发明名称 PROCEDIMIENTO PARA LA OBTENCION DE QUINAZOLINAS.
摘要 <p>The new title compounds, also useful as intermediates for the prepn. of pharmaceuticals, where acyl includes opt. substd. aliphatic, cycloaliphatic, aromatic and araliphatic acyl, amino includes free amino and opt. substd. hydrocarbylamino, and the quinazoline ring may also be further substd., and esp. compounds (I): (where Ac = 2-7C alkanoyl, R'o = H or alkyl, opt. substd. by halogen, OH, amino, alkylamino, dialkylamino, pyrrolidino, piperidino, opt. C-substd. or containing ring unsatd. at beta-position, piperazino, N-alkyl- or N-hydroxyalkyl piperazino, thiomorpholino, or morpholino, opt. C substd. or alkylphenyl opt. substd. in the ring by halogen, OH, alkoxy, amino, or alkyl and Ro = H, halogen alkyl, CF3 or alkoxy) are prepared by converting an appropriate 6-Y-substd. quinazoline into the desired compound by known methods, where Y is a group replaceable by a convertible into an amino group, with opt. elimination or esp. introduction of other substituents. Pref. Y=NO2 is reduced to -NH2.</p>
申请公布号 ES373399(A1) 申请公布日期 1972.03.16
申请号 ES19990003733 申请日期 1969.11.11
申请人 CIBA, S. A. 发明人
分类号 B63B3/66;C07D239/95;(IPC1-7):07D/;61K/ 主分类号 B63B3/66
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