Synthesis of 2-(2-Aminophenyl)-4-arylquinazoline Derivatives by Reaction of 2-Aminoarylbenzimidamides with Isatoic Anhydride
作者:Kamal M. El-Shaieb、Peter G. Jones
DOI:10.1515/znb-2009-0810
日期:2009.8.1
A series of 2-(2-aminophenyl)-4-arylquinazoline derivatives (5a - j), with various 4-substituents, have been synthesized by one-pot cyclization in 66 - 79% yield by heating 2-aminoarylbenzimidamides 3a - j with isatoicanhydride (4). The high yield and simplified workup procedure, in addition to the neutral reaction conditions, are the main advantages of our approach. The structure of the product 5e
通过将 2-氨基芳基苯并亚胺 3a-j 与靛红酸酐 (4)。除了中性反应条件外,高产率和简化的后处理程序是我们方法的主要优点。产物 5e 的结构通过单晶 X 射线结构分析进一步证实 2-(2-氨基苯基)-4-芳基喹唑啉衍生物通过 2-氨基芳基苯并亚胺与靛红酸酐反应合成 2-(2-氨基苯基)-4-芳基喹唑啉衍生物
Synthesis of Benzonaphtho[1,4]Diazepine Derivatives via the Reaction of 2-Aminoarylbenzimidamides with 2,3-Dichloro-1,4-Naphthoquinone
作者:Kamal M. El-Shaieb
DOI:10.3184/030823410x12659615450519
日期:2010.3
A series of (Z)-13-(arylimino)-12,13-dihydro-5H-benzo[e]naphtho[2,3-b][1,4]diazepine-6,11-dione derivatives have been synthesised by one pot cyclisation in good yield via electron donor–acceptor complexes by reacting 2-aminoarylbenzimidamides with 2,3-dichloro-1,4-naphthoquinone. The high yield and simplified workup procedure in addition to the mild and neutral reaction conditions are the main advantages