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N1,N1-diethyl-3-methoxybenzene-1,4-diamine | 2165-85-7

中文名称
——
中文别名
——
英文名称
N1,N1-diethyl-3-methoxybenzene-1,4-diamine
英文别名
4-N,4-N-diethyl-2-methoxybenzene-1,4-diamine
N<sup>1</sup>,N<sup>1</sup>-diethyl-3-methoxybenzene-1,4-diamine化学式
CAS
2165-85-7
化学式
C11H18N2O
mdl
——
分子量
194.277
InChiKey
LGMWBTURBRPNCJ-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):
    2.1
  • 重原子数:
    14
  • 可旋转键数:
    4
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.45
  • 拓扑面积:
    38.5
  • 氢给体数:
    1
  • 氢受体数:
    3

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

反应信息

  • 作为反应物:
    描述:
    N1,N1-diethyl-3-methoxybenzene-1,4-diamine氯化铵三乙胺三氟乙酸 作用下, 以 四氢呋喃甲醇二氯甲烷仲丁醇 为溶剂, 反应 8.0h, 生成 N-(3-((5-chloro-2-((4-(diethylamino)-2-methoxyphenyl)amino)pyrimidin-4-yl)oxy)phenyl)propionamide
    参考文献:
    名称:
    Optimization of WZ4003 as NUAK inhibitors against human colorectal cancer
    摘要:
    DOI:
    10.1016/j.ejmech.2020.113080
  • 作为产物:
    描述:
    N,N-diethyl-3-methoxy-4-nitroaniline 在 palladium 10% on activated carbon 盐酸氢气 作用下, 以 甲醇 为溶剂, 反应 1.0h, 生成 N1,N1-diethyl-3-methoxybenzene-1,4-diamine
    参考文献:
    名称:
    Isoxazole carboxamide derivatives as ghrelin receptor modulators
    摘要:
    本发明涉及式(I)的化合物,或其在治疗上适用的盐或前药,该化合物的制备,含有该化合物的组合物以及在预防或治疗由胃饥素调节的疾病中使用该化合物,包括厌食症、癌症恶病质、进食障碍、与年龄相关的身体组成下降、体重增加、肥胖和糖尿病。
    公开号:
    US20060089398A1
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文献信息

  • Isoxazole carboxamide derivatives as ghrelin receptor modulators
    申请人:Liu Gang
    公开号:US20060089398A1
    公开(公告)日:2006-04-27
    The present invention is related to compounds of formula (I), or a therapeutically suitable salt or prodrug thereof, the preparation of the compounds, compositions containing the compounds and the use of the compounds in the prevention or treatment of disorders regulated by ghrelin including anorexia, cancer cachexia, eating disorders, age-related decline in body composition, weight gain, obesity, and diabetes mellitus.
    本发明涉及式(I)的化合物,或其在治疗上适用的盐或前药,该化合物的制备,含有该化合物的组合物以及在预防或治疗由胃饥素调节的疾病中使用该化合物,包括厌食症、癌症恶病质、进食障碍、与年龄相关的身体组成下降、体重增加、肥胖和糖尿病。
  • Discovery of N -aryl- N ′-pyrimidin-4-yl ureas as irreversible L858R/T790M mutant selective epidermal growth factor receptor inhibitors
    作者:Fusheng Zhou、Liang Zhang、Yunzhou Jin、Wei Liu、Pengfei Cheng、Xiangyu He、Jing Xie、Sida Shen、Jing Lei、Haixia Ji、Yi Hu、Yingtao Liu、Yumin Cui、Qiang Lv、Jiong Lan
    DOI:10.1016/j.bmcl.2017.12.009
    日期:2018.4
    series of N-aryl-N′-pyrimidin-4-yl ureas has been optimized to afford potent and selective inhibitors of the EGFR L858R/T790M. The most representative compound 28 showed high activity against EGFR L858R/T790M kinase (IC50 = 4 nM) and 22-fold selectivity against wild type EGFR. Moreover, compound 28 potently inhibited EGFR L858R/T790M phosphorylation (IC50 = 41 nM) and cellular proliferation (IC50 = 37 nM)
    已经优化了一系列新的N-芳基-N'-嘧啶-4-基脲,以提供有效的和选择性的EGFR L858R / T790M抑制剂。最有代表性的化合物28对EGFR L858R / T790M激酶显示高活性(IC 50  = 4 nM),对野生型EGFR的选择性是22倍。此外,化合物28 在H1975细胞系中有效抑制EGFR L858R / T790M磷酸化(IC 50  = 41 nM)和细胞增殖(IC 50 = 37 nM),同时对A431细胞的毒性明显降低。此外,化合物28在激酶的小面板中显示出很大的选择性。
  • Photographic colour couplers and light-sensitive material containing them
    申请人:FUJI PHOTO FILM CO., LTD.
    公开号:EP0024033A1
    公开(公告)日:1981-02-18
    A silver halide photographic light-sensitive material containing a colorless photographic cyan color forming coupler having, in a position for coupling with an oxidation product of an aromatic primary amine developing agent, a coupling-off arouD reDresented by the formula (I): wherein R represents a substituted alkylene group or an unsubstituted or substituted alkenylene group, and said alkylene group or alkenylene group may be straight or branched chain; and R represents a substituted or unsubstituted alkyl group, an alkenyl group, an aralkyl group, an aralkenyl group, a cycloalkyl group or a heterocyclic group and said alkyl group, alkenyl group, aralkyl group and aralkenyl group may be straight or branched chain; and said heterocyclic group being connected with a thio group at the position of a carbon atom of the heterocyclic group.
    一种含有无色照相青色形成耦合剂的卤化银感光材料,该耦合剂在与芳香族伯胺显影剂的氧化产物耦合的位置上具有由式(I)表示的耦合断裂: 其中 R 代表取代的亚烷基或未取代或取代的烯基,所述亚烷基或烯基可以是直链或支链;R 代表取代或未取代的烷基、烯基、芳基、芳烯基、环烷基或杂环基,且所述烷基、烯基、芳基和芳烯基可以是直链或支链;且所述杂环基在杂环基碳原子的位置上与硫代基团相连。
  • Novel quinazoline-dione compounds, process for production thereof and pharmaceutical use thereof
    申请人:Ishikawa, Masayuki
    公开号:EP0040793A1
    公开(公告)日:1981-12-02
    A 5,6,7-substituted-2,4 (1H,3H)-quinazolinedione compound of the formula (I), wherein R1, R2, R3, A and B as defined in claim 1 and its acid addition salt; and a vasodilating and hypotensive composition containing the aforesaid compound.
    一种式(I)的 5,6,7-取代的-2,4(1H,3H)-喹唑啉二酮化合物、 其中 R1、R2、R3、A 和 B 如权利要求 1 所定义及其酸加成盐;以及含有上述化合物的血管扩张和降血压组合物。
  • Method for preventing an organic colored substance from fading by light, stabilized colored compositions and photographic elements and materials
    申请人:KONICA CORPORATION
    公开号:EP0286850A1
    公开(公告)日:1988-10-19
    A method for preventing organic colored substance from fading by light comprising, adding to said organic colored substance a compound of the formula (I) wherein R is a substituent and n is an integer from 0 to 6, provided that when n is 2 or higher. the R's may be either the same or different from each other and they may be combined with each other to form a ring. Stabilized colored compositions and photographic elements and materials containing the compounds of formula (I).
    一种防止有机有色物质在光照下褪色的方法,包括: 在所述有机有色物质中加入式(I)化合物,其中 R 是取代基,n 是 0 至 6 的整数。 其中 R 是取代基,n 是 0-6 之间的整数,但当 n 为 2 或更大时,R 可以相同或不同,并且可以相互结合形成一个环。含有式 (I) 化合物的稳定彩色组合物、照相元件和材料。
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