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5-(1-Benzothiophen-2-yl)furan-2-carbaldehyde

中文名称
——
中文别名
——
英文名称
5-(1-Benzothiophen-2-yl)furan-2-carbaldehyde
英文别名
——
5-(1-Benzothiophen-2-yl)furan-2-carbaldehyde化学式
CAS
——
化学式
C13H8O2S
mdl
——
分子量
228.271
InChiKey
IPBRDLJFHQZKFQ-UHFFFAOYSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

计算性质

  • 辛醇/水分配系数(LogP):
    3.5
  • 重原子数:
    16
  • 可旋转键数:
    2
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    58.4
  • 氢给体数:
    0
  • 氢受体数:
    3

反应信息

  • 作为产物:
    描述:
    5-溴-2-呋喃甲醛苯并噻吩-2-硼酸 在 palladium diacetate 四丁基溴化铵potassium carbonate 作用下, 以 为溶剂, 反应 2.0h, 以61%的产率得到5-(1-Benzothiophen-2-yl)furan-2-carbaldehyde
    参考文献:
    名称:
    Preparation of 5-Aryl Furfurals and Aryl Thiophene-2-carboxaldehydes via Palladium-Catalyzed C−C Bond Formation in Aqueous Media1
    摘要:
    [GRAPHICS]A series of 5-aryl furfurals and aryl thiophene-2-carboxaldehydes was synthesized. To this end, efficient and effective palladium-catalyzed C-C bond-forming reactions were carried out at room temperature in aqueous media. This mild process allowed the cross-coupling reaction of the bromides to occur in the presence of electrophilic functional groups, which is a valuable advantage over previously reported methods.
    DOI:
    10.1021/ol990708m
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文献信息

  • Thrombopoietin mimetics
    申请人:——
    公开号:US20030083361A1
    公开(公告)日:2003-05-01
    Invented are non-peptide TPO mimetics. Also invented is a method of treating thrombocytopenia, in a mammal, including a human, in need thereof which comprises administering to such mammal an effective amount of a selected substituted naphthimidazole derivative.
    发明了非肽类TPO类似物。还发明了一种治疗血小板减少症的方法,包括在需要的哺乳动物,包括人类中,向该哺乳动物施用所选取代咪唑生物的有效量。
  • CYANOTRIAZOLE COMPOUNDS
    申请人:OTSUKA PHARMACEUTICAL CO., LTD.
    公开号:US20160229816A1
    公开(公告)日:2016-08-11
    This invention relates to a cyanotriazole compound represented by the formula (1): wherein each symbols are defined in the specification, or a salt thereof. The compound or a salt thereof stimulates the citric acid cycle activity and/or improves hyperglycemia with less side effects, and excellent safety, and therefore, it is useful for treating and/or preventing diseases or disorders on which citric acid cycle activation and/or improvement of hyperglycemia has a prophylactic and/or therapeutic effect, for example, diabetes, impaired glucose tolerance, insulin resistance, diabetic complications, obesity, dyslipidemia, hepatic steatosis, atherosclerosis and/or cardiovascular disease, as well as diseases or disorders that would benefit from stimulating energy expenditure.
    本发明涉及一种由式(1)表示的基三唑化合物,其中每个符号在规范中有定义,或其盐。该化合物或其盐刺激柠檬酸循环活性和/或改善高血糖症的副作用较小,安全性优异,因此,它对于治疗和/或预防柠檬酸循环激活和/或改善高血糖症具有预防和/或治疗作用的疾病或疾病具有用处,例如糖尿病、糖耐量受损、胰岛素抵抗、糖尿病并发症、肥胖症、血脂异常、脂肪肝、动脉粥样硬化和/或心血管疾病,以及那些从刺激能量消耗中受益的疾病或疾病。
  • Mono and Dinuclear Palladium Pincer Complexes of NNSe Ligand as a Catalyst for Decarboxylative Direct C−H Heteroarylation of (Hetero)arenes
    作者:Sohan Singh、Vikki N. Shinde、Sunil Kumar、Neha Meena、Nattamai Bhuvanesh、Krishnan Rangan、Anil Kumar、Hemant Joshi
    DOI:10.1002/asia.202300628
    日期:2023.10.4
    NNSe pincer ligand and its palladium pincer complexes. Surprisingly, the reactivity of the ligand toward the palladium precursor is base-dependent. In the presence of the Et3N base, a mononuclear pincer complex was formed whereas in the absence of a base, a dinuclear pincer complex was formed. The complexes were used as catalysts for decarboxylative direct C−H heteroarylation of (hetero)arenes. Among
    本报告描述了新型 NNSe 钳形配体及其钳形配合物的合成。令人惊讶的是,配体前体的反应性是碱依赖性的。在存在Et 3 N碱基的情况下,形成单核钳复合物,而在不存在碱基的情况下,形成双核钳复合物。该配合物用作(杂)芳烃脱羧直接 C−H 杂芳基化的催化剂。在这些配合物中,发现双核配合物更具反应性。只需 2.5 mol% 的催化剂负载即可激活广泛的底物范围。
  • Cyanotriazole compounds
    申请人:OTSUKA PHARMACEUTICAL CO., LTD.
    公开号:US10626095B2
    公开(公告)日:2020-04-21
    This invention relates to a cyanotriazole compound represented by the formula (1): wherein each symbols are defined in the specification, or a salt thereof. The compound or a salt thereof stimulates the citric acid cycle activity and/or improves hyperglycemia with less side effects, and excellent safety, and therefore, it is useful for treating and/or preventing diseases or disorders on which citric acid cycle activation and/or improvement of hyperglycemia has a prophylactic and/or therapeutic effect, for example, diabetes, impaired glucose tolerance, insulin resistance, diabetic complications, obesity, dyslipidemia, hepatic steatosis, atherosclerosis and/or cardiovascular disease, as well as diseases or disorders that would benefit from stimulating energy expenditure.
    本发明涉及一种由式(1)表示的三唑化合物: 其中各符号在说明书中定义,或其盐。该化合物或其盐可刺激柠檬酸循环活性和/或改善高血糖,且副作用小、安全性高,因此可用于治疗和/或预防柠檬酸循环激活和/或改善高血糖具有预防和/或治疗作用的疾病或紊乱、例如,糖尿病、糖耐量受损、胰岛素抵抗、糖尿病并发症、肥胖症、血脂异常、肝脂肪变性、动脉粥样硬化和/或心血管疾病,以及可从刺激能量消耗中获益的疾病或紊乱。
  • THROMBOPOIETIN MIMETICS
    申请人:SmithKline Beecham Corporation
    公开号:EP1244446A1
    公开(公告)日:2002-10-02
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