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

N-(4-methylphenyl)-4-phenylbutanamide | 6876-67-1

中文名称
——
中文别名
——
英文名称
N-(4-methylphenyl)-4-phenylbutanamide
英文别名
——
N-(4-methylphenyl)-4-phenylbutanamide化学式
CAS
6876-67-1
化学式
C17H19NO
mdl
——
分子量
253.344
InChiKey
YDYWJEYZYHPIMX-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):
    3.7
  • 重原子数:
    19
  • 可旋转键数:
    5
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.24
  • 拓扑面积:
    29.1
  • 氢给体数:
    1
  • 氢受体数:
    1

反应信息

  • 作为产物:
    描述:
    N,N-diethyl-4-phenylbutanamide乙烷,三氯氟-三甲基氯硅烷1,10-菲罗啉六氯化钨 作用下, 以 N-甲基吡咯烷酮 为溶剂, 反应 36.0h, 以82%的产率得到N-(4-methylphenyl)-4-phenylbutanamide
    参考文献:
    名称:
    钨催化的叔烷基酰胺的转酰胺
    摘要:
    转酰胺最近已成为使酰胺多样化的一种简单方便的方法。然而,臭名昭著的、完全烷基取代的叔酰胺的动力学和热力学要求的转酰胺化仍然是一个长期的挑战。在这里,我们描述了一种使用简单的氯化钨 (VI) 作为催化剂和三甲基氯硅烷作为添加剂来活化叔烷基酰胺以简化转酰胺化的方法。高度亲电和亲氧的钨催化剂能够选择性地切断叔烷基酰胺的 C-N 键,从而实现无数结构和电子不同的叔烷基酰胺和胺的转酰胺化。
    DOI:
    10.1021/acscatal.1c01840
点击查看最新优质反应信息

文献信息

  • c-MET MODULATORS AND METHOD OF USE
    申请人:BANNEN CANNE LYNNE
    公开号:US20070244116A1
    公开(公告)日:2007-10-18
    The present invention provides compounds for modulating protein kinase enzymatic activity for modulating cellular activities such as proliferation, differentiation, programmed cell death, migration and chemoinvasion. More specifically, the invention provides quinazolines and quinolines which inhibit, regulate, and/or modulate kinase receptor, particularly c-Met, KDF, c-Kit, flt-3 and flt-4, signal transduction pathways related to the changes in cellular activities as mentioned above, compositions which contain these compounds, and methods of using them to treat kinase-dependent diseases and conditions. The present invention also provides methods for making compounds as mentioned above, and compositions which contain these compounds.
    本发明提供了用于调节蛋白激酶酶活性,以调节细胞活动,如增殖、分化、程序性细胞死亡、迁移和化学侵袭的化合物。更具体地,本发明提供了喹唑啉和喹啉,这些化合物抑制、调节和/或调节激酶受体,特别是c-Met、KDF、c-Kit、flt-3和flt-4,与上述细胞活动变化相关的信号转导途径,包含这些化合物的组合物,以及使用它们治疗激酶依赖性疾病和病况的方法。本发明还提供制备上述化合物的方法和包含这些化合物的组合物。
  • C-MET MODULATORS AND METHOD OF USE
    申请人:Bannen Canne Lynne
    公开号:US20070225307A1
    公开(公告)日:2007-09-27
    The present invention provides compounds for modulating protein kinase enzymatic activity for modulating cellular activities such as proliferation, differentiation, programmed cell death, migration and chemoinvasion. More specifically, the invention provides quinazolines and quinolines which inhibit, regulate, and/or modulate kinase receptor, particularly c-Met, KDF, c-Kit, flt-3 and flt-4, signal transduction pathways related to the changes in cellular activities as mentioned above, compositions which contain these compounds, and methods of using them to treat kinase-dependent diseases and conditions. The present invention also provides methods for making compounds as mentioned above, and compositions which contain these compounds.
    本发明提供了用于调节蛋白激酶酶活性以调节细胞活动(如增殖、分化、程序性细胞死亡、迁移和化学入侵)的化合物。更具体地,该发明提供了喹唑啉和喹啉,它们能够抑制、调节和/或调节激酶受体,特别是c-Met、KDF、c-Kit、flt-3和flt-4,与上述细胞活动变化相关的信号转导途径,包含这些化合物的组合物,以及使用它们治疗激酶依赖性疾病和病况的方法。本发明还提供了制备上述化合物和包含这些化合物的组合物的方法。
  • c-Met modulators and methods of use
    申请人:Bannen Canne Lynne
    公开号:US20070054928A1
    公开(公告)日:2007-03-08
    The present invention provides compounds for modulating protein kinase enzymatic activity for modulating cellular activities such as proliferation, differentiation, programmed cell death, migration and chemoinvasion. More specifically, the invention provides quinazolines and quinolines which inhibit, regulate and/or modulate kinase receptor, particularly c-Met, KDR, c-Kit, flt-3 and flt-4, signal transduction pathways related to the changes in cellular activities as mentioned above, compositions which contain these compounds, and methods of using them to treat kinase-dependent diseases and conditions. The present invention also provides methods for making compounds as mentioned above, and compositions which contain these compounds.
    本发明提供了用于调节蛋白激酶酶活性以调节细胞活动(如增殖、分化、程序性细胞死亡、迁移和化学入侵)的化合物。更具体地,本发明提供了能够抑制、调节和/或调节激酶受体,特别是c-Met、KDR、c-Kit、flt-3和flt-4,与上述细胞活动变化相关的信号转导途径的喹唑啉和喹啉,以及包含这些化合物的组合物和使用它们治疗激酶依赖性疾病和病况的方法。本发明还提供了制备上述化合物和包含这些化合物的组合物的方法。
  • C-Met Modulators and Methods of Use
    申请人:Forsyth Timothy Patrick
    公开号:US20080161305A1
    公开(公告)日:2008-07-03
    The present invention provides compounds, which have activity for modulating protein kinase enzymatic activity and are potentially useful for modulating cellular activities such as, e.g., proliferation, differentiation, programmed cell death, migration and chemoinvasion. The present invention also provides compositions containing such compounds, and methods for producing and using such compounds and compositions.
    本发明提供了一些化合物,这些化合物具有调节蛋白激酶酶活性的活性,并且可能有用于调节细胞活动,例如增殖、分化、程序性细胞死亡、迁移和化学侵袭等。本发明还提供了含有这些化合物的组合物,以及制备和使用这些化合物和组合物的方法。
  • c-MET MODULATORS AND METHODS OF USE
    申请人:BANNEN LYNNE CANNE
    公开号:US20090105299A1
    公开(公告)日:2009-04-23
    The present invention provides compounds for modulating protein kinase enzymatic activity for modulating cellular activities such as proliferation, differentiation, programmed cell death, migration and chemoinvasion. More specifically, the invention provides quinazolines and quinolines which inhibit, regulate, and/or modulate kinase receptor, particularly c-Met, KDF, c-Kit, flt-3 and flt-4, signal transduction pathways related to the changes in cellular activities as mentioned above, compositions which contain these compounds, and methods of using them to treat kinase-dependent diseases and conditions. The present invention also provides methods for making compounds as mentioned above, and compositions which contain these compounds.
    本发明提供了一种用于调节蛋白激酶酶活性,以调节细胞活动,如增殖、分化、程序性细胞死亡、迁移和化学侵袭的化合物。更具体地,本发明提供了喹唑啉和喹啉,它们抑制、调节和/或调节激酶受体,特别是c-Met、KDF、c-Kit、flt-3和flt-4,与上述细胞活动变化相关的信号转导通路,包含这些化合物的组合物,以及使用它们治疗激酶依赖性疾病和病况的方法。本发明还提供了制备上述化合物的方法和包含这些化合物的组合物。
查看更多

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