Alum catalyzed convenient synthesis of quino[2,3-b][1,5]benzoxazepine α-aminophosphonate derivatives

被引:0
作者
Sonar, Swapnil S. [1 ]
Sadaphal, Sandip A. [1 ]
Shitole, Nana V. [1 ]
Jogdand, Nivrutti R. [1 ]
Shingate, Bapurao B. [2 ]
Shingare, Murlidhar S. [1 ]
机构
[1] Department of Chemistry, Dr. Babasaheb Ambedkar Marathwada University
[2] National Chemical Laboratory
关键词
α-Aminophosphonate; Alum; Quino[2,3-b][1,5]benzoxazepine; Solventfree; Triethyl phosphite;
D O I
10.5012/bkcs.2009.30.8.1711
中图分类号
O6 [化学]; TQ03 [化学反应过程]; TQ02 [化工过程(物理过程及物理化学过程)];
学科分类号
0703 ; 081701 ; 081704 ;
摘要
We have described an efficient synthesis of quino[2,3-b][1,5]benzoxazepine α-aminophosphonate derivatives by the nucleophilic addition of triethyl phosphite to substituted quino[2,3-b][1,5]benzoxazepines promoted by easily available, inexpensive and mild catalyst KAl(SO4)2·12H2O (alum). The reactions proceed smoothly at room temperature under solvent-free reaction conditions and providing high yield of product in very short reaction time.
引用
收藏
页码:1711 / 1714
页数:3
相关论文
共 57 条
[1]  
Quin L.D., Quin G.S., A Guide to Organophosphorus Chemistry, (2000)
[2]  
Corbridge D.E.C., Phosphorus Chemistry, Biochemistry & Technology, (2000)
[3]  
Baylis E.K., Campbell C.D., Dingwall J.G., J. Chem. Soc. Perkin Trans., (1984)
[4]  
Allen M.C., Fuhrer W., Truck B., Wade R., Wood J.M., J. Med. Chem., 32, (1989)
[5]  
Kafraski P., Lejezak B., Phosphorus, Sulfur, Silicon Relat. Elem., 63, (1991)
[6]  
Hirschmann R., Smith A.B., Taylor C.M., Benkovic P.A., Taylor S.D., Yager K.M., Sprengler P.A., Venkovic S.J., Science, 265, (1994)
[7]  
Pokalwar R.U., Hangarge R.V., Maske P.V., Shingare M.S., Arkivoc, 11, (2006)
[8]  
Mccormick J.L., Mckee T.C., Cardellina J.H., Boyd M.R., J. Nat. Prod., 59, (1996)
[9]  
Nadaraj V., Selvi S.T., Sasi R., Arkivoc, 10, (2006)
[10]  
Craig J.C., Person P.E., J. Med. Chem., 14, (1971)