, isocyanate, optionally substituted anilino, halogens, ethers, sulfonamides, thioacyl, nitro, aromatic, heterocyclic, olefinic, acetylene, deuterium, or tritium; Y is S; Z can be either H, O, S, S—R or NR where R groups can be either H, aryls, alkyls, or cycloalkyls; “n” can be 1 to 5 carbons in length and stereoisomers, functional analogs, and pharmaceutically acceptable salts thereof and wherein the moiety bridging R 1 and N can be a substituted alkylene, optionally substituted alkenylene or optionally substituted alkynylene and where the alkylene group can include an inserted C 3 -C 5 cycloalkyl group, aromatic, and heterocyclic group; and wherein X is C 1 -C 4 radiohaloalkyl.

  具有通式III'或IV'的化合物，其中R1可以是一个可选取代的C-4到C-7含氮杂环的基团，或者是一个可选取代的环状或非环状三级胺或异吲哚啉-1,3-二酮的基团；R2、4、5、6可以各自独立地是以下任何一种或组合：氰基、硝基、酰基、烷基、酰胺基、偶氮基、异硫氰酸酯基、异氰酸酯基、可选取代的苯胺基、卤素、醚、磺酰胺基、硫代酰基、芳香族、杂环、烯烃、乙炔、氘或氚；Y是S；Z可以是H、O、S、S-R或NR，其中R基团可以是H、芳基、烷基或环烷基；“n”可以是1到5个碳原子，包括立体异构体、功能类似物和药物可接受的盐；其中桥接R1和N的基团可以是取代的烷基、可选取代的烯基或可选取代的炔基，其中烷基可以包括插入的C3-C5环烷基、芳香族和杂环基团；X为C1-C4放射性卤代烷基。
• HIGHLY SELECTIVE SIGMA RECEPTOR LIGANDS AND RADIOLIGANDS AS PROBES IN NOCICEPTIVE PROCESSING AND THE PATHPHYSIOLOGICAL STUDY OF MEMORY DEFICITS AND COGNITIVE DISORDERS
  申请人：The Board of Trustees of the Leland Stanford Junior University

  公开号：US20140328755A1

  公开（公告）日：2014-11-06

  A method for localizing and quantifying S1R role in nociceptive processing; for providing a guide to providing an analgesic therapy; of using an S1R selective ligand as a biomarker for pathphysiological study of memory deficits and cognitive disorders; or of detecting increased S1R density at the site of nerve injury arising from neuropathic pain comprising using as a probe at least one SR1 selective compound or radioligand of the general formula III′, or IV′:

  一种定位和量化S1R在伤害处理中的作用的方法；为提供镇痛疗法提供指导；使用S1R选择性配体作为记忆缺陷和认知障碍的病理生理研究的生物标志物；或者使用至少一种SR1选择性化合物或放射性配体作为探针，检测神经病理性疼痛引起的神经损伤部位的S1R密度增加，其化学结构为通式III'或IV'。
• Improved protocol for the radiosynthesis of [ ¹⁸ F]FTC‐146: A potent and selective sigma‐1 receptor radioligand
  作者：Masoud Sadeghzadeh、Barbara Wenzel、Julia Nikodemus、Alexandru Florea、Fabian Hertel、Klaus Kopka、Andreas T. J. Vogg、Fabian Kiessling、Felix M. Mottaghy

  DOI：10.1002/jlcr.4018

  日期：2023.3

  [18F]FTC-146 was introduced as a very potent and selective sigma-1 receptor radioligand, which has shown promising application as an imaging agent for neuropathic pain with positron emission tomography. In line with a multi-laboratory project on animal welfare, we chose this radioligand to investigate its potential for detecting neuropathic pain and tissue damage in tumor-bearing animals. However, the radiochemical yield (RCY) of around 4–7% was not satisfactory to us, and efforts were made to improve it. Herein, we describe an improved approach for the radiosynthesis of [18F]FTC-146 resulting in a RCY, which is sevenfold higher than that previously reported. A tosylate precursor was synthesized and radio-fluorination experiments were performed via aliphatic nucleophilic substitution reactions using either K[18F]F-Kryptofix®222 (K2.2.2)-carbonate system or tetra-n-butylammonium [18F]fluoride ([18F]TBAF). Several parameters affecting the radiolabeling reaction such as solvent, 18F-fluorination agent with the corresponding amount of base, labeling time, and temperature were investigated. Best labeling reaction conditions were found to be [18F]TBAF and acetonitrile as solvent at 100°C. The new protocol was then translated to an automated procedure using a FX2 N synthesis module. Finally, the radiotracer reproducibly obtained with RCYs of 41.7 ± 4.4% in high radiochemical purity (>98%) and molar activities up to 171 GBq/μmol.

  [18F]FTC-146是一种非常有效且具有选择性的sigma-1受体放射性配体，它作为正电子发射断层扫描神经病理性疼痛成像剂的应用前景广阔。为了配合一个有关动物福利的多实验室项目，我们选择了这种放射性配体来研究它在检测肿瘤动物的神经病理性疼痛和组织损伤方面的潜力。然而，4-7%左右的放射化学收率（RCY）并不能令我们满意，因此我们一直在努力改进。在此，我们介绍了一种改进的[18F]FTC-146 辐射合成方法，其 RCY 比以前报道的方法高出七倍。我们合成了一种对甲苯磺酸盐前体，并使用 K[18F]F-Kryptofix®222 (K2.2.2)-carbonate 体系或[18F]氟化四正丁基铵（[18F]TBAF）通过脂肪族亲核取代反应进行了放射性氟化实验。研究了影响放射性标记反应的几个参数，如溶剂、18F-氟化剂与相应量的碱基、标记时间和温度。结果发现，[18F]TBAF 和乙腈作为溶剂，温度为 100°C，是最佳的标记反应条件。然后，使用 FX2 N 合成模块将新方案转化为自动程序。最后，放射性示踪剂以高放射化学纯度（>98%）和最高 171 GBq/μmol 的摩尔活度重复获得，RCYs 为 41.7 ± 4.4%。