An efficient route to 3-aryl-substituted quinolin-2-one and 1,8-naphthyridin-2-one derivatives of pharmaceutical interest

被引:28
作者
Mitsos, CA [1 ]
Zografos, AL [1 ]
Igglessi-Markopoulou, O [1 ]
机构
[1] Natl Tech Univ Athens, Sch Chem Engn, Organ Chem Lab, GR-15773 Athens, Greece
关键词
D O I
10.1021/jo0340051
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Reaction of arylacetic ester enolates with 2-alkoxy-4H-3,1-benzoxazin-4-ones offers a short and versatile synthetic route to 3-aryl-4-hydroxyquinolin-2(1H)-ones, through the cyclization of the beta-ketoesters produced. Similar reactions of 4H-pyrido[2,3-d][1,3]oxazin-4-ones with ester enolates afford 1-acyl-4-hydroxy-1,8-naphthyridin-2(1H)-ones in a convenient two-step, one-pot procedure.
引用
收藏
页码:4567 / 4569
页数:3
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