methyl 4-(3-aminophenylaminomethyl)benzoate | 1202748-45-5

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 英文名称: methyl 4-(3-aminophenylaminomethyl)benzoate
• 英文别名: methyl 4-[(3-aminoanilino)methyl]benzoate
• CAS: 1202748-45-5
• 化学式: C₁₅H₁₆N₂O₂
• 分子量: 256.304
• InChiKey: IIFWPUKRYYOYPH-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.6
• 重原子数：
  19
• 可旋转键数：
  5
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.13
• 拓扑面积：
  64.4
• 氢给体数：
  2
• 氢受体数：
  4

反应信息

• 作为产物：
  描述：

  methyl 4-(3-nitrophenylaminomethyl)benzoate 在 一水合肼 作用下， 以 水 为溶剂， 以85%的产率得到methyl 4-(3-aminophenylaminomethyl)benzoate
  参考文献：
  名称：

  Reductive transformations of Schiff bases in the synthesis of functionally substituted heteroaromatic amines

  摘要：

  Schiff bases synthesized by condensation of 5- and 6-aminoquinolines, 5-amino-2-methylquinoline, nitroanilines, and pyrimidinylaminoanilines with substituted benzaldehydes and pyridinecarbaldehydes were reduced with sodium tetrahydridoborate in acetic acid to obtain the corresponding N-aryl(hetaryl)benzylamines, N-(pyridylmethyl)anilines, and N-(1,2,3,4-tetrahydroquinolyl)benzylamine derivatives. The reduction of arylhetarylimines with hydrazine hydrate in the presence of Raney nickel involved only the azomethine C=N bond, while the nitrogen-containing heteroaromatic ring remained intact. Under analogous conditions, nitrosubstituted Schiff bases and benzyl- and pyridylmethylamines were converted into previously unknown N-(aminobenzyl)quinolinamines and aryl(pyridyl)methyl-substituted phenylenediamines.

  DOI：

  10.1134/s1070428009070148