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2-[(2-ethyl)phenylamino]pyridine | 227805-83-6

中文名称
——
中文别名
——
英文名称
2-[(2-ethyl)phenylamino]pyridine
英文别名
N-2-pyridyl-2-ethylaniline;N-(2-ethylphenyl)pyridin-2-amine
2-[(2-ethyl)phenylamino]pyridine化学式
CAS
227805-83-6
化学式
C13H14N2
mdl
MFCD24389996
分子量
198.268
InChiKey
BTBDKDGNZZWUFT-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:
    15
  • 可旋转键数:
    3
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.153
  • 拓扑面积:
    24.9
  • 氢给体数:
    1
  • 氢受体数:
    2

反应信息

  • 作为反应物:
    描述:
    2-[(2-ethyl)phenylamino]pyridine四氯化钛 在 sodium hydride 作用下, 以 乙醚甲苯 为溶剂, 生成 bis(2-(2-ethyl)phenylaminopyridinato) titanium dichloridecomplex
    参考文献:
    名称:
    双(烷基苯基氨基吡啶并)二氯化钛作为乙烯聚合催化剂
    摘要:
    衍生自2-(2-乙基苯胺基)-,2-(3,5-二甲基苯胺基)吡啶,2-(4-正丁基苯胺基)-和2-(2- t合成了丁基丁基苯胺基吡啶并通过光谱法对其进行了表征。在MAO作为助催化剂的存在下,这些络合物用于催化乙烯的聚合。研究了复杂结构对聚合行为的影响。本研究中使用的所有烷基苯基氨基吡啶并钛配合物比未取代的双(苯基氨基吡啶并)二氯化钛配合物具有更高的摩尔质量。相应地,与未取代的双(苯基氨基吡啶并)钛催化剂相比,活性较低,摩尔质量分布较宽。烷基苯基氨基吡啶基钛催化剂的流动行为可能是摩尔质量分布较宽的原因。
    DOI:
    10.1016/j.molcata.2007.10.029
  • 作为产物:
    描述:
    2-溴吡啶2-乙基苯胺 在 、 sodium t-butanolate 作用下, 以 甲苯 为溶剂, 反应 22.0h, 生成 2-[(2-ethyl)phenylamino]pyridine
    参考文献:
    名称:
    Efficient catalytic aryl amination of bromoarenes using 3-iminophosphine palladium(II) chloride
    摘要:
    While pursuing the development of new hydroamination catalysts, a 3-iminophosphine palladium(II) chloride complex [(3IP)PdCl2] was synthesized that has subsequently proven to be an effective precatalyst for the aryl amination of bromoarenes. This (3IP)PdCl2 complex has been utilized in the catalytic aryl amination of both bromobenzene and bromopyridine derivatives, specifically yielding excellent activity in coupling reactions involving bromobenzene, 4-bromotoluene, and 2-bromopyridine. Using a standard set of catalytic conditions, many alkyl and aryl amines have been investigated as coupling partners in the aryl amination of bromoarenes. In general, secondary alkyl amines and ortho-substituted anilines proved to be the best substrates for this reaction, commonly giving quantitative conversion to products, while primary amines and other anilines gave only poor to moderate results. Catalytic screening data, product yields, and full characterization of isolated products are included. (C) 2012 Elsevier B.V. All rights reserved.
    DOI:
    10.1016/j.jorganchem.2012.08.027
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文献信息

  • Rhodium-Catalyzed Synthesis of 2-Methylindoles via C–N Bond Cleavage of <i>N</i>-Allylbenzimidazole
    作者:Pragati Biswal、Tanmayee Nanda、Namrata Prusty、Smruti Ranjan Mohanty、Ponneri C. Ravikumar
    DOI:10.1021/acs.joc.2c03048
    日期:2023.7.7
    A rhodium-catalyzed oxidative C–H/N–H dehydrogenative [3 + 2] annulation strategy has been reported between anilines and N-allylbenzimidazole for the synthesis of 2-methylindole scaffolds. An N-allylbenzimidazole has been used as a 2C synthon for the synthesis of indole, and more importantly, this transformation involves the cleavage of the thermodynamically stable C–N bond of allylamine. Detailed
    据报道,苯胺和N-烯丙基苯并咪唑之间存在铑催化的氧化 C-H/N-H 脱氢 [3 + 2] 成环策略,用于合成 2-甲基吲哚支架。N-烯丙基苯并咪唑已被用作合成吲哚的2C合成子,更重要的是,这种转化涉及烯丙胺热力学稳定的C-N键的断裂。详细的机理研究已经完成,并在 HRMS 中检测到了关键的中间体。这种转化通过 C(sp 2 )–H 烯丙基化级联和随后的分子内环化进行。
  • 3-PIPERIDYL-4-OXOQUINAZOLINE DERIVATIVES AND MEDICINCAL COMPOSITIONS CONTAINING THE SAME
    申请人:Japan Tobacco Inc.
    公开号:EP0970954A1
    公开(公告)日:2000-01-12
    3-piperidyl-4-oxoquinazoline derivatives are provided, which is represented by the formula (I): wherein R represents an amino group or a cyclic amino group such as dibenzoazepine, each of which is substituted with a substituted or unsubstituted aryl group, a substituted or unsubstituted heteroaryl group, or the like, n is an integer of 1 to 4, R3 and R4 independently represents a hydrogen atom, a lower alkyl group, or the like, or a pharmaceutically acceptable salt thereof. Compounds (I) of the present invention have excellent MTP-inhibitory activity. Thus, these compounds not only inhibit formation of LDL that is a cause of arteriosclerotic diseases but also regulate TG, cholesterol, and lipoproteins such as LDL in the blood and regulate cellular lipids through regulation of MTP activity. They can also be used as a new type of preventive or therapeutic agents for hyperlipemia or arteriosclerotic diseases. Furthermore, they can be used as therapeutic or preventive agents for pancreatitis, obesity, hypercholesterolemia, and hypertriglyceridemia.
    提供了3-哌啶基-4-氧代喹唑啉衍生物,由式(I)表示: 其中 R 代表氨基或环状氨基,如二苯并氮杂卓,它们各自被取代或未被取代的芳基、取代或未被取代的杂芳基或类似基团取代,n 是 1 至 4 的整数,R3 和 R4 独立地代表氢原子、低级烷基或类似基团,或其药学上可接受的盐。本发明的化合物(I)具有优异的 MTP 抑制活性。因此,这些化合物不仅能抑制导致动脉硬化疾病的低密度脂蛋白的形成,还能调节血液中的总胆固醇、胆固醇和脂蛋白(如低密度脂蛋白),并通过调节 MTP 活性来调节细胞脂质。它们还可用作高脂血症或动脉硬化疾病的新型预防或治疗药物。此外,它们还可用作胰腺炎、肥胖症、高胆固醇血症和高甘油三酯血症的治疗或预防药物。
  • US6235730B1
    申请人:——
    公开号:US6235730B1
    公开(公告)日:2001-05-22
  • Efficient catalytic aryl amination of bromoarenes using 3-iminophosphine palladium(II) chloride
    作者:Danielle C. Samblanet、Joseph A.R. Schmidt
    DOI:10.1016/j.jorganchem.2012.08.027
    日期:2012.12
    While pursuing the development of new hydroamination catalysts, a 3-iminophosphine palladium(II) chloride complex [(3IP)PdCl2] was synthesized that has subsequently proven to be an effective precatalyst for the aryl amination of bromoarenes. This (3IP)PdCl2 complex has been utilized in the catalytic aryl amination of both bromobenzene and bromopyridine derivatives, specifically yielding excellent activity in coupling reactions involving bromobenzene, 4-bromotoluene, and 2-bromopyridine. Using a standard set of catalytic conditions, many alkyl and aryl amines have been investigated as coupling partners in the aryl amination of bromoarenes. In general, secondary alkyl amines and ortho-substituted anilines proved to be the best substrates for this reaction, commonly giving quantitative conversion to products, while primary amines and other anilines gave only poor to moderate results. Catalytic screening data, product yields, and full characterization of isolated products are included. (C) 2012 Elsevier B.V. All rights reserved.
  • Bis(alkylphenylaminopyridinato) titanium dichlorides as ethylene polymerization catalysts
    作者:Markku Talja、Mika Polamo、Markku Leskelä
    DOI:10.1016/j.molcata.2007.10.029
    日期:2008.2
    titanium complexes derived from 2-(2-ethylanilino)-, 2-(3,5-dimethylanilino)pyridine, 2-(4-n-butylanilino)- and 2-(2-t-butylanilino)pyridine were synthesized and characterized by spectroscopic methods. These complexes were used to catalyze the polymerization of ethylene in the presence of MAO as cocatalyst. The effect of the complex structures on the polymerization behavior was studied. All the alkylp
    衍生自2-(2-乙基苯胺基)-,2-(3,5-二甲基苯胺基)吡啶,2-(4-正丁基苯胺基)-和2-(2- t合成了丁基丁基苯胺基吡啶并通过光谱法对其进行了表征。在MAO作为助催化剂的存在下,这些络合物用于催化乙烯的聚合。研究了复杂结构对聚合行为的影响。本研究中使用的所有烷基苯基氨基吡啶并钛配合物比未取代的双(苯基氨基吡啶并)二氯化钛配合物具有更高的摩尔质量。相应地,与未取代的双(苯基氨基吡啶并)钛催化剂相比,活性较低,摩尔质量分布较宽。烷基苯基氨基吡啶基钛催化剂的流动行为可能是摩尔质量分布较宽的原因。
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同类化合物

(βS)-β-氨基-4-(4-羟基苯氧基)-3,5-二碘苯甲丙醇 (S)-(-)-7'-〔4(S)-(苄基)恶唑-2-基]-7-二(3,5-二-叔丁基苯基)膦基-2,2',3,3'-四氢-1,1-螺二氢茚 (S)-盐酸沙丁胺醇 (S)-3-(叔丁基)-4-(2,6-二甲氧基苯基)-2,3-二氢苯并[d][1,3]氧磷杂环戊二烯 (S)-2,2'-双[双(3,5-三氟甲基苯基)膦基]-4,4',6,6'-四甲氧基联苯 (S)-1-[3,5-双(三氟甲基)苯基]-3-[1-(二甲基氨基)-3-甲基丁烷-2-基]硫脲 (R)富马酸托特罗定 (R)-(-)-盐酸尼古地平 (R)-(+)-7-双(3,5-二叔丁基苯基)膦基7''-[((6-甲基吡啶-2-基甲基)氨基]-2,2'',3,3''-四氢-1,1''-螺双茚满 (R)-3-(叔丁基)-4-(2,6-二苯氧基苯基)-2,3-二氢苯并[d][1,3]氧杂磷杂环戊烯 (R)-2-[((二苯基膦基)甲基]吡咯烷 (N-(4-甲氧基苯基)-N-甲基-3-(1-哌啶基)丙-2-烯酰胺) (5-溴-2-羟基苯基)-4-氯苯甲酮 (5-溴-2-氯苯基)(4-羟基苯基)甲酮 (5-氧代-3-苯基-2,5-二氢-1,2,3,4-oxatriazol-3-鎓) (4S,5R)-4-甲基-5-苯基-1,2,3-氧代噻唑烷-2,2-二氧化物-3-羧酸叔丁酯 (4-溴苯基)-[2-氟-4-[6-[甲基(丙-2-烯基)氨基]己氧基]苯基]甲酮 (4-丁氧基苯甲基)三苯基溴化磷 (3aR,8aR)-(-)-4,4,8,8-四(3,5-二甲基苯基)四氢-2,2-二甲基-6-苯基-1,3-二氧戊环[4,5-e]二恶唑磷 (2Z)-3-[[(4-氯苯基)氨基]-2-氰基丙烯酸乙酯 (2S,3S,5S)-5-(叔丁氧基甲酰氨基)-2-(N-5-噻唑基-甲氧羰基)氨基-1,6-二苯基-3-羟基己烷 (2S,2''S,3S,3''S)-3,3''-二叔丁基-4,4''-双(2,6-二甲氧基苯基)-2,2'',3,3''-四氢-2,2''-联苯并[d][1,3]氧杂磷杂戊环 (2S)-(-)-2-{[[[[3,5-双(氟代甲基)苯基]氨基]硫代甲基]氨基}-N-(二苯基甲基)-N,3,3-三甲基丁酰胺 (2S)-2-[[[[[[((1R,2R)-2-氨基环己基]氨基]硫代甲基]氨基]-N-(二苯甲基)-N,3,3-三甲基丁酰胺 (2-硝基苯基)磷酸三酰胺 (2,6-二氯苯基)乙酰氯 (2,3-二甲氧基-5-甲基苯基)硼酸 (1S,2S,3S,5S)-5-叠氮基-3-(苯基甲氧基)-2-[(苯基甲氧基)甲基]环戊醇 (1-(4-氟苯基)环丙基)甲胺盐酸盐 (1-(3-溴苯基)环丁基)甲胺盐酸盐 (1-(2-氯苯基)环丁基)甲胺盐酸盐 (1-(2-氟苯基)环丙基)甲胺盐酸盐 (-)-去甲基西布曲明 龙胆酸钠 龙胆酸叔丁酯 龙胆酸 龙胆紫 龙胆紫 齐达帕胺 齐诺康唑 齐洛呋胺 齐墩果-12-烯[2,3-c][1,2,5]恶二唑-28-酸苯甲酯 齐培丙醇 齐咪苯 齐仑太尔 黑染料 黄酮,5-氨基-6-羟基-(5CI) 黄酮,6-氨基-3-羟基-(6CI) 黄蜡,合成物 黄草灵钾盐