发明名称 UN PROCEDIMIENTO PARA LA PREPARACION DE NUEVOS DERIVADOS DE QUINAZOLINA.
摘要 <p>Quinazoline derivatives of the formula …<CHEM>… wherein Ra is hydrogen or alkyl and and q is 2 or 3;… R is hydorgen, hydroxy and alkyl;… Alk is an alkylene chain having from 1 to 4 carbon atoms and Q is a quinazolinyl radical, the 1-, 2-, 3- or 4-position of which is connected with the alkylene side chain, said quinazolinyl radical bearing in one or both of its 2-and 4-positions a carbonyl or thiocarbonyl group, wherein the benzene ring of said quinazolinyl radical is optionally substituted with 1 to 3 substituents each independently selected from the group consisting of halo, alkyl; alkyloxy, trifluoromethyl, nitro and cyano, and wherein the pyrimidino ring of said quinazolinyl radical may be partly or fully saturated, said pyrimidino ring being optionally substituted with 1 to 3 substituents independently selected from the group consisting of alkyl, aryl and aryl(lower alkyl);… wherein said aryl as used in the definition of said Ar and of said Q is a member selected from the group consisting of phenyl, substituted phenyl, thienyl and pyridinyl, wherein said substituted phenyl has from 1 to 3 substituents each independently selected from the group consisting of halo, lower alkyl, lower alkyloxy, trifluoromethyl and amino. These derivatives are serotonin antagagonists. Further are described compounds of the formula …<CHEM>… (Q, Alk and R have the same meaning as above), R8 and R9 being hydrogen, halogen, alkyl, alkoxy, CF3 and amino, having the same activity.</p>
申请公布号 ES487537(D0) 申请公布日期 1980.12.16
申请号 ES19370004875 申请日期 1980.01.08
申请人 JANSSEN PHARMACEUTICA 发明人
分类号 C07D409/14;A61K31/4523;A61K31/505;A61K31/517;A61P9/08;A61P25/02;C07D211/32;C07D239/74;C07D239/80;C07D239/90;C07D239/96;C07D401/06;C07D401/14;C07D405/14;(IPC1-7):07D401/14;61K31/435;61K31/505;61K31/40 主分类号 C07D409/14
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