N-((1H-benzo[d][1,2,3]triazole)-1-methyl)-4-cyanoaniline

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 苯并三唑类
• 英文名称: N-((1H-benzo[d][1,2,3]triazole)-1-methyl)-4-cyanoaniline
• 英文别名: 4-[(1H-1,2,3-Benzotriazol-1-ylmethyl)amino]benzonitrile；4-(benzotriazol-1-ylmethylamino)benzonitrile
• 化学式: C₁₄H₁₁N₅
• 分子量: 249.275
• InChiKey: VKRLPAIOEFEHJN-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.7
• 重原子数：
  19
• 可旋转键数：
  3
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.07
• 拓扑面积：
  66.5
• 氢给体数：
  1
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  溴甲苯 、 N-((1H-benzo[d][1,2,3]triazole)-1-methyl)-4-cyanoaniline 在 锌 作用下， 以 四氢呋喃 为溶剂， 反应 12.0h， 以56%的产率得到4-(phenethylamino)benzonitrile
  参考文献：
  名称：

  The preparation of functionalized amines and amides using benzotriazole derivatives and organozinc reagents

  摘要：

  Secondary and tertiary amines 6 are conveniently prepared in good yields by reacting organozinc halides with adducts 4, which are derived from the corresponding amines, aldehydes and benzotriazole. The use of organozinc reagents enables the introduction of nitro, cyano or ester functionalities into amine mainframes. This methodology was also used to prepare functionalized amides 8. (C) 1998 Elsevier Science Ltd. AII rights reserved.

  DOI：

  10.1016/s0040-4020(98)00353-6
• 作为产物：
  描述：

  1H-苯并三唑-1-甲醇 、 对氨基苯腈 以 乙醇 为溶剂， 以95%的产率得到N-((1H-benzo[d][1,2,3]triazole)-1-methyl)-4-cyanoaniline
  参考文献：
  名称：

  The preparation of functionalized amines and amides using benzotriazole derivatives and organozinc reagents

  摘要：

  Secondary and tertiary amines 6 are conveniently prepared in good yields by reacting organozinc halides with adducts 4, which are derived from the corresponding amines, aldehydes and benzotriazole. The use of organozinc reagents enables the introduction of nitro, cyano or ester functionalities into amine mainframes. This methodology was also used to prepare functionalized amides 8. (C) 1998 Elsevier Science Ltd. AII rights reserved.

  DOI：

  10.1016/s0040-4020(98)00353-6

文献信息

• 苯并三氮唑衍生物做为RSK2抑制剂的合成及应 用
  申请人：华东理工大学

  公开号：CN102688233B

  公开（公告）日：2016-02-17

  发明涉及苯并三氮唑衍生物的合成及其用途。具体而言，本发明涉及下式II所示的化合物、含有式II化合物的药物组合物及所述化合物在制备治疗或预防RSK2介导的疾病用的药物中的用途：
• Tyrosine Kinase Inhibitors. 3. Structure-Activity Relationships for Inhibition of Protein Tyrosine Kinases by Nuclear-Substituted Derivatives of 2,2'-Dithiobis(1-methyl-N-phenyl-1H-indole-3-carboxamide)
  作者：Gordon W. Rewcastle、Brian D. Palmer、Ellen M. Dobrusin、David W. Fry、Alan J. Kraker、William A. Denny

  DOI：10.1021/jm00039a016

  日期：1994.6

  A series of indole-substituted 2,2'-dithiobis(1-methyl-N-phenyl-1H-indole-3-carboxamides) were prepared and evaluated for their ability to inhibit the tyrosine kinase activity of both the epidermal growth factor receptor (EGFR) and the nonreceptor pp60(v-src) tyrosine kinase. The compounds were synthesized by conversion of appropriate 1-methyloxindoles to 1-methyl-2-indolinethiones with P2S5 followed by subsequent reaction with NaH and phenyl isocyanate and oxidative dimerization of the resulting 2,3-dihydro-N-phenyl-2-thioxo-1H-indole-3-carboxamides. The parent compound and many of the substituted analogues were moderately potent inhibitors of both kinase enzymes, but no clear relationships were seen between substitution on the indole ring and inhibitory activity, While 4-substituted compounds were generally inactive, 5-substituted derivatives with electron-withdrawing groups showed inhibitory activity. However, none of the substituted compounds showed significantly better activity than the unsubstituted parent compound. There was generally a good correlation between activity against the EGFR and pp60(v-src) kinases, but several compounds did show some specificity (>20-fold) of inhibition; 5-Cl and 5-Br derivatives preferentially inhibited pp60(v-src), while the 5-CF3 compound preferentially inhibited EGFR. Selected compounds from the series were found to inhibit the growth of Swiss 3T3 fibroblasts with IC(50)s in the range 2-25 mu M, the most active being 4-substituted derivatives. The compounds inhibited bFGF-mediated protein tyrosine phosphorylation in intact cells more effectively than EGFR- or PDGF-mediated phosphorylation.
• Rewcastle Gordon W., Palmer Brian D., Dobrusin Ellen M., Fry David W., Kr+, J. Med. Chem, 37 (1994) N 13, S 2033-2042
  作者：Rewcastle Gordon W., Palmer Brian D., Dobrusin Ellen M., Fry David W., Kr+

  DOI：——

  日期：——
• The preparation of functionalized amines and amides using benzotriazole derivatives and organozinc reagents
  作者：Alan R. Katritzky、Sonja Strah、Sergei A. Belyakov

  DOI：10.1016/s0040-4020(98)00353-6

  日期：1998.6

  Secondary and tertiary amines 6 are conveniently prepared in good yields by reacting organozinc halides with adducts 4, which are derived from the corresponding amines, aldehydes and benzotriazole. The use of organozinc reagents enables the introduction of nitro, cyano or ester functionalities into amine mainframes. This methodology was also used to prepare functionalized amides 8. (C) 1998 Elsevier Science Ltd. AII rights reserved.