REACTION OF KETENES WITH N,N-DISUBSTITUTED ALPHA-AMINOMETHYLENEKETONES .24. 2H-PYRANO[3,2-D]-1-BENZOXEPIN DERIVATIVES WITH PLATELET ANTIAGGREGATING AND OTHER ACTIVITIES

被引:0
|
作者
LONGOBARDI, M
BARGAGNA, A
MARIANI, E
SCHENONE, P
LOSASSO, C
CENICOLA, ML
DANTONIO, M
MARMO, E
机构
[1] UNIV GENOA,IST SCI FARMACEUT,VIALE BENEDETTO XV 3,I-16132 GENOA,ITALY
[2] UNIV FEDERICO II,FAC MED & CHIRURG,IST FARMACOL & TOSSICOL 1,I-80138 NAPLES,ITALY
来源
FARMACO | 1991年 / 46卷 / 03期
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D O I
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中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The synthesis of some N,N-disubstituted 4-amino-5,6-dihydro-3-phenyl-2H-pyrano[3,2-d]-1-benzoxepin-2-ones by reaction of phenylchloroketene with a series of N,N-disubstituted (E)-4-aminomethylene-3,4-dihydro-1-benzoxepin-5(2H)-ones, followed by dehydrochlorination of the primary adducts with DBN, is described. Some of these compounds showed a platelet antiaggregating activity in vitro slightly superior to that of acetylsalicylic acid, as well as weak local anesthetic and antiinflammatory activities in mice and rats, respectively.
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页码:449 / 460
页数:12
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