Free accessResearch articleFirst published online 2006-11
An improved synthesis of reduced 9-arylacridine-1,8-diones from 3-amino-5,5-dimethylcyclohex-2-enone,arylaldehydes and 1,3-dicarbonyl compounds in aqueous medium
An improved and green synthesis of 9-arylacridine-1,8-dione derivatives was accomplished by the reaction of 3-amino-5,5-dimethylcyclohex-2-enone, arylaldehydes and 1,3-dicarbonyl compounds in aqueous medium. Novel unsymmetrical 9-arylacridine-1,8-diones differently substituted at the 3 and 6 positions were obtained by this procedure.
JanisR.A., SilverP.J., and TriggleD.J., Adv. Drug. Res.1987, 16, 309; (b) R. Shan, C. Velazquez and E.E. Knaus, J. Med. Chem. 2004, 41, 254; (c) A.F. Dulhunty, S.M. Curtis, S. Watson, L. Cengia and G. Marco, J. Biol. Chem. 2004, 279, 11853.
2.
MartinN., QuinteiroM., SeoaneC., MoraL., SuarezM., OchoaE., and MoralesA., J. Heterocycl. Chem.1995, 51, 235.
3.
WangX.S., ZhangM.M., ZengZ.S., ShiD.Q., TuS.J., WeiX.Y., and ZongZ.M., Tetrahedron Lett.2005, 46, 7169; (b). X.S. Wang, D.Q. Shi, Y.F. Zhang, S.H. Wang and S.J. Tu, Chin. J. Org. Chem. 2004, 24, 430.
4.
TuS.J., MiaoC.B., GaoY., FengY.J., and FengJ.C., Chin. J. Chem.2002, 20, 703.
5.
LiY.L., ZhangM.M., WangX.S., ShiD.Q., TuS.J., WeiX.Y., and ZongZ.M., J. Chem. Res.2005, 600.