1,2-dihydrobenzo[b]cyclopenta[d]thiophen-3-one | 10245-84-8

• 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: 1,2-dihydrobenzo[b]cyclopenta[d]thiophen-3-one
• 英文别名: 2,3-dihydro-1H-benzocyclopentathiophen-3-one；1H-Cyclopentathianaphthen-3(2H)-on；1,2-Dihydro-3-oxo-3H-cyclopenta<1>benzothiophen；1,2-Dihydro-benzo[b]cyclopenta[d]thiophen-3-on；7-Thiatricyclo[6.4.0.02,6]dodeca-1(8),2(6),9,11-tetraen-5-one；1,2-dihydrocyclopenta[b][1]benzothiol-3-one
• CAS: 10245-84-8
• 化学式: C₁₁H₈OS
• 分子量: 188.25
• InChiKey: JVCDJDYBTQSTNM-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3
• 重原子数：
  13
• 可旋转键数：
  0
• 环数：
  3.0
• 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：
  2

反应信息

• 作为反应物：
  描述：

  1,2-dihydrobenzo[b]cyclopenta[d]thiophen-3-one 生成 12H-benzo[4',5']thieno[3',2':4,5]cyclopenta[1,2-b]quinoline
  参考文献：
  名称：

  Cagniant, Bulletin de la Societe Chimique de France, 1949, p. 382,387

  摘要：

  DOI：
• 作为产物：
  描述：

  3-(苯并[b]噻吩-3-基)丙酸 在 二硫化碳 、 氯化亚砜 、 氯仿 、 四氯化锡 作用下， 生成 1,2-dihydrobenzo[b]cyclopenta[d]thiophen-3-one
  参考文献：
  名称：

  Cagniant; Cagniant, Bulletin de la Societe Chimique de France, 1953, p. 185,190

  摘要：

  DOI：

文献信息

• [EN] PYRIDONE AND AZA-PYRIDONE COMPOUNDS AND METHODS OF USE<br/>[FR] COMPOSÉS DE PYRIDONE ET D'AZA-PYRIDONE ET LEURS PROCÉDÉS D'UTILISATION
  申请人：GILEAD CONNECTICUT INC

  公开号：WO2011140488A1

  公开（公告）日：2011-11-10

  Pyridone and aza-pyridone compounds of Formula I are provided, including stereoisomers, tautomers, and pharmaceutically acceptable salts thereof, useful for inhibiting Btk kinase, and for treating immune disorders such as inflammation mediated by Btk kinase. Methods of using compounds of Formula I for in vitro, in situ, and in vivo diagnosis, and treatment of such disorders in mammalian cells, or associated pathological conditions, are disclosed.

  提供了公式I的吡啶酮和氮杂吡啶酮化合物，包括其立体异构体、互变异构体和药学上可接受的盐，用于抑制Btk激酶，并用于治疗由Btk激酶介导的炎症等免疫紊乱。公开了使用公式I化合物进行体外、原位和体内诊断以及治疗哺乳动物细胞中的这类紊乱或相关病理条件的方法。
• Efficient One-Pot Synthesis of Cyclopenta[b]thiophen-1-ones and 1,3-Di(2-thiophenyl)propan-1-ones from Thiophenes
  作者：Ivan L. Baraznenok、Valentine G. Nenajdenko、Elizabeth S. Balenkova

  DOI：10.1055/s-1997-1207

  日期：1997.4

  The reaction of N,N-dimethylacrylamide/triflic anhydride complex with substituted thiophenes led to the corresponding cyclopenta[b]thiophen-1-ones and 1,3-di(2-thiophenyl)propan-1-ones. The application of 2-bromo-N,N-dimethylacrylamide in this reaction allows 2-bromo-substituted five- or seven-membered thiophene-fused cyclic ketones to be obtained.

  N,N-二甲基丙烯酰胺/三氟乙酸酐复合物与取代噻吩的反应产生了相应的环戊[b]噻吩-1-酮和1,3-二(2-噻吩基)丙酮。该反应中使用2-溴-N,N-二甲基丙烯酰胺能够获得2-溴取代的五元或七元噻吩融合环酮。
• Synthetic studies of novel ninhydrin analogs
  作者：Richard R Hark、Diane B Hauze、Olga Petrovskaia、Madeleine M Joullié

  DOI：10.1139/v01-143

  日期：2001.11.1

  Ninhydrin is an essential tool in the analysis of amino acids, peptides, and proteins, and the preferred re - agent for the detection of latent fingerprints on porous surfaces. The goal of this investigation was to prepare ninhydrin analogs with enhanced chromogenic and fluorogenic properties. Target compounds included structures with extended conjugation and (or) with the presence of sulfur-containing

  茚三酮是分析氨基酸、肽和蛋白质的重要​​工具，也是检测多孔表面潜在指纹的首选试剂。本研究的目的是制备具有增强的显色和荧光特性的茚三酮类似物。目标化合物包括具有扩展共轭和（或）存在含硫部分的结构。我们已经为用作氨基酸检测试剂的新型杂环和芳基取代茚三酮类似物设计了一般收敛路线。
• PYRIDONE AND AZA-PYRIDONE COMPOUNDS AND METHODS OF USE
  申请人：BARBOSA Antonio J.M.

  公开号：US20120010191A1

  公开（公告）日：2012-01-12

  Pyridone and aza-pyridone compounds of Formula I are provided, including stereoisomers, tautomers, and pharmaceutically acceptable salts thereof, useful for inhibiting Btk kinase, and for treating immune disorders such as inflammation mediated by Btk kinase. Methods of using compounds of Formula I for in vitro, in situ, and in vivo diagnosis, and treatment of such disorders in mammalian cells, or associated pathological conditions, are disclosed.

  本发明提供公式I的吡啶酮和氮杂吡啶酮化合物，包括立体异构体、互变异构体和其医药上可接受的盐，用于抑制Btk激酶并治疗由Btk激酶介导的免疫紊乱，例如炎症。本发明还公开了使用公式I化合物在哺乳动物细胞中进行体外、原位和体内诊断和治疗此类疾病或相关病理条件的方法。
• Pyridone and aza-pyridone compounds and methods of use
  申请人：Barbosa Antonio J. M.

  公开号：US08618107B2

  公开（公告）日：2013-12-31

  Pyridone and aza-pyridone compounds of Formula I are provided, including stereoisomers, tautomers, and pharmaceutically acceptable salts thereof, useful for inhibiting Btk kinase, and for treating immune disorders such as inflammation mediated by Btk kinase. Methods of using compounds of Formula I for in vitro, in situ, and in vivo diagnosis, and treatment of such disorders in mammalian cells, or associated pathological conditions, are disclosed.

  本发明提供了公式I的吡啶酮和氮杂吡啶酮化合物，包括立体异构体、互变异构体和其药学上可接受的盐，用于抑制Btk激酶和治疗由Btk激酶介导的免疫紊乱，如炎症。本发明还揭示了使用公式I化合物进行哺乳动物细胞中的体外、原位和体内诊断和治疗这种疾病或相关病理情况的方法。