发明名称 PROCESS
摘要 Acylated pyrido [3,4-e]-as-triazines of the formula (I), <IMAGE> (I) wherein R1 stands for alkyl, alkoxy, haloalkyl, furyl, pyridyl, phenyl, phenyl-(C1-4alkyl) or phyenyl-(C2-4 alkenyl) optionally substituted. R2 stands for hydrogen or a group of the formula R1-CO-, R3 stands for hydrogen, a phenyl group or a naphthy6l group optionally substituted, or a phenyl-(C1-4alkyl) group, pyridyl group or a C1-20alkyl group, and R4 stands for hydrogen or a group of the formula R1-CO-, and R5 forms together with R2 or R4 a valence bond, wherein R2 or R4 taking part in forming said valence bond may not have the above meaning, and pharmaceutically acceptable acid addition salts thereof, which are prepared by reacting a pyrido [3,4-e]-as-triazine of the formula (II) or an acid addition salt thereof <IMAGE> (II) R6 stands for hydrogen, and R5 forms together with Rand R4 a valence bond, with an acylating agent of the formula (III). R1-CO-X (III) The compounds exert favourable effects on the central nervous system, and can be applied primarily as analgesic and antiphlogistic agents.
申请公布号 AU5578180(A) 申请公布日期 1980.08.28
申请号 AU19800055781 申请日期 1980.02.21
申请人 EGYT GYOPGSZERVEGYESZETI GYAR 发明人 PAL BEMKO;GYORGYI KOVANYI;JUDIT TIMAR;MARIA SIGMOND;LUJZA PETOCZ;PETER GOROG;IBOLYA KOSOCZKY;ENIKO SZIRT;HRISZTONE TONCSEV
分类号 A61K31/53;A61P25/04;A61P29/00;C07D471/04 主分类号 A61K31/53
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