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-methyl-2-phenyl-5-(4-trifluoromethylphenyl)-1H-imidazole | 1278587-21-5

中文名称
——
中文别名
——
英文名称
1-methyl-2-phenyl-5-(4-trifluoromethylphenyl)-1H-imidazole
英文别名
1-Methyl-2-phenyl-5-[4-(trifluoromethyl)phenyl]imidazole
1-methyl-2-phenyl-5-(4-trifluoromethylphenyl)-1H-imidazole化学式
CAS
1278587-21-5
化学式
C17H13F3N2
mdl
——
分子量
302.299
InChiKey
JJFQIKPCVBPJKJ-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:
    172-173 °C
  • 沸点:
    422.2±55.0 °C(Predicted)
  • 密度:
    1.21±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    4.2
  • 重原子数:
    22
  • 可旋转键数:
    2
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.12
  • 拓扑面积:
    17.8
  • 氢给体数:
    0
  • 氢受体数:
    4

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量
  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    4-碘苯甲醚1-methyl-2-phenyl-5-(4-trifluoromethylphenyl)-1H-imidazole 在 [Pd(phen)2](PF6)2 、 caesium carbonate 作用下, 以 N,N-二甲基乙酰胺 为溶剂, 反应 20.0h, 以36%的产率得到4-(4-methoxyphenyl)-N-methyl-2-phenyl-5-(4-trifluoromethylphenyl)imidazole
    参考文献:
    名称:
    One-pot Sequential Direct C–H Bond Arylation of Azoles Catalyzed by [Pd(phen)2](PF6)2: Synthetic Methods for Triarylated Azoles
    摘要:
    Synthetic methods for triarylated azoles containing three different aryl groups via one-pot sequential multiple C-H bond arylations are described. The one-pot sequential diarylation of C5-monoarylated azoles was achieved by the simple sequential addition of two different aryl iodides with a [Pd(phen)(2)]PF6 catalytic system. The one-pot triarylation of N-methylimidazole was achieved by the combination of a previously reported Pd(OAc)(2)-P(2-furyl)(3) system and the present [Pd(phen)(2)]PF6 system. In this case, portionwise addition of aryl halide, base and the catalyst in the final step significantly improved the overall yield of the desired triarylated product These protocols led to triarylated azoles without a loss of efficiency compared to the corresponding previously reported stepwise syntheses via direct C-H bond arylation.
    DOI:
    10.1021/jo301621t
  • 作为产物:
    描述:
    对溴三氟甲苯三(2-呋喃基)膦 、 [Pd(phen)2](PF6)2 、 palladium diacetate 、 potassium carbonatecaesium carbonate 作用下, 以 N,N-二甲基乙酰胺 为溶剂, 生成 1-methyl-2-phenyl-5-(4-trifluoromethylphenyl)-1H-imidazole
    参考文献:
    名称:
    One-pot Sequential Direct C–H Bond Arylation of Azoles Catalyzed by [Pd(phen)2](PF6)2: Synthetic Methods for Triarylated Azoles
    摘要:
    Synthetic methods for triarylated azoles containing three different aryl groups via one-pot sequential multiple C-H bond arylations are described. The one-pot sequential diarylation of C5-monoarylated azoles was achieved by the simple sequential addition of two different aryl iodides with a [Pd(phen)(2)]PF6 catalytic system. The one-pot triarylation of N-methylimidazole was achieved by the combination of a previously reported Pd(OAc)(2)-P(2-furyl)(3) system and the present [Pd(phen)(2)]PF6 system. In this case, portionwise addition of aryl halide, base and the catalyst in the final step significantly improved the overall yield of the desired triarylated product These protocols led to triarylated azoles without a loss of efficiency compared to the corresponding previously reported stepwise syntheses via direct C-H bond arylation.
    DOI:
    10.1021/jo301621t
点击查看最新优质反应信息

文献信息

  • C–H arylation and alkenylation of imidazoles by nickel catalysis: solvent-accelerated imidazole C–H activation
    作者:Kei Muto、Taito Hatakeyama、Junichiro Yamaguchi、Kenichiro Itami
    DOI:10.1039/c5sc02942b
    日期:——

    The first nickel-catalyzed C–H arylations and alkenylations of imidazoles with phenol and enol derivatives are described.

    第一个镍催化的咪唑与酚和烯醇衍生物的C-H芳基化和烯基化反应被描述了。
  • Direct Arylation of Simple Azoles Catalyzed by 1,10-Phenanthroline Containing Palladium Complexes: An Investigation of C4 Arylation of Azoles and the Synthesis of Triarylated Azoles by Sequential Arylation
    作者:Fumitoshi Shibahara、Eiji Yamaguchi、Toshiaki Murai
    DOI:10.1021/jo200067y
    日期:2011.4.15
    amounts of azoles, selective C5 monoarylation was achieved by using the same catalytic system. Subsequent efforts demonstrated that C5 arylated azoles undergo exclusive C2 arylation using [Pd(phen)2]PF6 as the catalyst with galvinoxyl as an additive. Finally, unprecedented C4 arylation reactions of 2,5-diaryl-azoles occur by using the new catalytic system to give the corresponding triarylated products in
    描述了由[Pd(phen)2 ] PF 6催化的简单唑的直接三芳基化和顺序三芳基化反应。在[Pd(phen)2 ] PF 6作为催化剂和化学计量的存在下,当使用芳基碘化物处理时,即使是简单的唑类,例如N-甲基咪唑,噻唑和恶唑,即使在其C4位上也发生三芳基化反应。150°C下DMA中Cs 2 CO 3的摩尔数。使用过量的唑类,使用相同的催化系统可实现选择性的C5单芳基化。随后的研究表明,C5芳基化的吡咯使用[Pd(phen)2 ] PF 6进行排他的C2芳基化作为催化剂,加尔维诺尔为添加剂。最后,通过使用新的催化体系,发生了前所未有的2,5-二芳基-唑的C4芳基化反应,从而以良好或优异的收率得到了相应的三芳基化产物。机理研究的结果表明,芳基化C2过程由电芳族取代(S的方式发生ë AR)palladation通路,而在C4位的芳基化反应经由A S发生ë氩palladation和/或自由基机理。
  • One-pot Sequential Direct C–H Bond Arylation of Azoles Catalyzed by [Pd(phen)<sub>2</sub>](PF<sub>6</sub>)<sub>2</sub>: Synthetic Methods for Triarylated Azoles
    作者:Fumitoshi Shibahara、Takayuki Yamauchi、Eiji Yamaguchi、Toshiaki Murai
    DOI:10.1021/jo301621t
    日期:2012.10.5
    Synthetic methods for triarylated azoles containing three different aryl groups via one-pot sequential multiple C-H bond arylations are described. The one-pot sequential diarylation of C5-monoarylated azoles was achieved by the simple sequential addition of two different aryl iodides with a [Pd(phen)(2)]PF6 catalytic system. The one-pot triarylation of N-methylimidazole was achieved by the combination of a previously reported Pd(OAc)(2)-P(2-furyl)(3) system and the present [Pd(phen)(2)]PF6 system. In this case, portionwise addition of aryl halide, base and the catalyst in the final step significantly improved the overall yield of the desired triarylated product These protocols led to triarylated azoles without a loss of efficiency compared to the corresponding previously reported stepwise syntheses via direct C-H bond arylation.
查看更多

同类化合物

伊莫拉明 (5aS,6R,9S,9aR)-5a,6,7,8,9,9a-六氢-6,11,11-三甲基-2-(2,3,4,5,6-五氟苯基)-6,9-甲基-4H-[1,2,4]三唑[3,4-c][1,4]苯并恶嗪四氟硼酸酯 (5-氨基-1,3,4-噻二唑-2-基)甲醇 齐墩果-2,12-二烯[2,3-d]异恶唑-28-酸 黄曲霉毒素H1 高效液相卡套柱 非昔硝唑 非布索坦杂质Z19 非布索坦杂质T 非布索坦杂质K 非布索坦杂质E 非布索坦杂质67 非布索坦杂质65 非布索坦杂质64 非布索坦杂质61 非布索坦代谢物67M-4 非布索坦代谢物67M-2 非布索坦代谢物 67M-1 非布索坦-D9 非布索坦 非唑拉明 雷西纳德杂质H 雷西纳德 阿西司特 阿莫奈韦 阿米苯唑 阿米特罗13C2,15N2 阿瑞匹坦杂质 阿格列扎 阿扎司特 阿尔吡登 阿塔鲁伦中间体 阿培利司N-1 阿哌沙班杂质26 阿哌沙班杂质15 阿可替尼 阿作莫兰 阿佐塞米 镁(2+)(Z)-4'-羟基-3'-甲氧基肉桂酸酯 锌1,2-二甲基咪唑二氯化物 铵2-(4-氯苯基)苯并恶唑-5-丙酸盐 铬酸钠[-氯-3-[(5-二氢-3-甲基-5-氧代-1-苯基-1H-吡唑-4-基)偶氮]-2-羟基苯磺酸基][4-[(3,5-二氯-2-羟基苯 铁(2+)乙二酸酯-3-甲氧基苯胺(1:1:2) 钠5-苯基-4,5-二氢吡唑-1-羧酸酯 钠3-[2-(2-壬基-4,5-二氢-1H-咪唑-1-基)乙氧基]丙酸酯 钠3-(2H-苯并三唑-2-基)-5-仲-丁基-4-羟基苯磺酸酯 钠(2R,4aR,6R,7R,7aS)-6-(2-溴-9-氧代-6-苯基-4,9-二氢-3H-咪唑并[1,2-a]嘌呤-3-基)-7-羟基四氢-4H-呋喃并[3,2-D][1,3,2]二氧杂环己膦烷e-2-硫醇2-氧化物 野麦枯 野燕枯 醋甲唑胺