摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

1-甲基-2-(2-噻吩基)吡咯烷 | 98960-71-5

中文名称
1-甲基-2-(2-噻吩基)吡咯烷
中文别名
——
英文名称
1-methyl-2-(2-thienyl)pyrrolidine
英文别名
1-Methyl-2--pyrrolidin;1-methyl-2-thiophen-2-yl-pyrrolidine;1-Methyl-2-[2]thienyl-pyrrolidin;1-methyl-2-thiophen-2-ylpyrrolidine
1-甲基-2-(2-噻吩基)吡咯烷化学式
CAS
98960-71-5
化学式
C9H13NS
mdl
——
分子量
167.275
InChiKey
AGGVOBMIIGKVIE-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

物化性质

  • 熔点:
    124-125 °C
  • 沸点:
    88-90 °C(Press: 2 Torr)
  • 密度:
    1.090±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    2
  • 重原子数:
    11
  • 可旋转键数:
    1
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.56
  • 拓扑面积:
    31.5
  • 氢给体数:
    0
  • 氢受体数:
    2

反应信息

  • 作为反应物:
    描述:
    1-甲基-2-(2-噻吩基)吡咯烷 、 sodium amide 作用下, 以 乙醚 为溶剂, 反应 24.0h, 生成 5-methyl-6,7,8,9-tetrahydro-4H-thieno[3,2-c]azocine
    参考文献:
    名称:
    Cotelle, Philippe; Hasiak, Bruno; Barby, Didier, Synthetic Communications, 1987, vol. 17, # 8, p. 935 - 942
    摘要:
    DOI:
  • 作为产物:
    描述:
    聚合甲醛 、 alkaline earth salt of/the/ methylsulfuric acid 在 甲酸 作用下, 生成 1-甲基-2-(2-噻吩基)吡咯烷
    参考文献:
    名称:
    Synthesis of Nicotine Analogs1
    摘要:
    DOI:
    10.1021/jo01103a012
点击查看最新优质反应信息

文献信息

  • [EN] AMIDO-THIOPHENE COMPOUNDS AND THEIR USE<br/>[FR] COMPOSÉS AMIDO-THIOPHÈNE ET LEUR UTILISATION
    申请人:UNIV EDINBURGH
    公开号:WO2009112845A1
    公开(公告)日:2009-09-17
    The present invention pertains generally to the field of therapeutic compounds. More specifically the present invention pertains to certain amido-thiophene compounds that, inter alia, inhibit 11 β-hydroxysteroid dehydrogenase type 1 (11 β-HSD1 ). The present invention also pertains to pharmaceutical compositions comprising such compounds, and the use of such compounds and compositions, both in vitro and in vivo, to inhibit 11 β-hydroxysteroid dehydrogenase type 1; to treat disorders that are ameliorated by the inhibition of 11 β-hydroxysteroid dehydrogenase type 1; to treat the metabolic syndrome, which includes disorders such as type 2 diabetes and obesity, and associated disorders including insulin resistance, hypertension, lipid disorders and cardiovascular disorders such as ischaemic (coronary) heart disease; to treat CNS disorders such as mild cognitive impairment and early dementia, including Alzheimer's disease; etc.
    本发明一般涉及治疗化合物领域。更具体地,本发明涉及某些酰胺-噻吩化合物,其中包括抑制11β-羟基类固醇脱氢酶1(11β-HSD1)的作用。本发明还涉及包含这些化合物的药物组合物,以及使用这些化合物和组合物,在体内和体外,抑制11β-羟基类固醇脱氢酶1;治疗通过抑制11β-羟基类固醇脱氢酶1而得到改善的疾病;治疗代谢综合征,其中包括糖尿病和肥胖等疾病,以及相关疾病,包括胰岛素抵抗、高血压、脂质紊乱和心血管疾病,如缺血性(冠状)心脏病;治疗中枢神经系统疾病,如轻度认知障碍和早期痴呆,包括阿尔茨海默病等。
  • COMPOUNDS FOR THE TREATMENT OF CANCER AND INFLAMMATORY DISEASE
    申请人:SHY Therapeutics LLC
    公开号:US20170174699A1
    公开(公告)日:2017-06-22
    Provided herein are compounds that inhibit the phosphorylation of MAPK and thus are useful in compositions and methods for treating cancer and inflammatory disease.
    本文提供了抑制MAPK磷酸化的化合物,因此可用于治疗癌症和炎症性疾病的组合物和方法。
  • Chemical Compounds
    申请人:Kerns K. Jeffrey
    公开号:US20070254873A1
    公开(公告)日:2007-11-01
    The invention is directed to novel indole carboxamide derivatives. Specifically, the invention is directed to compounds according to formula I: where R1, R2, R3, U and V are defined below and to pharmaceutically acceptable salts thereof. The compounds of the invention are inhibitors of IKK2 and can be useful in the treatment of disorders associated with inappropriate IKK2 (also known as IKKβ) activity, such as rheumatoid arthritis, asthma, and COPD (chronic obstructive pulmonary disease). Accordingly, the invention is further directed to pharmaceutical compositions comprising a compound of the invention. The invention is still further directed to methods of inhibiting IKK2 activity and treatment of disorders associated therewith using a compound of the invention or a pharmaceutical composition comprising a compound of the invention.
    本发明涉及新型吲哚羧酰胺衍生物。具体而言,本发明涉及公式I所示的化合物:其中R1,R2,R3,U和V如下所定义,及其药学上可接受的盐。本发明的化合物是IKK2的抑制剂,可用于治疗与不适当的IKK2(也称为IKKβ)活性有关的疾病,如类风湿性关节炎、哮喘和COPD(慢性阻塞性肺疾病)。因此,本发明还涉及包含本发明化合物的药物组合物。本发明还进一步涉及使用本发明化合物或包含本发明化合物的药物组合物来抑制IKK2活性和治疗与此相关的疾病的方法。
  • Amido-Isothiazole Compounds and Their Use as Inhibitors of 11Beta-HSD1 for the Treatment of Metabolic Syndrome and Related Disorders
    申请人:Webster Scott Peter
    公开号:US20120095046A1
    公开(公告)日:2012-04-19
    The present invention pertains generally to the field of therapeutic compounds. More specifically the present invention pertains to certain amido-isothiazole compounds that, inter alia, inhibit 11β-hydroxysteroid dehydrogenase type 1 (11β-HSD1). The present invention also pertains to pharmaceutical compositions comprising such compounds, and the use of such compounds and compositions, both in vitro and in vivo, to inhibit 11β-hydroxysteroid dehydrogenase type 1; to treat disorders that are ameliorated by the inhibition of 11β-hydroxysteroid dehydrogenase type 1; to treat the metabolic syndrome, which includes disorders such as type 2 diabetes and obesity, and associated disorders including insulin resistance, hypertension, lipid disorders and cardiovascular disorders such as ischaemic (coronary) heart disease; to treat CNS disorders such as mild cognitive impairment and early dementia, including Alzheimer's disease; etc.
    本发明一般涉及治疗化合物领域。更具体地,本发明涉及某些酰胺异噻唑化合物,其在其他方面抑制11β-羟基类固醇脱氢酶1型(11β-HSD1)。本发明还涉及包括这些化合物的制药组合物,并且在体内外使用这些化合物和组合物以抑制11β-羟基类固醇脱氢酶1型;治疗通过抑制11β-羟基类固醇脱氢酶1型改善的疾病;治疗代谢综合症,包括2型糖尿病和肥胖症,以及相关疾病,包括胰岛素抵抗、高血压、脂质代谢紊乱和缺血性(冠状动脉)心脏病等;治疗中枢神经系统疾病,如轻度认知障碍和早期痴呆,包括阿尔茨海默病等。
  • Amido-Thiophene Compounds and Their Use
    申请人:Webster Scott Peter
    公开号:US20130012545A1
    公开(公告)日:2013-01-10
    The present invention pertains generally to the field of therapeutic compounds. More specifically the present invention pertains to certain amido-thiophene compounds that, inter alia, inhibit 11β-hydroxysteroid dehydrogenase type 1 (11β-HSD1). The present invention also pertains to pharmaceutical compositions comprising such compounds, and the use of such compounds and compositions, both in vitro and in vivo, to inhibit 11β-hydroxysteroid dehydrogenase type 1; to treat disorders that are ameliorated by the inhibition of 11β-hydroxysteroid dehydrogenase type 1; to treat the metabolic syndrome, which includes disorders such as type 2 diabetes and obesity, and associated disorders including insulin resistance, hypertension, lipid disorders and cardiovascular disorders such as ischaemic (coronary) heart disease; to treat CNS disorders such as mild cognitive impairment and early dementia, including Alzheimer's disease; etc.
    本发明通常涉及治疗化合物领域。更具体地,本发明涉及某些酰胺噻吩化合物,其在其他方面抑制11β-羟化固醇脱氢酶1型(11β-HSD1)。本发明还涉及包括这些化合物的制药组合物,并且在体内外使用这些化合物和组合物来抑制11β-羟化固醇脱氢酶1型;治疗通过抑制11β-羟化固醇脱氢酶1型改善的疾病;治疗代谢综合征,包括2型糖尿病和肥胖症等疾病,以及相关疾病,包括胰岛素抵抗、高血压、脂质代谢紊乱和缺血性(冠状动脉)心脏病等心血管疾病;治疗CNS疾病,如轻度认知障碍和早期痴呆,包括阿尔茨海默病等。
查看更多

同类化合物

(N-(2-甲基丙-2-烯-1-基)乙烷-1,2-二胺) (4-(苄氧基)-2-(哌啶-1-基)吡啶咪丁-5-基)硼酸 (11-巯基十一烷基)-,,-三甲基溴化铵 鼠立死 鹿花菌素 鲸蜡醇硫酸酯DEA盐 鲸蜡硬脂基二甲基氯化铵 鲸蜡基胺氢氟酸盐 鲸蜡基二甲胺盐酸盐 高苯丙氨醇 高箱鲀毒素 高氯酸5-(二甲氨基)-1-({(E)-[4-(二甲氨基)苯基]甲亚基}氨基)-2-甲基吡啶正离子 高氯酸2-氯-1-({(E)-[4-(二甲氨基)苯基]甲亚基}氨基)-6-甲基吡啶正离子 高氯酸2-(丙烯酰基氧基)-N,N,N-三甲基乙铵 马诺地尔 马来酸氢十八烷酯 马来酸噻吗洛尔EP杂质C 马来酸噻吗洛尔 马来酸倍他司汀 顺式环己烷-1,3-二胺盐酸盐 顺式氯化锆二乙腈 顺式吡咯烷-3,4-二醇盐酸盐 顺式双(3-甲氧基丙腈)二氯铂(II) 顺式3,4-二氟吡咯烷盐酸盐 顺式1-甲基环丙烷1,2-二腈 顺式-二氯-反式-二乙酸-氨-环己胺合铂 顺式-二抗坏血酸(外消旋-1,2-二氨基环己烷)铂(II)水合物 顺式-N,2-二甲基环己胺 顺式-4-甲氧基-环己胺盐酸盐 顺式-4-环己烯-1.2-二胺 顺式-4-氨基-2,2,2-三氟乙酸环己酯 顺式-2-甲基环己胺 顺式-2-(苯基氨基)环己醇 顺式-2-(氨基甲基)-1-苯基环丙烷羧酸盐酸盐 顺式-1,3-二氨基环戊烷 顺式-1,2-环戊烷二胺 顺式-1,2-环丁腈 顺式-1,2-双氨甲基环己烷 顺式--N,N'-二甲基-1,2-环己二胺 顺式-(R,S)-1,2-二氨基环己烷铂硫酸盐 顺式-(2-氨基-环戊基)-甲醇 顺-2-戊烯腈 顺-1,3-环己烷二胺 顺-1,3-双(氨甲基)环己烷 顺,顺-丙二腈 非那唑啉 靛酚钠盐 靛酚 霜霉威盐酸盐 霜脲氰